{ "count" : 118585, "data" : [ { "id" : "6a2af78374d8ee00a073d624", "title" : "Clinical Trial Project Manager - Feasibility (Cell Therapy)", "company" : "AstraZeneca", "industry" : "Biopharmaceutical", "salary" : { "min" : 155000.0, "max" : 210000.0, "currency" : "AUD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Clinical Trial Project Manager in Sydney, Australia, adjusted for the biotech industry and manager experience level." }, "location" : "Australia", "locations" : [ "Australia" ], "timestamp" : "2026-06-15T01:18:08.880", "fingerprint" : "d406c4c96298deb6e284e8fe34ed75824b9455004c2722aa4d4f132070a807f4", "source" : "workday", "language" : "en", "applyUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Australia--New-South-Wales/Clinical-Trial-Project-Manager---Feasibility--Cell-Therapy-_R-253736-1", "externalId" : "R-253736", "industryFunction" : { }, "locationPoint" : "-25.2744,133.7751", "structuredLocations" : [ { "city" : "Sydney", "country" : "Australia", "continent" : "oc", "source" : "llm", "workMode" : "hybrid", "geo" : "-33.8698439,151.2082848" }, { "city" : "Melbourne", "country" : "Australia", "continent" : "oc", "source" : "llm", "workMode" : "hybrid", "geo" : "-37.8142454,144.9631732" } ], "locationText" : "Sydney, Australia; Melbourne, Australia", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "technicalSkills" : "Veeva Clinical Vault", "professionalSkills" : [ "Site strategy", "Operational readiness", "Study design", "Site selection", "Recruitment baselines", "Recruitment strategies", "Retention strategies", "Delivery plans", "Risk mitigations", "Feasibility responses", "Knowledge transfer" ], "hardSkillsList" : [ "Clinical trial feasibility", "Country feasibility", "Site feasibility", "Investigator networks", "Forecasting" ], "hardSkills" : [ { "name" : "Clinical trial feasibility", "level" : "intermediate" }, { "name" : "Country feasibility", "level" : "intermediate" }, { "name" : "Site feasibility", "level" : "intermediate" }, { "name" : "Investigator networks", "level" : "intermediate" }, { "name" : "Forecasting", "level" : "intermediate" } ], "majorSkills" : "Clinical trial feasibility, Site strategy, Cell therapy", "majorSkillsList" : [ "Clinical trial feasibility", "Site strategy", "Cell therapy" ], "coreResponsibilities" : "Lead country feasibility, Provide feasibility inputs, Provide feasibility timelines, Analyse country landscape, Analyse standard of care, Analyse competitive activity, Inform study design, Inform site selection, Inform recruitment baselines, Build investigator networks, Maintain investigator networks, Build site networks, Maintain site networks, Conduct on-site visits, Assess capability for studies, Develop recruitment strategies, Develop retention strategies, Translate feasibility insights, Mitigate risks, Champion best practice, Provide feasibility responses, Provide knowledge transfer", "teamCollaboration" : "Regional feasibility leaders; Global feasibility leaders; Cell Therapy Field Clinical Advisers; Patient Operations; Clinical Research Associates; Study teams; Matrix teams", "projectManagementSkills" : [ "Study planning", "Feasibility planning" ], "domainKnowledge" : "Cell therapy; Complex modalities; Early-phase studies; First-in-human studies; Oncology; Gene therapy; Immunology; Autoimmune therapeutic areas; Rheumatoid arthritis; Lupus; Multiple sclerosis", "domainList" : [ "cell-therapy", "complex-modalities", "early-phase-studies", "first-in-human-studies", "oncology", "gene-therapy", "immunology", "autoimmune-therapeutic-areas", "rheumatoid-arthritis", "lupus", "multiple-sclerosis" ], "domainSpecificKnowledge" : [ "Cell therapy", "Complex modalities", "Early-phase studies", "First-in-human studies", "Oncology", "Gene therapy", "Immunology", "Autoimmune therapeutic areas", "Rheumatoid arthritis", "Lupus", "Multiple sclerosis" ], "toolProficiency" : [ "Veeva Clinical Vault" ], "communicationSkills" : "Communication skills", "specialRequirements" : "30-40% travel", "qualificationsBasic" : "Bachelor's degree in relevant field, 5+ years clinical development experience, Country-level feasibility experience, Patient recruitment planning experience, Oncology experience, Complex modalities experience, Early-phase studies experience, First-in-human studies experience, Lead complex study feasibility activities, Lead site start-up activities, Stakeholder management skills, Communication skills, Knowledge of ICH/GCP, Knowledge of Australian regulations, Ability to travel within Australia", "qualificationsPreferred" : "Experience with CROs, Experience with academic groups, Experience with Key Opinion Leaders, Exposure to immunology therapeutic areas, Exposure to autoimmune therapeutic areas, Feasibility in non-oncology settings, Experience in regional matrix teams, Experience in global matrix teams, Influencing across functions, Adapting to ambiguity", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "Do you have expertise in clinical trial feasibility, and a passion for delivering groundbreaking therapies to patients? Would you like to apply your experience toward building feasibility and site strategy on a national scale, in a science-led organization delivering life-changing medicines? Then AstraZeneca might be the one for you! ## **About AstraZeneca** AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of diseases in four therapy areas – Oncology; Cardiovascular, Renal and Metabolism (CVRM); Respiratory & Immunology (R&I); and Rare Disease. AstraZeneca Australia has worked for over 60 years to deliver the best value to patients. We advance science to develop life-changing medicines. As part of a new, fast‑growing global cell therapy team, we are building the frameworks, networks and capabilities needed to accelerate delivery of novel, complex therapies to patients. Reporting to the local Senior Director for Cell Therapy Clinical Trials, you will partner with regional and global feasibility leaders as Australia’s expert on site landscape, investigator networks and operational readiness, proactively mapping new therapeutic areas and centres, delivering actionable insights, and helping shape cell therapy ways of working. This is full time, permanent role can be based in Sydney or Melbourne, working remotely with regular travel to sites across Australia and head office in Sydney. ## **What you’ll do** * Lead end‑to‑end country feasibility for internally delivered studies, providing a single point of contact for Australian feasibility inputs and timelines. * Analyse country landscape, standard of care and competitive activity to inform optimal study design, site selection and realistic recruitment baselines. * Build and maintain investigator and site networks across Australia, conducting on‑site visits to assess capability for complex, early‑phase and first‑in‑human studies. * Develop and socialise country‑specific and site‑specific recruitment and retention strategies, aligned to patient needs, regulatory requirements and study objectives. * Partner with Cell Therapy Field Clinical Advisers, Patient Operations and Clinical Research Associates to translate feasibility insights into delivery plans and risk mitigations. * Champion best practice use of planning and analytics platforms and providing high‑quality, timely feasibility responses and knowledge transfer to study teams. ## **Essential Requirements:** * Bachelor’s degree in a relevant field (e.g., life sciences, healthcare) * Substantial experience (approximately 5+ years) in clinical development within the pharmaceutical or biotechnology sector, including country‑level feasibility and patient recruitment planning. * Experience in oncology and/or complex modalities (e.g., cell therapy, gene therapy) and early‑phase or first‑in‑human studies. * Proven track record leading complex study feasibility or site start‑up activities, with strong stakeholder management and communication skills. * Sound knowledge of ICH/GCP and relevant Australian regulations. * Demonstrated ability to travel within Australia to visit sites and collaborators as required (approximately 30–40% travel). * Proficiency with feasibility, forecasting and study planning digital platforms (eg. Veeva Clinical Vault). ## **Desirable for the role:** * Experience working with Clinical Research Organisations, academic groups and Key Opinion Leaders to shape site and investigator engagement. * Exposure to immunology or autoimmune therapeutic areas (e.g., rheumatoid arthritis, lupus, multiple sclerosis) and feasibility in non‑oncology settings. * Experience operating in regional or global matrix teams, influencing across functions and adapting to ambiguity in a scaling organisation. ## **Why AstraZeneca?** At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. ## **So, what’s next!** Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you. Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours - apply now! ## **Guidance on AI use:** We support you using AI tools responsibly in the recruitment process so you can be at your best and showcase your knowledge, skills and abilities. Review our guide to help you do this: ## **Where can I find out more?** * **Visit our Global Website**** _-_**[**_https://www.astrazeneca.com/_**](https://www.astrazeneca.com/) * **Follow AstraZeneca on LinkedIn**[** _https://www.linkedin.com/company/1603/_**](https://www.linkedin.com/company/1603/) * **Follow us on Instagram**** _–_**[** _https://www.instragram.com/astrazeneca/_**](https://www.instragram.com/astrazeneca/) AstraZeneca in Australia has been formally recognised as an Employer of Choice for Gender Equality by the Workplace Gender Equality Agency (WGEA) and as a Gold Tier Employer within the Australian Workplace Equality Index (AWEI). Visit our ANZ Careers Page - [www.astrazeneca.com.au/careers.html](https://www.astrazeneca.com.au/careers.html) to learn more about our commitment to fostering a flexible, diverse, and inclusive environment. We recognise that any recruitment process may present challenges, if there is anything we can do to make our recruitment process more accessible for you, please let us know via this [Form](https://forms.office.com/Pages/ResponsePage.aspx?id=o4mOr6zZL0KtBsxOtCFDFDlQbNTPZApBlQh8e2oSY3VUNklNUDhIQk45VkdJTUxVOVNFMjFKMjdXWiQlQCN0PWcu) **Date Posted** 10-June-2026 **Closing Date** 09-July-2026 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.", "summaryDescription" : "Clinical Trial Project Manager - Feasibility (Cell Therapy) at AstraZeneca. Skills: Clinical trial feasibility, Site strategy, Cell therapy. Lead country feasibility. Provide feasibility inputs", "postedDate" : "2026-06-11T04:47:31.977", "createdAt" : "2026-06-12T04:47:31.879", "lastUpdated" : "2026-06-15T01:18:08.880", "ingestTimestamp" : "2026-06-12T04:47:31.879", "mongoId" : "6a2af78374d8ee00a073d624", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Australia--New-South-Wales/Clinical-Trial-Project-Manager---Feasibility--Cell-Therapy-_R-253736-1", "salaryBand" : "150k-200k", "hasSalary" : false, "allSkills" : [ "Clinical trial feasibility", "Country feasibility", "Site feasibility", "Investigator networks", "Forecasting", "Site strategy", "Cell therapy", "Operational readiness", "Study design", "Site selection", "Recruitment baselines", "Recruitment strategies", "Retention strategies", "Delivery plans", "Risk mitigations", "Feasibility responses", "Knowledge transfer", "Study planning", "Feasibility planning", "Complex modalities", "Early-phase studies", "First-in-human studies", "Oncology", "Gene therapy", "Immunology", "Autoimmune therapeutic areas", "Rheumatoid arthritis", "Lupus", "Multiple sclerosis", "Veeva Clinical Vault" ], "skillCount" : 30, "jobCategory" : "engineering", "seniorityLevel" : "manager", "dataQualityScore" : 1.0, "_score" : 1980.5265, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biopharmaceutical" }, { "id" : "6a308763f292fd229c0887a4", "title" : "Clinical Trial Manager / Associate Clinical Trial Manager", "company" : "ClinChoice", "salary" : { "min" : 95000.0, "max" : 145000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Clinical Trial Manager in the United States, adjusted for mid-seniority and the biotech industry." }, "location" : "United States ", "locations" : [ "United States" ], "timestamp" : "2026-06-16T12:20:07.242", "fingerprint" : "3fb43a822fe7bf18678448f6e62bbd872c977735382e496f4e72ffdfbb159e29", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/clinchoice/jobs/4898549101", "externalId" : "4898549101", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "hybrid" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceLevel" : "Manager", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "ClinChoice is seeking a Clinical Trial Manager / Associate Clinical Trial Manager to join one of our sponsor partners, a Boston-based biotech company focused on CNS disorders. This is a direct-hire, hybrid position requiring three days per week in the office. In this role, you will partner closely with Clinical Operations leadership to support the planning and execution of global clinical trials across multiple indications. It is a highly visible, hands-on opportunity with significant impact on study delivery and operational success. The ideal candidate will have 5+ years of clinical operations experience in biotech or pharma, with a strong background managing outsourced global Phase I–III clinical trials and supporting study start-up activities. They will be highly organized, collaborative professional with expertise in CRO/vendor oversight, trial execution, GCP compliance, and cross-functional coordination to support the successful delivery of a global Phase III study. ClinChoice is a global full-service CRO with a strong focus on quality and professional development. As a client-facing role, we are looking for confident candidates with the ability to work independently while establishing a high-trust environment with their client counterparts. Main Job Tasks and Responsibilities: Provide support to the Clinical Operations Lead (COL) in the planning, execution, and oversight of a global phase 3 clinical trial from study start-up to close-out. Support the development, review and tracking of study-related documents (protocols, ICFs, investigative brochure, monitoring visit reports, etc.) with cross functional team collaboration. Support start-up activities to help accelerate country and site activations. Oversee CRO and vendors, monitor performance metrics, and ensure timely and high-quality deliverables. Track study timelines, enrollment, protocol deviations, data trends, and sample management in partnership with CRO and internal stakeholders. Maintain and organize trial documentation (e.g., TMF/eTMF oversight, trackers, meeting minutes) ensuring that study documentation is in a continuous state of inspection readiness. Contribute to inspection readiness activities and ensure compliance with GCP and SOPs. Help identify and resolve site risks and/or issues to foster positive site relationships. Coordinate internal team meetings and participate in cross-functional study meetings. Proactively communicate study updates with key internal and external stakeholders. Education, Experience and Skills: The Application Process Bachelor’s degree is preferably in life sciences or healthcare related field. 5+ years of clinical operations experience within the biotech or pharma industry required Experience managing outsourced global clinical trials across Phase I–III. Prior involvement in study start-up activities strongly preferred Solid understanding of GCP, ICH guidelines, and the clinical development process. Experience with clinical trial management systems (CTMS), eTMF, and other operational tools. Ability to multitask and flex across projects as priorities and deadlines shift. Highly organized with excellent communication and interpersonal skills. Strong attention to detail and ability to multitask in a dynamic, fast-paced setting. A collaborative team player that takes initiative. Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical devices, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key Words: Clinical Trial Manager, Associate Clinical Trial Manager, Clinical Trial Management, Global, Clinical Study Management, Clinical Trials, Phase III Studies, CRO Oversight, Study Start-Up, Vendor Management, TMF, GCP/ICH Compliance, eTMF/CTMS, Clinical Operations, Site Activation, Inspection Readiness, Risk Management, Cross-Functional Collaboration, Protocol Deviations, Enrollment Management, Biotech/Pharma, CNS, Trial Execution. #LI-VH #LI-Hybrid #Clinical Trial Manager # Permanent", "summaryDescription" : "Clinical Trial Manager / Associate Clinical Trial Manager at ClinChoice", "postedDate" : "2026-06-16T01:21:02.433", "createdAt" : "2026-06-16T01:21:02.433", "lastUpdated" : "2026-06-16T12:20:07.242", "ingestTimestamp" : "2026-06-16T01:21:02.433", "mongoId" : "6a308763f292fd229c0887a4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 145000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 1379.9955, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c958974d8ee00a098d54e", "title" : "Clinical Trial Manager/Sr Clinical Trial Manager", "company" : "Erasca", "industry" : "Biotech", "salary" : { "min" : 7500000.0, "max" : 1.2E7, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimation is based on the US market baseline for a Senior Clinical Trial Manager in the Biotech industry, adjusted for seniority and remote work." }, "location" : "Remote", "locations" : [ "Remote", "San Diego", "California", "United States" ], "timestamp" : "2026-06-15T10:14:23.389", "fingerprint" : "c975d251af2caa4429c4423c0496abc8f5007b5b44d7edf8823037316a85b7eb", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/erasca/jobs/7767584003", "externalId" : "7767584003", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "experienceLevel" : "Manager", "technicalSkills" : "Electronic data capture, Data management software", "professionalSkills" : [ "Trial management", "Resource planning", "Budget management", "Contract negotiation", "Vendor management", "Cross-functional coordination", "Process management", "Continuous improvement", "Stakeholder management" ], "hardSkillsList" : [ "Clinical trial execution", "Clinical trial management", "Clinical operations" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Clinical trial execution", "level" : "intermediate" }, { "name" : "Clinical trial management", "level" : "intermediate" }, { "name" : "Clinical operations", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Clinical trial management, Oncology indications, Vendor management", "majorSkillsList" : [ "Clinical trial management", "Oncology indications", "Vendor management" ], "coreResponsibilities" : "Manage global clinical trials, Recruit global study sites, Foster relationships with study investigators, Participate in site selection, Participate in vendor selection, Participate in site qualification, Participate in vendor qualification, Participate in site activation, Develop Requests-for-Proposals, Assist in vendor selection efforts, Assist in review vendor contracts, Assist in negotiation vendor contracts, Assist in review study site agreements, Assist in negotiation study site agreements, Manage study vendors, Monitor trial progress, Track trial enrollment, Track clinical trial material inventory, Review monitoring visit reports, Assist in packaging clinical trial material, Assist in labeling clinical trial material, Assist in distribution clinical trial material, Monitor biological samples, Track biological samples, Provide progress updates to management, Provide progress updates during meetings, Assist in departmental budgeting, Assist in accruals, Assist in projections, Assist in development protocols, Assist in development consent forms, Assist in development IRB/EC materials, Assist in development trial documents, Assist in development Clinical SOPs, Prepare study materials, Review study materials, Approve study materials, Assist in electronic case report form design, Assist in electronic case report form development, Assist in IRT design, Assist in IRT development, Participate in data cleaning, Develop appropriate data outputs, Fulfill needs of other Erasca departments, Provide leadership to team members, Perform duties in keeping with core values, Perform duties in keeping with policies, Perform duties in keeping with regulations", "teamCollaboration" : "Global multi-disciplinary teams; Program team meetings; Other Erasca departments", "projectManagementSkills" : [ "Clinical trial management", "Project management", "Priority management" ], "domainKnowledge" : "Oncology indications; RAS/MAPK pathway; ICH-GCP; FDA regulations; Regulatory agency requirements", "domainList" : [ "oncology-indications", "ras-mapk-pathway", "ich-gcp", "fda-regulations", "regulatory-agency-requirements" ], "domainSpecificKnowledge" : [ "Oncology indications", "RAS/MAPK pathway", "ICH-GCP", "FDA regulations", "Regulatory agency requirements" ], "toolProficiency" : [ "IRT", "ECG", "Electronic data capture" ], "communicationSkills" : "Oral communication; Written communication", "documentationSkills" : "Clinical documentation; Protocols; Consent forms; IRB/EC materials; CRFs; Patient diaries; Drug accountability forms; Study manuals; Investigator manuals; Project plans; Monitoring reports; SOPs", "continuousLearning" : "Learning orientation", "qualificationsBasic" : "5 years of relevant experience, 7 years of relevant experience, ICH-GCP guidelines experience, US and ex-US regulations experience, Electronic data capture experience, Data management software experience, Clinical Research Associates management experience, Reviewing monitoring trip reports experience", "qualificationsPreferred" : "Undergraduate degree in life sciences", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer. The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation, and management of clinical studies from concept to completion. The position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out, including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources, budgets, contracts, and timelines. Essential Duties and Responsibilities: Manage global clinical trials (Phase 1-3) in oncology indications, ensuring that studies are carried out in accordance with the clinical development plan, ICH-GCP, and FDA/other regulatory agency requirements. Recruit global study sites and foster relationships with study investigators. Participate in the process of site and vendor selection, qualification, and activation. Develop Requests-for-Proposals and assist in vendor selection efforts. Assist in review and negotiation of vendor contracts and study site clinical trial agreements. Manage study vendors (e.g., CRO, IRT, laboratories, core ECG/imaging). Monitor the progress of trials, including enrollment and clinical trial material inventory. Review monitoring visit reports for completeness and adherence to the annotations. Assist in packaging/labeling/distribution of clinical trial material. Monitor and track biological samples for applicable analyses. Provide progress updates to management and during program team meetings. Assist in departmental budgeting, including accruals and projections. Assist in development of protocols, consent forms, IRB/EC materials, and other trial documents. Assist in development of Clinical SOPs. Prepare/review/approve study materials such as CRFs, patient diaries, drug accountability forms, study and investigator manuals, project plans, and monitoring reports. Assist in electronic case report form design and development.  Assist in IRT design and development. Participate in data cleaning activities and developing appropriate data outputs. Understand and help fulfill the needs of other Erasca departments (e.g., Finance, Research). Provide leadership and mentoring of other Clinical team members. Perform all duties in keeping with the Company’s core values, policies and all applicable regulations. Required Education, Experience and Attributes: Preferred undergraduate degree in life sciences or professions (pharmacy, medicine, nursing, or other allied health sciences). For Clinical Trial Manager, at least 5 years of relevant experience in oncology clinical operations in pharmaceutical company or CRO including trial set-up, monitoring, and close-out of US and non-US trials at all phases of pre-NDA clinical research (Phases 1-3). For Senior Clinical Trial Manager, at least 7 years of relevant experience required. Demonstrated excellence in trial management skills, with track record of successfully managing multiple projects, trials, and priorities. Experience with managing study vendors (e.g., CRO, IRT, laboratories, core ECG/imaging). Ability to work well with global, multi-disciplinary teams. Experience in practical knowledge and implementation of ICH-GCP guidelines and US and ex-US regulations. Experience with electronic data capture and data management software. Experience in the management of Clinical Research Associates. Excellent oral and written communication skills. Experience with reviewing monitoring trip reports Must be able to thrive in an entrepreneurial, fast-paced, and dynamic work environment. Must be organized and be able to communicate effectively. Must be a self-starter. Strong learning orientation, curiosity, and commitment to science and patients. The anticipated salary range for this position is $145,000 to $190,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etcetera. In addition to base salary, the hired applicant will be eligible to receive an annual bonus and an equity grant at hire and annually in the form of the option to purchase stock in the future for a specified price. Along with our casual, collaborative, and fun work and the chance to make your mark in our mission to erase cancer, Erasca offers a comprehensive and competitive benefits package that includes: Paid Time Off, Holiday, and Sick Leave, Medical, Dental and Vision Plans, Short- and Long-Term Disability, Basic and Voluntary Life/AD&D Coverage, Flexible Spending Accounts (FSA, HSA, and Commute), Critical Illness and Accident Coverage, Pet Insurance, Employee Assistance Program, 401(k) Plan with Erasca contribution, and the opportunity to participate in an Employee Stock Purchase Program. Erasca, Inc., is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of sex , race, religion, national origin, ancestry, physical or mental disability, protected medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law or ordinance or regulation.", "summaryDescription" : "Clinical Trial Manager/Sr Clinical Trial Manager at Erasca. Skills: Clinical trial management, Oncology indications, Vendor management. Manage global clinical trials. 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We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem. We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection. With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business. Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. The opportunity: Program Manager - Clinical Trial Operations As a Program Manager, your main responsibility is to ensure (global) access to clinical trials via smooth running digital patient recruitment and pre-screening programs. The aim of our patient recruitment programs is to (1) increase patients’ and physicians’ clinical trial awareness and understanding, (2) pre-screen patients to assess their potential clinical trial eligibility, (3) provide high-quality patient referrals to clinical trial sites and 4) ultimately boost patient enrollment rates. You will serve as the first point of contact for pharmaceutical and biotech partners, providing end‑to‑end oversight of all patient recruitment program activities. You will ensure timely and high‑quality delivery of patient recruitment programs by coordinating stakeholders and driving effective, compliant patient engagement from first contact to site referral and enrollment. You will be supported by cross-functional experts across Patient Navigation, Medical Community, Marketing, Product and Engineering. Geographic Requirement: To ensure seamless collaboration with our teams, applicants must reside within the EST or CST time zones. WHAT YOU'LL DO IN THIS ROLE: - Be the primary contact person for our BioPharma clients and internal stakeholders for the patient recruitment programs under your responsibility - Be responsible for the onboarding and launch of new programs, including overseeing the development of patient recruitment materials (e.g., clinical trial landing pages with pre-screening questionnaires) - Ensure a smooth-running program and insight-driven reporting - Keep (financial) oversight of the program and manage all the ongoing activities and communication - Create detailed timelines including deliverables, milestones and objectives and ensure that deadlines are being met - Develop strong relations and trust with all stakeholders and keep them up to date on the progress of your programs - Achieve and maintain high customer satisfaction - Develop and advise on solutions to tackle operational issues along with relevant subject matter experts - Contribute to improving our patient recruitment and pre-screening processes and strategies - Support overall myTomorrows program performance and operations, as needed. WHAT YOU BRING TO THE TABLE: - University degree in Life Sciences/Healthcare (preferred) - 2+ years of trial / project management experience within the pharmaceutical industry / CROs - Thorough understanding of clinical research and clinical trial patient recruitment - Proven ability to manage complex, cross-functional programs with multiple internal and external stakeholders, ensuring timely delivery and budget oversight - Experience leading client-facing programs, including managing expectations, communicating progress, and serving as a trusted partner to Sponsors and sites - Strong communication and diplomatic skills, with the ability to navigate sensitive situations, balance stakeholder interests, and maintain productive long‑term relationships - A commercial mindset, with the ability to understand commercial drivers, track program financials, and contribute to strategic decision‑making - Basic understanding of how web pages and search engine ads function, to ensure a smooth collaboration with the Marketing and Product & Engineering teams - A good eye for detail; thinking in processes/operations comes natural to you - Able to prioritize, analyze issues, optimize processes and find / recommend alternative solutions - Excellent verbal and written communication skills in English WHAT SUCCESS IN THE FIRST 6 MONTHS LOOKS LIKE: - At least one-two patient recruitment program launched on time, operating smoothly. - A sustained flow of high-quality, pre‑screened referrals meeting protocol-specific criteria, with clear conversion from inquiry to enrollment. - Strong client relationships, evidenced by NPS > 50 and no escalations. - Seamless collaboration with other teams incl. Patient Navigation, Medical Community, Marketing, Product & Engineering. WHAT WE OFFER: - Impactful work that helps patients gain access to potentially lifesaving treatments. - International work environment, scale-up energy and a flat organizational structure that encourages creativity and accountability. - Competitive salary, annual performance bonus and an Employee Stock Option Plan. - Great career development opportunities in a fast-growing company. - Learning and development budget alongside internal knowledge sharing sessions. - Attractive pension plan, full premium covered by myTomorrows. - Hybrid working model. - Policies to support working parents. - Healthy lunch at the thriving Amsterdam office. - Unlimited access to professional guidance by certified psychologists via OpenUp - Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration! Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that. ", "summaryDescription" : "Program Manager, Clinical Trial Operations at myTomorrows", "createdAt" : "2026-06-14T19:28:16.237", "lastUpdated" : "2026-06-16T04:24:55.804", "ingestTimestamp" : "2026-06-14T19:28:16.237", "mongoId" : "6a2c8cf574d8ee00a0977c58", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 125000, "salaryAnnualMax" : 175000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 1004.73846, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c5f4974d8ee00a08eab1a", "title" : "Senior Clinical Trial Manager", "company" : "Recursion", "industry" : "Biopharmaceutical", "salary" : { "min" : 175000.0, "max" : 245000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Clinical Trial Manager in New York, USA, adjusted for biotech industry and company size." }, "location" : "New York, New York", "locations" : [ "New York", "New York", "Salt Lake City", "Utah" ], "timestamp" : "2026-06-15T00:14:37.215", "fingerprint" : "534fe49dbfbc159cbce62a8ea8c2872cf2a02a183bd2bfcb18a4b492c721e393", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/recursionpharmaceuticals/jobs/8001436", "externalId" : "8001436", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New York", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7127281,-74.0060152" } ], "locationText" : "New York, New York, United States", "minimumEducation" : "Bachelor's", "experienceMinYears" : 6, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Smartsheet, CTMS, Project management tools, Document management systems", "professionalSkills" : [ "Clinical trial management", "Clinical operations", "Relationship management" ], "hardSkillsList" : [ "Trial execution", "Timeline management", "Deliverable tracking", "Process improvements" ], "softSkillsList" : [ "Adaptability", "Problem-solving" ], "hardSkills" : [ { "name" : "Trial execution", "level" : "intermediate" }, { "name" : "Timeline management", "level" : "intermediate" }, { "name" : "Deliverable tracking", "level" : "intermediate" }, { "name" : "Process improvements", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Adaptability" }, { "name" : "Problem-solving" } ], "majorSkills" : "Clinical trial management, Clinical operations, Regulatory compliance", "majorSkillsList" : [ "Clinical trial management", "Clinical operations", "Regulatory compliance" ], "coreResponsibilities" : "Support Clinical Project Manager, Manage clinical trial activities, Track clinical trial timelines, Track clinical trial deliverables, Engage clinical CRO partners, Build relationships with trial partners, Identify operational improvements, Identify process improvements, Contribute to development portfolio", "teamCollaboration" : "Cross-functional study teams; Clinical Operations team; Diverse internal stakeholders; External stakeholders", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Drug discovery; Automated cell biology; High-dimensional data; Diverse data sets; Sophisticated analytics; Biopharmaceutical industry; Oncology; Rare disease; FDA regulations; ICH guidelines; GCP regulations", "domainList" : [ "drug-discovery", "automated-cell-biology", "high-dimensional-data", "diverse-data-sets", "sophisticated-analytics", "biopharmaceutical-industry", "oncology", "rare-disease", "fda-regulations", "ich-guidelines", "gcp-regulations" ], "domainSpecificKnowledge" : [ "Drug discovery", "Automated cell biology", "High-dimensional data", "Diverse data sets", "Sophisticated analytics", "Biopharmaceutical industry", "Oncology", "Rare disease", "FDA regulations", "ICH guidelines", "GCP regulations" ], "toolProficiency" : [ "Smartsheet", "CTMS", "Project management tools", "Document management systems" ], "communicationSkills" : "Interpersonal skills", "problemSolvingSkills" : "Problem-solving abilities", "specialRequirements" : "Willingness to travel", "outcomesObjectives" : "Deliver transformative medicines", "qualificationsBasic" : "Bachelor's degree or equivalent experience, 6+ years of experience in clinical operations, 2+ years experience as regional CTM, Early phase oncology/rare disease experience, Working knowledge of FDA regulations, Working knowledge of ICH guidelines, Working knowledge of GCP regulations", "qualificationsPreferred" : "Monitoring experience, Automating trial activity tracking, Smartsheet or other CTMS/tracking tools, Experience at a Sponsor or CRO", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Your work will change lives. Including your own. The Impact You’ll Make Recursion is at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics. We are seeking a highly motivated, skilled, and adaptable Clinical Trial Manager within our Clinical Operations team who will manage the conduct and execution of one or more clinical trials from study start-up to study closure in close collaboration with the Clinical Project Manager and/or Associate Director/Director of Clinical Operations. In this role, you will: Support the Clinical Project Manager in the execution of trial operations across diverse therapeutic areas to deliver transformative, new medicines to patients Manage and track clinical trial activities, timelines, and deliverables Engage and build relationships with clinical CRO and trial partners to support the successful execution of clinical trial activities Proactively identify opportunities for operational and process improvements within the Clinical Operations team Contribute to the advancement of the Recursion development portfolio The Team You’ll Join Reporting to an Associate Director/Director of Clinical Operations, you will be an essential member of the Clinical Operations team within Development and work closely with cross-functional study teams. You will impact all phases of Development clinical trials. The team is dedicated to ensuring operational excellence across our clinical programs. The Experience You’ll Need Bachelor’s degree or equivalent experience 6+ years of experience in a clinical operations role in the biopharmaceutical industry, with at least 2+ years experience as a regional CTM or similar operations role required Preferred experience: monitoring experience, automating trial activity tracking through Smartsheet or other CTMS/tracking tools Early phase (Phase 1, 2) oncology and/or rare disease experience at a Sponsor or CRO is required Strong working knowledge of FDA, ICH, GCP regulations and guidelines Effective collaboration in a fast-paced team environment Excellent interpersonal and communication skills, and an understanding of principles of relationship management across diverse internal and external stakeholders Detail-oriented with effective organizational and problem-solving abilities. Experience in managing multiple priorities and able to accomplish tasks within a timeframe, setting milestones to meet deadlines and to achieve goals Proficient in using various software applications related to clinical trials, such as, but not limited to: smartsheet, clinical trial management systems, project management tools, document management systems, and electronic data capture tools Willingness to travel to sites, conferences, and/or Recursion offices (NYC and SLC) as needed Working Location & Compensation: This position is open to both remote and hybrid models. The hybrid position would be office-based at our London, England office near King's Cross. Employees are expected to work in the office at least 50% of the time. Relocation support can be provided for candidates not local to either geographical location. At Recursion, we believe that every employee should be compensated fairly. Based on the skill and level of experience required for this role, the estimated current annual base range for this role is £62,400 to £84,000. You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package. #LI-ES1 #LI-REMOTE The Values We Hope You Share: We act boldly with integrity. We are unconstrained in our thinking, take calculated risks, and push boundaries, but never at the expense of ethics, science, or trust. We care deeply and engage directly. Caring means holding a deep sense of responsibility and respect - showing up, speaking honestly, and taking action. We learn actively and adapt rapidly. Progress comes from doing. We experiment, test, and refine, embracing iteration over perfection. We move with urgency because patients are waiting. Speed isn’t about rushing but about moving the needle every day. We take ownership and accountability. Through ownership and accountability, we enable trust and autonomy—leaders take accountability for decisive action, and teams own outcomes together. We are One Recursion. True cross-functional collaboration is about trust, clarity, humility, and impact. Through sharing, we can be greater than the sum of our individual capabilities. Our values underpin the employee experience at Recursion. They are the character and personality of the company demonstrated through how we communicate, support one another, spend our time, make decisions, and celebrate collectively. More About Recursion Recursion (NASDAQ: RXRX) is a clinical-stage TechBio company decoding biology to radically improve lives. Recursion is advancing a portfolio of differentiated investigational medicines across its wholly owned and partnered pipeline in oncology, rare disease, neuroscience, immunology, and other therapeutic areas with significant unmet need. Enabling its mission is the Recursion OS, an AI-native, end-to-end drug discovery and development platform integrating biology, chemistry, and clinical development into a unified intelligence system. Powered by proprietary multimodal data, purpose-built AI models, and bilingual teams fluent in both science and AI, the Recursion OS is designed to translate complex science into medicines that matter — faster, better, and at scale — for patients who are waiting. Recursion’s platform infrastructure is anchored in Salt Lake City, Utah and Milton Park, Oxfordshire, where its automated biology and chemistry laboratories generate proprietary data at industrial scale. Recursion also maintains offices in New York, Montréal, and London, three global hubs for talent and leadership at the intersection of AI and scientific innovation. Learn more at www.recursion.com, or connect on X and LinkedIn. Recursion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable federal, state, local, or provincial human rights legislation. Accommodations are available on request for candidates taking part in all aspects of the selection process. Recruitment & Staffing Agencies: Recursion Pharmaceuticals and its affiliate companies do not accept resumes from any source other than candidates. The submission of resumes by recruitment or staffing agencies to Recursion or its employees is strictly prohibited unless contacted directly by Recursion’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Recursion, and Recursion will not owe any referral or other fees. Our team will communicate directly with candidates who are not represented by an agent or intermediary unless otherwise agreed to prior to interviewing for the job.", "summaryDescription" : "Senior Clinical Trial Manager at Recursion. Skills: Clinical trial management, Clinical operations, Regulatory compliance. Support Clinical Project Manager. 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CROs; Study vendors; Clinical Data Management; Cross functional team members; External collaborators; Research and development groups", "projectManagementSkills" : [ "Study timelines", "Study costs", "Quality metrics" ], "domainKnowledge" : "Clinical Trial SOPs; FDA Regulations; ICH-GCPs; Clinical trials; Regulated environment; PHI privacy; Human Subjects Protection; GCP; Cell-free DNA testing; Oncology; Women's health; Organ health; Genetic testing; Genetic diagnostics", "domainList" : [ "clinical-trial-sops", "fda-regulations", "ich-gcps", "clinical-trials", "regulated-environment", "phi-privacy", "human-subjects-protection", "gcp", "cell-free-dna-testing", "oncology", "women-s-health", "organ-health", "genetic-testing", "genetic-diagnostics" ], "domainSpecificKnowledge" : [ "Clinical Trial SOPs", "FDA Regulations", "ICH-GCPs", "Clinical trials", "Regulated environment", "PHI privacy", "Human Subjects Protection", "GCP", "Cell-free DNA testing", "Oncology", "Women's health", "Organ health", "Genetic testing", "Genetic diagnostics" ], "toolProficiency" : [ "MS Word", "MS Excel", "MS PowerPoint" ], "communicationSkills" : "Written communication; Oral communication", "documentationSkills" : "Protocol preparation; Informed consent preparation; Monitoring plans development; CRFs completion; TMF maintenance; Clinical report preparation; Completion guidelines; Data listings; Study reports", "problemSolvingSkills" : "Identify problems; Identify solutions", "specialRequirements" : "Post offer criminal background check", "outcomesObjectives" : "Ensure study timelines met; Ensure study costs met; Ensure quality metrics met; Ensure compliance protocol; Ensure compliance SOPs; Ensure compliance regulatory requirements; Ensure vendor compliance; Ensure execution project deliverables", "qualificationsBasic" : "Bachelor's degree life sciences, 8 years clinical research, 4 years managing clinical trials, 4-7 years supporting clinical trials, HIPAA/PHI privacy training, Human Subjects Protection training, GCP training", "qualificationsPreferred" : "Advanced degree, Managing CROs experience", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "POSITION SUMMARY: The Manager, Clinical Trials will be responsible for managing all aspects of clinical trials from start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects of the trials independently, and is expected to provide functional expertise to ensure that study timelines, costs and quality metrics are met and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements. PRIMARY RESPONSIBILITIES: Manage the execution and conduct of all aspects of very complex clinical studies to ensure that timelines, cost, and quality metrics are met Responsible for selection of vendors/CROs and provide effective ongoing management to vendors/CROs working on the project to ensure compliance and execution of project deliverables within the approved budget, study timeline, and study protocol. Works closely with investigative site personnel, CROs, and other study vendors Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites Lead study-related activities such as protocol and informed consent preparation, investigator selection, study training material development and delivery, monitoring plans development and execution, CRFs, design and completion, TMF maintenance, protocol amendment and clinical report preparation, as required Collaborate with Clinical Data Management group to ensure correct CRFs content is collected, prepare comprehensive completion guidelines, and design effective data listings and study reports Train CROs, vendors, investigators and study coordinators on implementation of study protocol Hire, train, manage and oversee Clinical trial staff, and serve as a resource for others within the company for clinical trials management expertise Monitor and track clinical trial progress and provide status update to stakeholders Support sample management and prospective sample testing for studies where Natera functions as a central testing facility Partner with other research and development groups to create a culture of mutual respect and focus on delivery of high-quality project results Develop Clinical Department SOPs and participate in audits as needed This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job. Employee must provide records of current training or complete training relating to HIPAA/PHI privacy, Human Subjects Protection, and GCP training. Must maintain a current status on Natera training requirements including General Policies and Procedure Compliance and security training. Employee must pass post offer criminal background check QUALIFICATIONS: Bachelor’s degree in life sciences, or other relevant discipline required, Advanced degree preferred. 8 years of clinical research experience, including at least 4 years of experience in managing clinical trials as a leading role. 4-7 years of experience in supporting clinical trials in a regulated environment . Experience in managing CROs is preferred. KNOWLEDGE, SKILLS, AND ABILITIES: Knowledge and understanding of Clinical Trial SOPs, FDA Regulations, and ICH-GCPs governing the conduct of clinical trials Demonstrated analytical skills and ability to identify problems and solutions independently Ability to collaborate with the study team, cross functional team members and external collaborators Proficiency in MS Word, Excel and PowerPoint Good organization and planning skills Strong interpersonal skills and communication skills (both written and oral) Strong leadership skills, self-motivated, adaptable to a dynamic and fast paced environment Must have excellent organizational and time management skills. Ability to prioritize and handle multiple tasks and projects in a fast-paced environment The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations. Remote USA $115,800—$144,700 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management. WHAT WE OFFER Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program! For more information, visit www.natera.com. Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide. All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws. If you are based in California, we encourage you to read this important information for California residents. Link: https://www.natera.com/notice-of-data-collection-california-residents/ Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes. For more information: - BBB announcement on job scams - FBI Cyber Crime resource page", "summaryDescription" : "Manager, Clinical Trials at Natera. Skills: Clinical trials management, Regulatory requirements, Vendor management. Manage clinical trials execution. Ensure timelines met", "postedDate" : "2026-06-13T22:34:08.935", "createdAt" : "2026-06-13T22:34:08.935", "lastUpdated" : "2026-06-15T07:13:41.897", "ingestTimestamp" : "2026-06-13T22:34:08.935", "mongoId" : "6a2c90ad74d8ee00a0981074", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 110000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Clinical trial execution", "Clinical trial management", "Regulatory compliance", "GCP compliance", "Analytical skills", "Organization skills", "Planning skills", "Time management skills", "Prioritization skills", "Leadership", "Clinical trials management", "Regulatory requirements", "Vendor management", "Functional expertise", "Study contracting", "Budget forecasting", "Accruals payment", "Protocol preparation", "Investigator selection", "Monitoring plans", "CRF completion", "TMF maintenance", "Clinical report preparation", "Data management", "Sample management", "Prospective sample testing", "SOP development", "Audit participation", "Study timelines", "Study costs", "Quality metrics", "Clinical Trial SOPs", "FDA Regulations", "ICH-GCPs", "Clinical trials", "Regulated environment", "PHI privacy", "Human Subjects Protection", "GCP", "Cell-free DNA testing", "Oncology", "Women's health", "Organ health", "Genetic testing", "Genetic diagnostics", "HIPAA/PHI privacy training", "Human Subjects Protection training", "GCP training", "MS Word", "MS Excel", "MS PowerPoint" ], "skillCount" : 51, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Manager", "dataQualityScore" : 0.8888889, "_score" : 960.61224, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a75c174d8ee00a0659266", "title" : "Sr. Cell Therapy Clinical Educator", "company" : "Legend Biotech", "industry" : "biotechnology", "salary" : { "min" : 145000.0, "max" : 210000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Cell Therapy Clinical Educator in the United States, adjusted for industry and company size." }, "location" : "United States", "locations" : [ "United States" ], "certifications" : [ "RN", "NP", "PA" ], "timestamp" : "2026-06-14T07:12:07.243", "fingerprint" : "2d9de2332160a2de85ccbbbe61871d7cf4e6d91625c0ab5244f4ed2376c8a8c1", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/legendcareers/jobs/4703889005", "externalId" : "4703889005", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chicago", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.8755616,-87.6244212" }, { "city" : "Tel Aviv", "country" : "Israel", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "32.0852997,34.7818064" }, { "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "Chicago, Illinois, United States; Tel Aviv, Israel; United States", "minimumEducation" : "Bachelor's Degree", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Microsoft Office, Word, Excel, Outlook, PowerPoint", "professionalSkills" : [ "Clinical developments", "Business acumen", "Organizational goals" ], "hardSkillsList" : [ "Oncology experience" ], "softSkillsList" : [ "Interpersonal skills", "Communication skills", "Presentation skills", "Customer focus" ], "hardSkills" : [ { "name" : "Oncology experience", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Interpersonal skills" }, { "name" : "Communication skills" }, { "name" : "Presentation skills" }, { "name" : "Customer focus" } ], "majorSkills" : "Cell Therapy, Clinical Educator, Oncology", "majorSkillsList" : [ "Cell Therapy", "Clinical Educator", "Oncology" ], "coreResponsibilities" : "Stays current in clinical developments, Develops presentation skills, Facilitate communication of clinical information, Documents all interactions, Documents clinical insights, Documents customer profile information, Attends clinically relevant meetings, Maintains professional standards", "teamCollaboration" : "Internal functional partners; External customers", "domainKnowledge" : "Immune effector cell therapy; Oncology; Multiple Myeloma", "domainList" : [ "immune-effector-cell-therapy", "oncology", "multiple-myeloma" ], "domainSpecificKnowledge" : [ "Immune effector cell therapy", "Oncology", "Multiple Myeloma" ], "toolProficiency" : [ "Microsoft Office" ], "communicationSkills" : "Written communication; Presentation skills", "documentationSkills" : "Clinical documentation", "continuousLearning" : "Professional development", "problemSolvingSkills" : "Identify critical activities; Adjusts priorities; Read situations quickly; Anticipate problems; Adjust for roadblocks", "specialRequirements" : "Travel 75% of the time", "outcomesObjectives" : "Attain organizational objectives; Attain personal objectives", "qualificationsBasic" : "Bachelor’s Degree in health science, 10 years nursing experience, 5 years Oncology experience, Clinical practice experience in immune effector cell therapy, Valid driver’s license", "qualificationsPreferred" : "Advanced degree, Previous in-house industry sales experience, Previous in-house clinical educator experience, Experience with Multiple Myeloma, Involvement/membership in ONS", "workSiteFlexibility" : "Flexible", "rawDescription" : "Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R operating company labeled scientific data; market dynamics and competitive landscape; regulatory and health care compliance guidelines; corporate policies on appropriate business conduct and ethical behavior; relevant SOPs and guidelines. Stays current in clinical developments related to specific disease states. Develops and maintains advanced presentation skills to facilitate effective communication of clinical information. Documents all interactions, clinical insights and customer profile information daily as directed. Attends clinically relevant meetings for personal/professional development. Maintains the highest level of professional standards in all interactions with customers and other business contacts. Requirements Minimum: Bachelor’s Degree from accredited college or university in a health science field (RN, NP, PA, etc). Advanced degree also considered. Minimum of 10 years nursing experience or 5 years Oncology experience. Clinical practice experience in immune effector cell therapy/bone marrow transplant (required if no previous in-house industry experience). Involvement/membership in ONS (Oncology Nursing Society). Previous in-house industry sales or clinical educator experience. Experience with Multiple Myeloma. Exceptional interpersonal, and communication (written and presentation) skills. Demonstrated ability to access and understand challenges and educational needs of stakeholders and accounts within the assigned geography. Proven customer focus. Demonstration of strong in-person and virtual presentation and engagement skills. Superior clinical skills and business acumen with the proven ability to excel in a technically complex and ambiguous environment. Exceptional collaborator who can effectively develop and work with internal functional partners and external customers. Demonstrated ability to identify critical activities and tasks and adjusts priorities to meet organizational goals and objectives. Demonstrated ability to read situations quickly, anticipate and adjust for problems and roadblocks. Valid driver’s license. Agility in multi-tasking. Able to travel 75% of the time. Proven track record of attaining organizational and personal objectives. Ability to perform administrative responsibilities accurately and on time. Proficient in Microsoft Office (Word, Excel, Outlook, PowerPoint). #Li-JK2 #Li-Remote Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech. EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. For information related to our privacy notice, please review: Legend Biotech Privacy Notice.", "summaryDescription" : "Sr. Cell Therapy Clinical Educator at Legend Biotech. Skills: Cell Therapy, Clinical Educator, Oncology. Stays current in clinical developments. Develops presentation skills", "postedDate" : "2026-06-11T19:01:28.179", "createdAt" : "2026-06-11T19:01:28.179", "lastUpdated" : "2026-06-14T07:12:07.243", "ingestTimestamp" : "2026-06-11T19:01:28.179", "mongoId" : "6a2a75c174d8ee00a0659266", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 145000, "salaryAnnualMax" : 210000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Oncology experience", "Interpersonal skills", "Communication skills", "Presentation skills", "Customer focus", "Cell Therapy", "Clinical Educator", "Oncology", "Clinical developments", "Business acumen", "Organizational goals", "Immune effector cell therapy", "Multiple Myeloma", "RN", "NP", "PA", "Microsoft Office" ], "skillCount" : 17, "jobCategory" : "other", "jobSubcategory" : "external-engagement", "dataQualityScore" : 0.8888889, "_score" : 932.2072, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "biotechnology" }, { "id" : "6a2ad31774d8ee00a0714cdd", "title" : "Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy", "company" : "IQVIA Biotech", "industry" : "Biotech", "salary" : { "min" : 68400.0, "max" : 171000.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "Durham, North Carolina, United States of America", "locations" : [ "Durham, North Carolina, United States of America" ], "timestamp" : "2026-06-14T22:48:52.164", "fingerprint" : "236f23734e0dfede0f974ee7841c62c1019be0a9bc6ca01a34368d0efd36b430", "source" : "workday", "language" : "en", "applyUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Durham-North-Carolina-United-States-of-America/Associate-Clinical-Project-Manager--Immuno-Oncology--Cell-and-Gene-Therapy--IQVIA-Biotech_R1540299", "externalId" : "R1540299", "industryFunction" : { }, "locationPoint" : "42.39953,-74.17236", "structuredLocations" : [ { "city" : "Durham", "state" : "North Carolina", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.9966530,-78.9018053" } ], "locationText" : "Durham, North Carolina, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 2, "experienceLevel" : "Associate", "professionalSkills" : [ "Clinical trials", "Scope management", "Forecasting" ], "hardSkillsList" : [ "ICH-GCP compliance" ], "hardSkills" : [ { "name" : "ICH-GCP compliance", "level" : "intermediate" } ], "majorSkills" : "Clinical trial delivery, Cross-functional team coordination, Risk identification, Solution driving", "majorSkillsList" : [ "Clinical trial delivery", "Cross-functional team coordination", "Risk identification", "Solution driving" ], "coreResponsibilities" : "Support delivery of clinical trials, Contribute to study plans, Oversee assigned study components, Coordinate cross-functional teams, Meet timelines and milestones, Monitor study progress, Identify risks, Drive solutions, Ensure compliance with protocols, Ensure compliance with SOPs, Ensure compliance with regulatory requirements, Support project financials, Support forecasting, Support scope management, Communicate updates to internal teams, Communicate updates to clients, Lead sub-teams, Lead vendors", "teamCollaboration" : "Collaborate across teams; Coordinate cross-functional teams; Communicate with internal teams; Communicate with clients; Lead sub-teams; Lead vendors", "projectManagementSkills" : [ "Project leadership", "Study plans", "Study components oversight", "Timeline management", "Milestone management", "Risk monitoring", "Solution driving", "Financial support", "Forecasting support", "Scope management" ], "domainKnowledge" : "Immuno-Oncology; Cell & Gene Therapy; Clinical trial processes; ICH-GCP", "domainList" : [ "immuno-oncology", "cell-gene-therapy", "clinical-trial-processes", "ich-gcp" ], "domainSpecificKnowledge" : [ "Immuno-Oncology", "Cell & Gene Therapy", "Clinical trial processes", "ICH-GCP" ], "toolProficiency" : [ "MS Office tools" ], "communicationSkills" : "Communicate updates", "problemSolvingSkills" : "Problem-solving skills; Identify risks; Drive solutions", "outcomesObjectives" : "Deliver clinical trials; Execute studies on time; Execute studies on budget; Execute studies at highest quality", "qualificationsBasic" : "Bachelor's degree in life sciences, 2+ years clinical research experience, Understanding of clinical trial processes, Understanding of regulatory requirements, Project coordination skills, Organization skills, Problem-solving skills, Excellent communication abilities, Excellent stakeholder management abilities, Manage multiple priorities, Proficiency with MS Office tools", "qualificationsPreferred" : "Cell & Gene Therapy experience, CAR-T experience, Cellular therapies experience, Immunotherapy experience, Global project management experience, Study start-up experience, Study initiation experience, Study close-out experience, First-in-human trials experience, Dose escalation studies experience, Dose expansion studies experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "_IQVIA Biotech is a full-service CRO purpose-built to serve_ _biotech sponsors. With over 25 years of experience, we offer_ _agile, therapeutically aligned solutions and trusted_ _partnerships that help bring breakthrough treatments to_ _patients faster._ As an Associate Project Manager (APM), you’ll play a critical role in delivering clinical trials that bring innovative therapies to patients faster. You’ll support project leadership, collaborate across teams, and help ensure studies are executed on time, on budget, and at the highest quality standards. This role offers strong growth potential, including opportunities to lead smaller studies. **Overview** * Support delivery of clinical trials across Immuno-Oncology and Cell & Gene Therapy programs * Contribute to study plans and oversee assigned study components * Coordinate cross-functional teams to meet timelines and milestones * Monitor study progress, identify risks, and drive solutions * Ensure compliance with protocols, SOPs, and regulatory requirements (ICH-GCP) * Support project financials, forecasting, and scope management * Communicate updates to internal teams and clients * Lead sub-teams or vendors, as needed **Qualifications:** * Bachelor’s degree in life sciences or related field * ~2+ years of clinical research experience * Understanding of clinical trial processes and regulations (ICH-GCP) * Strong project coordination, organization, and problem-solving skills * Excellent communication and stakeholder management abilities * Ability to manage multiple priorities in a fast-paced environment * Proficiency with MS Office tools **Preferred Experience** * Cell & Gene Therapy, including CAR-T and cellular therapies * Immunotherapy * Global project management * Study start-up & initiation and study close-out * First-in-human trials * Dose escalation and dose expansion studies IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at [https://jobs.iqvia.com](https://jobs.iqvia.com/) IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.", "summaryDescription" : "Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy at IQVIA Biotech. Skills: Clinical trial delivery, Cross-functional team coordination, Risk identification, Solution driving. Support delivery of clinical trials. 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: "Regulatory requirements", "level" : "intermediate" }, { "name" : "Staff performance", "level" : "intermediate" }, { "name" : "Protocol compliance", "level" : "intermediate" }, { "name" : "Project status monitoring", "level" : "intermediate" }, { "name" : "Project status analysis", "level" : "intermediate" }, { "name" : "Functional departments coordination", "level" : "intermediate" }, { "name" : "Vendor coordination", "level" : "intermediate" }, { "name" : "Project performance monitoring", "level" : "intermediate" }, { "name" : "Contingency plan development", "level" : "intermediate" }, { "name" : "Task prioritization", "level" : "intermediate" }, { "name" : "Priority setting", "level" : "intermediate" }, { "name" : "Training needs assessment", "level" : "intermediate" }, { "name" : "Training needs coordination", "level" : "intermediate" }, { "name" : "Escalation process management", "level" : "intermediate" }, { "name" : "Quality review findings", "level" : "intermediate" }, { "name" : "Peer feedback analysis", "level" : "intermediate" }, { "name" : "Best practice collaboration", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Clinical trial management, Operational planning, Stakeholder management", "majorSkillsList" : [ "Clinical trial management", "Operational planning", "Stakeholder management" ], "coreResponsibilities" : "Drive successful execution of protocols, Drive successful execution of projects, Support building strategy to deliver trial, Support building strategy to deliver project, Monitor project status, Analyze project status, Ensure successful completion of project parameters, Ensure successful completion of project milestones, Ensure successful completion of project timetables, Proactively manage risks on trials, Proactively manage risks on projects, Implement mitigations, Act as principal liaison between Sponsor, Act as principal liaison between Care Access, Facilitate information flow, Escalate issues, Escalate potential issues, Provide timely project updates, Coordinate cross functional team, Support delivery of clinical trial, Hold teams accountable for delivery, Hold teams accountable for success, Lead teams to successfully deliver, Coordinate activities of functional departments, Coordinate activities of vendors, Develop plans for project implementation, Develop guidelines for project implementation, Identify required data, Identify required analytics, Allow data-driven decisions, Continuously monitor project performance, Evaluate growth opportunities, Develop strategy for initiatives, Identify potential risks, Develop contingency plans, Plan study specific tasks, Communicate study specific tasks, Plan project priorities, Communicate project priorities, Ensure appropriate assessment of training needs, Ensure appropriate coordination of training needs, Maintain project logs, Maintain project trackers, Support essential documentation, Support follow up of monitoring visits, Provide recommendations to challenges, Provide alternative resolutions to challenges, Ensure guidelines are followed, Ensure processes are followed, Escalate out of parameter issues, Escalate identified findings from reviews, Collaborate on best practices, Lead study startup process, Support site evaluation visits, Support site selection visits, Have sites selected, Have sites successfully activated, Review study information, Liaise with key stakeholders, Communicate study needs, Communicate site needs, Communicate performance expectations, Establish timelines, Help address questions onsite, Assess risks onsite, Mitigate issues onsite, Initiate study related processes, Partner with client to drive startup, Drive startup activities, Drive startup timelines, Drive expectations of startup process, Ensure information transition to sites, Assess study start up processes, Optimize study start up processes, Enhance efficiency, Enhance productivity, Monitor key performance indicators, Track progress, Identify areas of improvement, Be main point of contact with sponsor, Drive study activation", "teamCollaboration" : "Cross functional team; Global organization stakeholders; Fellow CTMs; Department leadership; Client communication", "projectManagementSkills" : [ "Project execution", "Timeline management", "Budget management", "Quality standards", "Risk management", "Mitigation implementation", "Project updates", "Project planning", "Project implementation", "Project performance", "Contingency planning", "Task prioritization", "Priority setting", "Study startup", "Startup activities", "Startup timelines" ], "domainKnowledge" : "Clinical trial protocols; Regulatory requirements; Decentralized trial model; Therapeutic areas", "domainList" : [ "clinical-trial-protocols", "regulatory-requirements", "decentralized-trial-model", "therapeutic-areas" ], "domainSpecificKnowledge" : [ "Clinical trial protocols", "Regulatory requirements", "Decentralized trial model", "Therapeutic areas" ], "toolProficiency" : [ "Care Access tools" ], "communicationSkills" : "Information flow; Project updates; Interpersonal communication; Written communication; Verbal communication", "documentationSkills" : "Essential documentation; Project logs; Project trackers", "problemSolvingSkills" : "Problem-solving; Risk management; Mitigation; Issue escalation; Alternative resolutions; Challenge resolution", "specialRequirements" : "Less than 25% travel, Occasional planned travel, Use keyboards, Use computer equipment", "outcomesObjectives" : "Successful execution of protocols; Successful execution of projects; Successful completion of project parameters; Successful completion of project milestones; Successful completion of project timetables; Successful delivery in areas; Successful site activation", "qualificationsBasic" : "Exceptional strategic thinking, Problem-solving skills, Effective leadership skills, Communication competency, Ability to foster team productivity, Ability to foster team cohesiveness, Ability to show flexibility, Ability to pivot workflows, Ability to adjust priorities, Ability to work independently, Organize work with attention to detail, Demonstrated skill in assessing timelines, Coordinating numerous assignments, Coordinating numerous projects simultaneously, High degree of discretion, Ability to work flexible hours, Ability to mentor junior team members, Excellent written communication skills, Excellent verbal communication skills, Excellent interpersonal communication skills, Comfortable in a fast-paced environment, Experience anticipating problems, Experience resolving problems on projects, Experience reporting project details", "qualificationsPreferred" : "Experience with decentralized trial model", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About Care Access Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow. With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all. To learn more about Care Access, visit www.CareAccess.com. How This Role Makes a Difference The Clinical Trial Manager is a central leadership role within all (study) operations. The CTM is responsible to drive the successful execution of protocols or projects, including within the decentralized trial model when applicable, from strategic planning through close out within agreed upon timelines, budget, alignment with all applicable SOPs and regulatory requirements. The CTM would serve as a key operational component at the site and play a role in staff performance, protocol compliance, and long-term quality planning. How You'll Make An Impact Drives and Manages studies or projects according to scope of work, timelines, and quality standards. Supports building a strategy to deliver the trial or project as per protocol and timelines. Monitors and analyses project status to ensure successful completion of project parameters, milestones, timetables. Understands proactively manages risks on trials or projects and implements mitigations whilst working in a cross functional team. Acts as principal liaison between Sponsor and Care Access by facilitating the flow of information between Care Access and client. Appropriately escalates any issues or potential issues as per escalation pathways; and provides timely project updates to upline management and/or Senior Leadership at Care Access. Coordinates a cross functional team to support delivery of the clinical trial. Holds teams accountable for delivery and success of the trial. Leads teams to successfully deliver in their areas. Coordinates activities of all functional departments and vendors involved in the project. Works with team and management to develop plans/guidelines for project implementation using Care Access tools.  Identifies data and analytics required to allows data-driven decisions and continuously monitors ongoing project performance. Evaluates growth opportunities of current engagement or potential engagements; helps develops the strategy for various initiatives. Works with team to identify potential risks, develop contingency plans. Plans and communicates to team members to study specific tasks and priorities for projects.  Ensures that appropriate assessment and coordination of project/protocol specific and therapeutic area training needs and activities are occurring for the team members as needed. Maintains project logs and trackers. Supports essential documentation and follow up of monitoring visits Provides recommendations and alternative resolutions to project-specific challenges through established escalation channels. Ensures guidelines and processes are followed for efficient escalation of out of parameter issues as appropriate. Escalates identified findings from periodic quality reviews and peer feedback reports. Collaborates with fellow CTMs and department leadership on best practices. Study Start Up: Lead the process of study startup to support site evaluation/selection visits on each new study and help to have sites selected and successfully activated, based off of study requirements Review study information and liaise with key stakeholders across the global organization to communicate study/site needs, requirements, performance expectations and establish timelines Work closely with the staff onsite to help address questions, assess risks and mitigate issues throughout startup Partner with other Care Access teams to initiate study related processes at the appropriate SSU milestone (e. g. capacity planning, systems build requests, etc.) Partner and communicate with client to drive startup activities, timelines, and expectations of Care Access startup process Ensure that all information gained during the startup process is completely transitioned to sites, as required Continue to assess and optimize study start up processes to enhance efficiency and productivity Monitor key performance indicators to track progress and identify areas of improvement Be main point of contact with the sponsor to drive study activation The Expertise Required Exceptional strategic thinking and problem-solving skills to drive Care Access goals while fostering and maintaining a strong client relationship. Effective leadership skills, strong communication competency, and proven ability to foster team productivity and cohesiveness. Ability to show flexibility by pivoting workflows and adjusting priorities as needed. Ability to work independently, organize work with attention to detail ‎and accuracy; demonstrated skill in assessing timelines and coordinating numerous ‎assignments and projects simultaneously under heavy and fluctuating workloads and ‎conflicting deadlines. High degree of discretion in dealing with confidential information. Ability and willingness to work flexible hours when needed. Ability to mentor junior team members. Excellent written, verbal, and interpersonal communication skills. Comfortable in a fast-paced environment. Certifications/Licenses, Education, and Experience Must have clinical trial experience. Decentralized clinical trial experience, preferred. Site experience, preferably in a site network. PMP Certification, preferred. Bachelor's degree Must have 6+ years of experience in the clinical trial/pharmaceutical industry. Must have 4+ years in project management including client management. Must have 1-2 years strategy consulting experience. Experience with oversight of external vendors (e.g., e-consent vendor). Experience collaborating and leading cross-functional teams in a matrix environment. Experience managing multiple projects across various therapeutic areas. Experience anticipating and resolving problems on projects. Experience reporting project details to various stakeholders within the company and outside of the company How We Work Together Location: Remote within Canada. This role requires 100% of work to be performed in a remote office environment. Travel: This is a remote position with less than 25% national travel requirements. Occasional planned travel may be required as part of the role. Physical demands associated with this position Include: The ability to use keyboards and other computer equipment. Benefits & Perks Paid Time Off (PTO) and Company Paid Holidays Medical, dental, and vision insurance plan options Diversity & Inclusion We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Care Access is unable to sponsor work visas at this time. If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com Mandatory Employer Disclosures: Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment. Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment. Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws. Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.", "summaryDescription" : "Clinical Trial Manager at Care Access. Skills: Clinical trial management, Operational planning, Stakeholder management. Drive successful execution of protocols. Drive successful execution of projects", "postedDate" : "2026-06-11T19:09:32.785", "createdAt" : "2026-06-11T19:09:32.785", "lastUpdated" : "2026-06-14T09:25:43.780", "ingestTimestamp" : "2026-06-11T19:09:32.785", "mongoId" : "6a2a5cee74d8ee00a06172dc", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Regulatory requirements", "Staff performance", "Protocol compliance", "Project status monitoring", "Project status analysis", "Functional departments coordination", "Vendor coordination", "Project performance monitoring", "Contingency plan development", "Task prioritization", "Priority setting", "Training needs assessment", "Training needs coordination", "Escalation process management", "Quality review findings", "Peer feedback analysis", "Best practice collaboration", "Leadership", "Mentoring", "Clinical trial management", "Operational planning", "Stakeholder management", "Protocol execution", "Quality planning", "Risk management", "Data-driven decisions", "Project implementation", "Study startup", "Site evaluation", "Site selection", "Capacity planning", "Systems build", "Project execution", "Timeline management", "Budget management", "Quality standards", "Mitigation implementation", "Project updates", "Project planning", "Project performance", "Contingency planning", "Startup activities", "Startup timelines", "Clinical trial protocols", "Decentralized trial model", "Therapeutic areas", "Care Access tools" ], "skillCount" : 47, "jobCategory" : "other", "jobSubcategory" : "trial-management", "dataQualityScore" : 0.8888889, "_score" : 897.8949, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a2ac2eb74d8ee00a06f8464", "title" : "Clinical Trial Manager", "company" : "Generate Biomedicines", "salary" : { "min" : 127000.0, "max" : 170000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Somerville, Massachusetts, United States", "locations" : [ "Somerville", "Massachusetts", "United States" ], "timestamp" : "2026-06-14T22:50:06.003", "fingerprint" : "2c432bdc29328fc5cd16732f8ea588fbd0fa14aa64286f6ada094388be53114c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://generatebiomedicines.com/open-positions?gh_jid=4683639006", "externalId" : "4683639006", "structuredLocations" : [ { "city" : "Somerville", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3875968,-71.0994968" } ], "locationText" : "Somerville, Massachusetts, United States", "experienceLevel" : "Manager", "technicalSkills" : "CTMS, EDC, eTMF", "professionalSkills" : [ "Clinical operations", "Clinical research", "Vendor management", "Study startup", "Data reviews", "Invoice review", "Budget tracking", "Data reconciliation" ], "hardSkillsList" : [ "TMF completeness", "IRB/IEC tracking", "SAE/SUSAR notifications", "Protocol deviations" ], "softSkillsList" : [ "Organized", "Clear communicator", "Attention to detail" ], "hardSkills" : [ { "name" : "TMF completeness", "level" : "intermediate" }, { "name" : "IRB/IEC tracking", "level" : "intermediate" }, { "name" : "SAE/SUSAR notifications", "level" : "intermediate" }, { "name" : "Protocol deviations", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Organized" }, { "name" : "Clear communicator" }, { "name" : "Attention to detail" } ], "majorSkills" : "Clinical trial management, CRO coordination, Vendor oversight", "majorSkillsList" : [ "Clinical trial management", "CRO coordination", "Vendor oversight" ], "coreResponsibilities" : "Serve as operational point of contact for CROs, Serve as operational point of contact for vendors, Track study deliverables, Track study timelines, Flag risks or delays to leadership, Review CRO-generated study documents, Support coordination of study startup activities, Maintain and update study trackers, Maintain and update study timelines, Maintain and update action items, Attend cross-functional study team meetings, Support cross-functional study team meetings, Document meeting minutes, Track action items, Follow up on outstanding deliverables, Track protocol deviations, Triage protocol deviations, Coordinate with vendors on deviations, Coordinate with internal teams on deviations, Ensure timely documentation of deviations, Ensure timely resolution of deviations, Support safety reporting coordination, Track SAE/SUSAR notifications, Ensure timely distribution of notifications, Monitor TMF completeness, Support inspection readiness activities, Resolve TMF filing gaps, Maintain TMF document quality, Assist with IRB/IEC tracking, Compile enrollment metrics, Compile site performance metrics, Compile operational metrics, Distribute enrollment metrics, Distribute site performance metrics, Distribute operational metrics, Contribute to data reviews, Track data cleaning progress, Review monitoring visits, Review monitoring visit reports, Ensure high quality monitoring, Ensure adherence to monitoring plan, Support vendor invoice review, Support budget tracking, Reconcile CRO invoices, Flag invoice discrepancies, Coordinate data reconciliation activities, Support onboarding of CTAs, Serve as resource for study questions", "teamCollaboration" : "Cross-functional teams; Clinical operations leadership; Data management", "projectManagementSkills" : [ "Timeline management", "Action item tracking" ], "domainKnowledge" : "Clinical trial processes; Oncology; Immunology; Respiratory", "domainList" : [ "clinical-trial-processes", "oncology", "immunology", "respiratory" ], "domainSpecificKnowledge" : [ "Clinical trial processes", "Oncology", "Immunology", "Respiratory" ], "toolProficiency" : [ "CTMS platforms", "EDC platforms", "eTMF platforms" ], "communicationSkills" : "Escalate issues", "documentationSkills" : "Study documents; TMF entries; Regulatory documents; Meeting minutes", "specialRequirements" : "Travel up to 20%", "qualificationsBasic" : "6+ years of experience in clinical operations, Foundational understanding of GCP, Foundational understanding of ICH guidelines, Foundational understanding of clinical trial processes, Experience working with or alongside CROs, Experience working with or alongside clinical vendors, Ability to manage multiple trackers, Ability to manage multiple timelines, Ability to manage multiple action items", "qualificationsPreferred" : "Bachelor’s degree scientific preferred, Bachelor’s degree health-related field preferred, Clinical research sponsor-side experience, Familiarity with oncology therapeutic areas, Familiarity with immunology therapeutic areas, Familiarity with respiratory therapeutic areas", "rawDescription" : "The Role: Generate Biomedicines is seeking an organized and proactive Clinical Trial Manager (CTM) to support the operational execution of late-stage clinical trials within our Clinical Development team. This role will report to the Director, Clinical Operations and will serve as a key day-to-day operational coordinator across assigned studies. At Generate Biomedicines, clinical execution is carried out through a network of CROs and specialized vendors. The CTM plays a critical role in ensuring that these external partners stay on track monitoring deliverables, flagging issues, coordinating internally, and escalating to clinical operations leadership when needed. This is an excellent opportunity for a detail-driven professional looking to grow their clinical operations career on the sponsor side Here's how you will contribute: Serve as a day-to-day operational point of contact for assigned CROs and vendors, tracking study deliverables and timelines and flagging risks or delays to clinical operations leadership. Review CRO-generated study documents for completeness and quality, including monitoring visit reports, site correspondence, protocol deviations, and TMF entries. Support the coordination of study startup activities, including site activation tracking, regulatory document collection, and vendor kick-off preparation. Maintain and update study trackers, timelines, and action logs; ensure cross-functional teams have visibility into study status and open items. Attend and support cross-functional study team meetings; document meeting minutes, track action items, and follow up on outstanding deliverables. Track and triage protocol deviations reported by CROs; coordinate with vendors and internal teams to ensure timely documentation and resolution. Support safety reporting coordination, including tracking SAE/SUSAR notifications and ensuring timely distribution to sites and relevant stakeholders in line with vendor responsibilities. Monitor TMF completeness and support inspection readiness activities, working with CROs to resolve filing gaps and maintain document quality standards. Assist with IRB/IEC tracking across study sites, including monitoring approval status for amendments and annual renewals submitted by the CRO. Compile and distribute enrollment, site performance, and operational metrics to clinical operations leadership on a regular basis. Contribute to data reviews as needed, and track data cleaning progress performed by CRO. Review and track monitoring visits and monitoring visit reports performed by CRO to ensure high quality and adherence to the monitoring plan. Support vendor invoice review and budget tracking by reconciling CRO invoices against contracted activities and flagging discrepancies. Coordinate data reconciliation activities at key study milestones in collaboration with data management and the CRO. Support the onboarding of CTAs joining the study team and serve as a resource for day-to-day study questions. The Ideal Candidate will have: Bachelor’s degree required; scientific or health-related field preferred. 6+ years of experience in clinical operations, clinical research, or a related field; sponsor-side experience is a plus. Foundational understanding of GCP, ICH guidelines, and clinical trial processes. Experience working with or alongside CROs or clinical vendors in a coordination or support capacity. Strong attention to detail and ability to manage multiple trackers, timelines, and action items simultaneously. Comfortable working in a structured, vendor-managed model where the role is one of oversight and coordination rather than direct execution. Familiarity with clinical trial systems such as CTMS, EDC, and eTMF platforms. Clear communicator with the ability to follow up consistently and escalate issues in a timely manner. Familiarity with therapeutic areas such as oncology, immunology, and/or respiratory is a plus. Ability to travel up to 20% of the time, domestically and/or internationally, as study needs require. About Generate Biomedicines We are a clinical-stage generative biology company pioneering the AI revolution in drug design and development. We are advancing a new approach to drug creation—one grounded in the ability to design proteins with defined biological intent. By integrating machine learning with large-scale experimentation, this approach aims to reduce the uncertainty, time, and cost associated with developing protein-based medicines. Founded in 2018, we are advancing a growing pipeline of clinical and preclinical programs across multiple disease areas and protein modalities. By unifying computational design and clinical development within a single operating model, we translate this approach into clinical-stage programs and are leading a shift from traditional drug discovery toward systematic drug generation. At Generate:Biomedicines, we collaborate across disciplines in new ways to invent and innovate. We bring diverse perspectives to a shared goal of delivering better medicines to patients in need, faster, guided by our values and leadership behaviors. Generate:Biomedicines is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Recruitment & Staffing Agencies: Generate:Biomedicines does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Generate:Biomedicines or its employees is strictly prohibited unless contacted directly by the Company’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Generate:Biomedicines and the Company will not owe any referral or other fees with respect thereto. LI-RT1 Compensation: The base salary range provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package. Per Year Salary Range $127,000—$170,000 USD", "summaryDescription" : "Clinical Trial Manager at Generate Biomedicines. Skills: Clinical trial management, CRO coordination, Vendor oversight. Serve as operational point of contact for CROs. Serve as operational point of contact for vendors", "postedDate" : "2026-06-12T01:38:03.003", "createdAt" : "2026-06-12T01:38:03.003", "lastUpdated" : "2026-06-14T22:50:06.003", "ingestTimestamp" : "2026-06-12T01:38:03.003", "mongoId" : "6a2ac2eb74d8ee00a06f8464", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 127000, "salaryAnnualMax" : 170000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "TMF completeness", "IRB/IEC tracking", "SAE/SUSAR notifications", "Protocol deviations", "Organized", "Clear communicator", "Attention to detail", "Clinical trial management", "CRO coordination", "Vendor oversight", "Clinical operations", "Clinical research", "Vendor management", "Study startup", "Data reviews", "Invoice review", "Budget tracking", "Data reconciliation", "Timeline management", "Action item tracking", "Clinical trial processes", "Oncology", "Immunology", "Respiratory", "CTMS platforms", "EDC platforms", "eTMF platforms" ], "skillCount" : 27, "jobCategory" : "engineering", "jobSubcategory" : "clinical-development", "dataQualityScore" : 0.8888889, "_score" : 890.068, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2cb20e74d8ee00a09df760", "title" : "Principal, Global Feasibility (pre-award strategy)", "industry" : "Analyst", "salary" : { "min" : 175000.0, "max" : 250000.0, "currency" : "CHF", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Principal in Biotech in Switzerland, adjusted for seniority and industry." }, "location" : "Switzerland", "locations" : [ "Switzerland" ], "timestamp" : "2026-06-16T02:53:52.346", "fingerprint" : "0ee6d40b089d1144b832ce26f4d28bae472105f1221526bd43a982f2bf52ab57", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/e178e4e2-0503-4ed4-af15-a2f43dbd7e80/apply", "externalId" : "e178e4e2-0503-4ed4-af15-a2f43dbd7e80", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Switzerland", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "Switzerland", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 3, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Feasibility strategy", "Pre-award strategy", "RFP analysis", "Partnership feasibility", "Site-level feasibility", "Strategic thinking", "Problem-solving", "Data analysis", "Bid defense preparation", "Data management", "Process improvement", "Methodology development" ], "hardSkillsList" : [ "Scientific literature research", "External source research", "Evidence-based decision making", "Documentation maintenance", "Feasibility metrics development", "Framework development" ], "softSkillsList" : [ "Autonomy", "Leadership" ], "hardSkills" : [ { "name" : "Scientific literature research", "level" : "intermediate" }, { "name" : "External source research", "level" : "intermediate" }, { "name" : "Evidence-based decision making", "level" : "intermediate" }, { "name" : "Documentation maintenance", "level" : "intermediate" }, { "name" : "Feasibility metrics development", "level" : "intermediate" }, { "name" : "Framework development", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Autonomy" }, { "name" : "Leadership" } ], "majorSkills" : "Global feasibility, Pre-award strategy, Clinical trial execution", "majorSkillsList" : [ "Global feasibility", "Pre-award strategy", "Clinical trial execution" ], "coreResponsibilities" : "Lead feasibility assessments, Deliver feasibility assessments, Lead pre-award strategy assessments, Deliver pre-award strategy assessments, Develop site-level feasibility outputs, Analyze site-level feasibility outputs, Present site-level feasibility outputs, Design feasibility strategies, Identify innovative solutions, Propose innovative solutions, Conduct advanced research, Support bid defense preparation, Participate in client-facing meetings, Maintain accurate documentation, Ensure high-quality data management, Contribute to departmental metrics development, Contribute to feasibility frameworks development, Contribute to process improvements, Mentor junior team members, Support junior team members, Mentor mid-level team members, Support mid-level team members, Provide guidance on analysis, Provide guidance on reporting, Provide guidance on best practices, Participate in strategic initiatives, Participate in system development, Participate in data asset evaluation, Participate in methodology improvement", "teamCollaboration" : "Cross-functional teams; Global teams", "projectManagementSkills" : [ "Workload management" ], "domainKnowledge" : "Life Sciences; Clinical research; Global clinical feasibility; Country and site selection; Drug development lifecycle; Therapeutic areas", "domainList" : [ "life-sciences", "clinical-research", "global-clinical-feasibility", "country-and-site-selection", "drug-development-lifecycle", "therapeutic-areas" ], "domainSpecificKnowledge" : [ "Life Sciences", "Clinical research", "Global clinical feasibility", "Country and site selection", "Drug development lifecycle", "Therapeutic areas" ], "communicationSkills" : "Written communication; Verbal communication; Presentation abilities; Senior stakeholder engagement", "documentationSkills" : "Accurate documentation", "continuousLearning" : "Training; Professional development support", "innovationCreativity" : "Innovative solutions", "problemSolvingSkills" : "Analytical thinking; Strategic thinking; Problem-solving skills", "qualificationsBasic" : "7+ years experience (BS/RN/MS), 3+ years experience (PhD/MD), Clinical research background, GCP understanding, Study start-up processes, Global clinical feasibility knowledge, Country and site selection knowledge, Drug development lifecycle knowledge, Manage complex workloads, Manage multi-study workloads, Work under tight deadlines, High attention to detail, Synthesize complex data sets, Influence effectively, Negotiate effectively, Work effectively in global teams, Customer-facing roles experience, Consultancy-style roles experience, Manage competing priorities, Fast-paced environment experience", "qualificationsPreferred" : "Advanced degree in Life Sciences", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "## Accountabilities Lead and independently deliver highly complex global feasibility and pre-award strategy assessments across all therapeutic areas, including RFP and partnership feasibility work. Develop, analyze, and present site-level feasibility outputs in both written and presentation formats for internal and external stakeholders. Collaborate cross-functionally with business development, medical directors, business analysts, and operational teams to design optimal feasibility strategies. Identify and propose innovative solutions for non-standard or complex feasibility requests with minimal supervision. Conduct advanced research using scientific literature, internal data systems, and external sources to support evidence-based feasibility decisions. Support bid defense preparation and participate in client-facing meetings with a high level of professionalism and autonomy. Maintain accurate documentation and ensure high-quality data management within internal systems and knowledge repositories. Contribute to the development of departmental metrics, feasibility frameworks, and process improvements to enhance operational efficiency. Mentor and support junior and mid-level team members, providing guidance on analysis, reporting, and best practices. Participate in strategic initiatives, including system development, data asset evaluation, and continuous improvement of feasibility methodologies. Requirements Advanced degree in Life Sciences or related field (BS/RN/MS with 7+ years of experience, or PhD/MD with 3+ years of relevant experience). Strong background in clinical research, including clinical trial execution, GCP understanding, and study start-up processes. Deep knowledge of global clinical feasibility, country and site selection, and drug development lifecycle. Proven ability to independently manage complex, multi-study workloads under tight deadlines while maintaining high attention to detail. Strong analytical, strategic thinking, and problem-solving skills with the ability to synthesize complex data sets into clear insights. Excellent communication skills, including written, verbal, and presentation abilities for senior stakeholder engagement. Demonstrated ability to influence, negotiate, and work effectively in cross-functional, global teams. Experience in customer-facing or consultancy-style roles within clinical research or life sciences environments. Ability to mentor and support junior colleagues while contributing to team capability development. Strong organizational skills with the ability to manage competing priorities in a fast-paced environment. Benefits Competitive compensation and comprehensive global benefits package. Opportunity to work on high-impact, global clinical research programs across multiple therapeutic areas. Strong career development and advancement opportunities within a leading life sciences environment. Exposure to cutting-edge clinical development strategies and global feasibility operations. Collaborative, international, and science-driven work culture. Flexible working arrangements supporting work-life balance. Continuous learning opportunities, including training and professional development support. Participation in high-visibility projects influencing global drug development success. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Principal, Global Feasibility (pre-award strategy). Skills: Global feasibility, Pre-award strategy, Clinical trial execution. Lead feasibility assessments. Deliver feasibility assessments", "postedDate" : "2026-06-12T12:29:19.667", "createdAt" : "2026-06-12T12:29:19.667", "lastUpdated" : "2026-06-16T02:53:52.346", "ingestTimestamp" : "2026-06-14T21:26:21.843", "mongoId" : "6a2cb20e74d8ee00a09df760", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "150k-200k", "hasSalary" : false, "allSkills" : [ "Scientific literature research", "External source research", "Evidence-based decision making", "Documentation maintenance", "Feasibility metrics development", "Framework development", "Autonomy", "Leadership", "Global feasibility", "Pre-award strategy", "Clinical trial execution", "Feasibility strategy", "RFP analysis", "Partnership feasibility", "Site-level feasibility", "Strategic thinking", "Problem-solving", "Data analysis", "Bid defense preparation", "Data management", "Process improvement", "Methodology development", "Workload management", "Life Sciences", "Clinical research", "Global clinical feasibility", "Country and site selection", "Drug development lifecycle", "Therapeutic areas" ], "skillCount" : 29, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "_score" : 868.3452, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c9f2374d8ee00a099f5d4", "title" : "Clinical Trial Management Associate (CTMA), Oncology (EMEA/LATAM)", "company" : "Maleda Tech", "industry" : "Pharma", "salary" : { "min" : 75000.0, "max" : 110000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Trial Management Associate in the United States, adjusted for the biotech industry and remote work." }, "location" : "United States", "locations" : [ "United States" ], "timestamp" : "2026-06-16T03:38:06.688", "fingerprint" : "bbf1458e7c9dedefe71b8bca440e915b1f4614ce3559991846f4e18baa28c92d", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://maleda-tech.breezy.hr/p/be5db92a4dc0-clinical-trial-management-associate-ctma-oncology-emea-latam", "externalId" : "be5db92a4dc0", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "CONTRACT", "professionalSkills" : [ "Clinical operations" ], "majorSkills" : "Clinical trial management", "majorSkillsList" : [ "Clinical trial management" ], "coreResponsibilities" : "Oversee oncology clinical trials, Execute oncology clinical trials", "domainKnowledge" : "Oncology clinical trials; EMEA; LATAM", "domainList" : [ "oncology-clinical-trials", "emea", "latam" ], "domainSpecificKnowledge" : [ "Oncology clinical trials", "EMEA", "LATAM" ], "remoteFriendly" : true, "rawDescription" : "About the Role Maleda is hiring a Clinical Trial Management Associate (CTMA) to serve as a critical clinical operations partner in the execution and oversight of Phase I to III global oncology clinical trials across the EMEA and LATAM regions. Positioned between the Clinical Trial Associate (CTA) a", "summaryDescription" : "Clinical Trial Management Associate (CTMA), Oncology (EMEA/LATAM) at Maleda Tech. Skills: Clinical trial management. Oversee oncology clinical trials. 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Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. We are looking for a Research Associate II to join Dr. Elizabeth Budde's T Cell Therapeutics Research Laboratories. This role involves fast-paced research in cutting-edge technology, immunotherapeutic programs, and a commitment to delivering innovative solutions to critical illnesses. For more information on T Cell Therapeutics research, please visit here . As a successful candidate, you will: · Conduct tissue culture, maintaining cell cultures and applying aseptic techniques for various cell lines, especially T cell lines. · Perform T cell functional assays, including cytotoxicity, cytokine production assays, and ELISAs. · Conduct cell staining for Multicolor Flow Cytometry and analyze flow cytometry data. · Assist in murine surgical procedures, tissue harvesting/preparation, and contribute to revising/maintaining lab protocols. · Provide routine lab support and maintain activities in accordance with Good Laboratory Practices (GLP). Your qualifications should include: · Bachelor’s degree in Biological Sciences or related field, with 2 years of post-degree research experience, or 1 year with a Master’s degree · Exceptional attention to detail, accuracy in lab work, and robust record-keeping skills · Preferred: Master’s degree and hands-on experience in cellular immunology and GLP City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . 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Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. A Quality Assurance Associate III is available in the Beckman Research Institute of City of Hope. You will be responsible for assisting QA Management in achieving compliance with all Federal and State laws and regulations and other accrediting agency requirements in the collection, processing, preparation, and distribution of biopharmaceutical products manufactured in the GMP facilities at City of Hope (COH). As a successful candidate, you will: · Perform quality assurance activities in the QA Compliance function and ensure compliance with Good Manufacturing Practices (GMP). · Administer the Deviation, CAPA, and Change Control programs as Business Process Owner. · Author Deviations in collaboration with originating departments and SMEs. · Track, Trend, and monitor the progress of Deviation, CAPA, and Change Controls in alignment with SOP criteria, assigned due dates, and business timelines. · Provide and evaluate Quality System KPI data in support of Quality Management Review · Schedule and coordinate the Change Control Committee meetings · Conduct internal cGMP training. Maintain training records and the training program. · Coordinate and conduct Internal audits, follow up and write reports for submission to QA management. Track and follow up on audit commitments for timely completion and closure. · Coordinate and conduct Supplier Quality Assessments and maintain the Approved Supplier List. Perform Supplier requalification in alignment with SOP criteria. · Write reviews and process Standard Operating Procedures. Your qualifications should include: · Bachelor’s degree with 6-8 years of experience within Quality Assurance required. · Masters degree preferred with 6+ years of experience or PhD with 1+ years of experience or Bachelors degree with 10+ years of experience preferred. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "QA Associate III - Cell Therapy Manufacturing at City of Hope. Assist QA Management. Achieve compliance", "createdAt" : "2026-06-14T07:29:59.135", "lastUpdated" : "2026-06-15T09:15:11.038", "ingestTimestamp" : "2026-06-14T07:29:59.135", "mongoId" : "69dde45c2beec4dd3d9a3f4b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 135000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Good Manufacturing Practices", "Biopharmaceutical products", "GMP facilities" ], "skillCount" : 3, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Senior", "dataQualityScore" : 0.7777778, "_score" : 855.6096, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c5e6674d8ee00a08e3c3b", "title" : "Senior Clinical Trial Manager (Lupus)", "company" : "Beeline Medicines", "industry" : "Biotechnology", "salary" : { "min" : 155000.0, "max" : 215000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for Senior Clinical Trial Manager in the United States, adjusted for seniority and the biotech industry." }, "location" : "United States", "locations" : [ "United States" ], "timestamp" : "2026-06-15T00:48:39.589", "fingerprint" : "ae98973d1ba25e60a069a721aa12cdfae32f97255a9688e2bd82da99bbb9ce56", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/beelinemedicines/jobs/4247380009", "externalId" : "4247380009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chicago", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.8755616,-87.6244212" }, { "city" : "Tel Aviv", "country" : "Israel", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "32.0852997,34.7818064" }, { "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "Chicago, Illinois, United States; Tel Aviv, Israel; United States", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Clinical trial management", "Regulatory compliance", "Vendor management", "Budget development", "Protocol development", "Risk mitigation", "Data collection", "Inspection readiness", "Audit preparation" ], "hardSkillsList" : [ "Clinical operations", "Global clinical trials", "Immunology indications", "Autoimmune diseases", "Inflammatory diseases", "Monoclonal antibodies", "Advanced therapies", "Clinical trial regulations", "Operational best practices", "Pivotal trials" ], "softSkillsList" : [ "Leadership", "Problem-solving" ], "hardSkills" : [ { "name" : "Clinical operations", "level" : "intermediate" }, { "name" : "Global clinical trials", "level" : "intermediate" }, { "name" : "Immunology indications", "level" : "intermediate" }, { "name" : "Autoimmune diseases", "level" : "intermediate" }, { "name" : "Inflammatory diseases", "level" : "intermediate" }, { "name" : "Monoclonal antibodies", "level" : "intermediate" }, { "name" : "Advanced therapies", "level" : "intermediate" }, { "name" : "Clinical trial regulations", "level" : "intermediate" }, { "name" : "Operational best practices", "level" : "intermediate" }, { "name" : "Pivotal trials", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Problem-solving" } ], "majorSkills" : "Clinical trial operations, Global study execution, Immunology trials", "majorSkillsList" : [ "Clinical trial operations", "Global study execution", "Immunology trials" ], "coreResponsibilities" : "Lead operational strategy, Plan clinical trials, Execute clinical trials, Oversee clinical trials, Serve as primary operational point of contact, Oversee selection of CROs, Oversee management of vendors, Drive site feasibility, Drive site selection, Drive site activation, Drive patient recruitment strategies, Manage ongoing site management, Develop study timelines, Maintain study timelines, Develop risk mitigation strategies, Maintain risk mitigation strategies, Develop operational tracking tools, Maintain operational tracking tools, Collaborate on protocol development, Collaborate on CRF design, Collaborate on ICF review, Collaborate on operational study plans, Ensure studies are conducted in compliance, Identify operational issues, Resolve operational issues, Escalate risks, Implement mitigation strategies, Oversee data collection activities, Oversee database lock readiness, Support data review processes, Contribute to regulatory filings, Contribute to inspection readiness, Contribute to audit preparation, Provide leadership to Clinical Operations team, Provide mentorship to Clinical Operations team, Contribute to process improvement initiatives", "teamCollaboration" : "Internal cross-functional teams; External partners; CROs and vendors; Clinical Operations team members", "projectManagementSkills" : [ "Study timelines", "Risk mitigation", "Operational tracking" ], "domainKnowledge" : "Immunology; Autoimmune diseases; Inflammatory diseases; Biologics; Monoclonal antibodies; Advanced therapies; GCP/ICH guidelines; Clinical trial regulations", "domainList" : [ "immunology", "autoimmune-diseases", "inflammatory-diseases", "biologics", "monoclonal-antibodies", "advanced-therapies", "gcp-ich-guidelines", "clinical-trial-regulations" ], "domainSpecificKnowledge" : [ "Immunology", "Autoimmune diseases", "Inflammatory diseases", "Biologics", "Monoclonal antibodies", "Advanced therapies", "GCP/ICH guidelines", "Clinical trial regulations" ], "toolProficiency" : [ "CTMS", "EDC", "eTMF", "Risk-based monitoring tools" ], "documentationSkills" : "CRF design; ICF review; Operational study plans; Regulatory filings", "problemSolvingSkills" : "Problem-solving; Risk mitigation; Issue resolution", "specialRequirements" : "Periodic travel to Beeline Medicines offices, Domestic and international travel up to 20%", "outcomesObjectives" : "Ensure studies delivered on time; Ensure studies within scope; Ensure compliance with regulatory standards; Achieve enrollment goals", "qualificationsBasic" : "Bachelor’s degree in life sciences, Minimum 5 years of experience in clinical operations, At least 3 years in a Senior CTM role, Proven track record of managing global clinical trials, Experience with biologics, Knowledge of GCP/ICH guidelines, Availability during Eastern Time (ET) business hours", "qualificationsPreferred" : "Advanced degree preferred, Experience in rare autoimmune indications, Familiarity with adaptive trial designs, Experience in early- to late-stage development programs", "workSiteFlexibility" : "Hybrid", "rawDescription" : "About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully. Job Summary: The Senior Clinical Trial Manager (Sr. CTM) will lead the operational planning, execution, and oversight of complex, global clinical studies in the field of immunology and autoimmune diseases. This role is responsible for ensuring studies are delivered on time, within scope, and in compliance with regulatory standards, Good Clinical Practice (GCP), and company Standard Operating Procedures (SOPs). The Sr. CTM will partner closely with internal cross-functional teams (Clinical Development, Regulatory, Biometrics, Safety, and Quality) and external partners (CROs, vendors, and sites) to ensure operational excellence. This individual will also play a critical role in driving strategic decision-making and supporting inspection readiness and regulatory submissions. Work Arrangement the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company's discretion based on business need. Essential Duties and Responsibilities: Lead the operational strategy, planning, and execution of global Phase 1–4 clinical trials in immunology indications (e.g., autoimmune and inflammatory diseases). Serve as the primary operational point of contact for internal stakeholders and external partners. Oversee the selection and management of CROs and other vendors, including scope of work, budget development, contracting, and performance oversight. Drive site feasibility, site selection, activation, patient recruitment strategies, and ongoing site management to ensure achievement of enrollment goals. Develop and maintain study timelines, risk mitigation strategies, and operational tracking tools. Collaborate with cross-functional teams on protocol development, CRF design, ICF review, and development of operational study plans. Ensure studies are conducted in compliance with GCP/ICH guidelines, local regulatory requirements, and internal SOPs. Proactively identify and resolve operational issues, escalating risks and implementing mitigation strategies as needed. Oversee data collection activities, database lock readiness, and support data review processes. Contribute to regulatory filings, inspection readiness, and audit preparation. Provide leadership and mentorship to Clinical Operations team members. Contribute to process improvement initiatives within Clinical Operations to enhance efficiency and quality. Perform other duties and responsibilities as assigned Qualifications: Education: Bachelor’s degree in life sciences or related field (advanced degree preferred) Minimum 5 years of experience in clinical operations in the biopharmaceutical industry, with at least 3 years in a Senior CTM or equivalent leadership role. Proven track record of managing global, multi-center clinical trials in immunology or autoimmune disease indications. Experience with biologics, monoclonal antibodies, or advanced therapies. Strong knowledge of GCP/ICH guidelines, clinical trial regulations, and operational best practices. Experience in rare autoimmune indications or immune-mediated inflammatory diseases. Familiarity with adaptive trial designs or complex biomarker-driven studies. Experience in early- to late-stage development programs, including pivotal trials. Proficiency with electronic systems such as CTMS, EDC, eTMF, and risk-based monitoring tools. Ability to thrive in a fast-paced, dynamic environment and work independently with minimal supervision Excellent communication, leadership, and problem-solving skills. This position requires availability during Eastern Time (ET) business hours This role may require domestic and international travel, including overnight stays, up to 20% or more based on business needs Salary Range: The expected annual salary range for this position is listed below. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance. Salary Range $178,000—$194,500 USD Benefits: We offer a comprehensive benefits package including: Medical, Dental & Vision insurance (employee premiums 100% covered by company) 20 accrued days combined time off (PTO/Sick), 12 company holidays, & winter recharge Flexible work arrangements / hybrid schedule Health Savings Account (HSA) *Benefits are subject to eligibility requirements and plan terms. Additional details provided during the offer process* Equal Employment Opportunity: Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. Reasonable Accommodation: If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates. Privacy Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at Privacy Policy - Beeline Medicines", "summaryDescription" : "Senior Clinical Trial Manager (Lupus) at Beeline Medicines. Skills: Clinical trial operations, Global study execution, Immunology trials. Lead operational strategy. Plan clinical trials", "postedDate" : "2026-06-12T21:55:24.407", "createdAt" : "2026-06-12T21:55:24.407", "lastUpdated" : "2026-06-15T00:48:39.589", "ingestTimestamp" : "2026-06-12T21:55:24.407", "mongoId" : "6a2c5e6674d8ee00a08e3c3b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 155000, "salaryAnnualMax" : 215000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Clinical operations", "Global clinical trials", "Immunology indications", "Autoimmune diseases", "Inflammatory diseases", "Monoclonal antibodies", "Advanced therapies", "Clinical trial regulations", "Operational best practices", "Pivotal trials", "Leadership", "Problem-solving", "Clinical trial operations", "Global study execution", "Immunology trials", "Clinical trial management", "Regulatory compliance", "Vendor management", "Budget development", "Protocol development", "Risk mitigation", "Data collection", "Inspection readiness", "Audit preparation", "Study timelines", "Operational tracking", "Immunology", "Biologics", "GCP/ICH guidelines", "CTMS", "EDC", "eTMF", "Risk-based monitoring tools" ], "skillCount" : 33, "jobCategory" : "operations", "jobSubcategory" : "clinical-operations", "dataQualityScore" : 0.8888889, "_score" : 839.28705, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a2c8d9f74d8ee00a0979790", "title" : "Manager/Senior Manager, Trial Operations", "company" : "Xenon Pharmaceuticals", "industry" : "Clinical Development", "salary" : { "min" : 140200.0, "max" : 195000.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Boston", "locations" : [ "Boston" ], "timestamp" : "2026-06-15T09:50:41.454", "fingerprint" : "a8bac01751a8998fac8650cca0b26c29cfe42132faa2dff1871f3dc0f3e44f31", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/xenon/b83ed917-f851-4a2a-bfed-8b2dd29babd3/application", "externalId" : "b83ed917-f851-4a2a-bfed-8b2dd29babd3", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Boston", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "42.3588336,-71.0578303" }, { "city" : "Pawtucket", "state" : "Rhode Island", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "41.8789531,-71.3821203" } ], "locationText" : "Boston, Massachusetts, United States; Pawtucket, Rhode Island, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Data compilation", "Data review", "Data analysis", "Clinical trial set-up", "Operational support" ], "hardSkills" : [ { "name" : "Data compilation", "level" : "intermediate" }, { "name" : "Data review", "level" : "intermediate" }, { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Clinical trial set-up", "level" : "intermediate" }, { "name" : "Operational support", "level" : "intermediate" } ], "majorSkills" : "Trial operations leadership, Clinical trial management, Vendor management, Budget oversight", "majorSkillsList" : [ "Trial operations leadership", "Clinical trial management", "Vendor management", "Budget oversight" ], "coreResponsibilities" : "Provide clinical trial management leadership, Collaborate with cross-functional team members, Develop, propose, and manage plans, Lead RFP preparation, Coordinate proposal evaluation, Provide input into selection and contracting, Manage contracted service providers, Lead investigator and site selection, Review and oversee study budgets, Manage study timelines, Manage study metrics, Conduct risk assessments, Develop mitigation strategies, Develop contingency planning, Communicate with internal/external teams, Recognize challenges, Mitigate/resolve challenges, Participate in clinical trial operations, Coordinate clinical trial protocols, Write clinical trial protocols, Review clinical trial protocols, Finalize clinical trial protocols, Coordinate consent forms, Write consent forms, Review consent forms, Finalize consent forms, Coordinate study plans, Write study plans, Review study plans, Finalize study plans, Coordinate safety reviews, Write safety reviews, Review safety reviews, Finalize safety reviews, Coordinate essential regulatory documents, Write essential regulatory documents, Review essential regulatory documents, Finalize essential regulatory documents, Train new staff, Mentor new staff, Share trial conduct best practices, Implement trial conduct best practices, Oversee adherence to regulations", "teamCollaboration" : "Cross-functional team members; Internal/external teams; Multidisciplinary team", "projectManagementSkills" : [ "Project management", "Timeline management", "Budget management", "Milestone delivery" ], "domainKnowledge" : "Clinical trial regulations; ICH/GCP; US regulatory; Canadian regulatory", "domainList" : [ "clinical-trial-regulations", "ich-gcp", "us-regulatory", "canadian-regulatory" ], "domainSpecificKnowledge" : [ "Clinical trial regulations", "ICH/GCP", "US regulatory", "Canadian regulatory" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Clinical trial protocols; Consent forms; Case report forms; Study plans; Safety reviews; Regulatory documents", "continuousLearning" : "Training; Learning & Development; Tuition Assistance", "problemSolvingSkills" : "Risk assessment; Mitigation strategies; Contingency planning", "specialRequirements" : "5-10% travel", "outcomesObjectives" : "Deliver critical milestones on time; Deliver critical milestones within budget", "qualificationsBasic" : "Project management experience, Organizational skills, Ability to work independently, Ability to work collaboratively, Good judgement, Flexibility, Detail oriented", "qualificationsPreferred" : "Previous experience with CTA and IND submissions preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE https://www.nasdaq.com/market-activity/stocks/xene) is a neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization of life-changing therapeutics for patients in need. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team. What We Do: We are advancing an exciting product pipeline https://xenon-pharma.com/pipeline to address indications with high unmet medical need, including epilepsy, depression and pain. Our Phase 3 azetukalner program represents the most advanced, clinically validated potassium channel modulator in late-stage clinical development for multiple indications. In March 2026, we announced positive topline data from our Phase 3 X-TOLE2 study of azetukalner in focal onset seizures (FOS), and we anticipate submitting a New Drug Application to the Food and Drug Administration in the third quarter of 2026. Our Phase 3 epilepsy program also includes a second FOS study, X-TOLE3, which would support regulatory submissions outside the U.S., and the X-ACKT study in primary generalized tonic-clonic seizures, which would support regulatory submissions for an additional epilepsy indication. We also have multiple Phase 3 azetukalner clinical trials underway in major depressive disorder (MDD) and bipolar depression (BPD), based on topline data from our Phase 2 X-NOVA clinical trial. In addition, we are proud of our strong heritage in human genetics, deep understanding of ion channel biology, and expertise in novel chemistries to enable potent, selective ion channel targeting. We continue to advance an early-stage pipeline of novel therapeutic candidates, including Phase 1 studies for XEN1701 (targeting Nav1.7) and XEN1120 (targeting Kv7), which are important pain targets. Backed by a strong balance sheet to support our growth plans, we continue to build a fully integrated, premier neuroscience company with strong discovery, clinical development, corporate, and commercial operations. About the Role: We are seeking a Senior Manager, Trial Operations to join our team. This person may work flexibly across a number of clinical stage trials and projects, acting as a study lead and manager for select clinical trial and be hands-on in data compilation, review and analysis, clinical trial set-up and management, and operational support activities. This is an excellent opportunity for someone with strong organizational skills and the ability to work independently on a variety of tasks and projects. In addition, the successful candidate must have strong project management experience, excellent verbal and written communication, an ability to work collaboratively, demonstrate good judgement, and be flexible and detail oriented. This position reports to the Director, Trial Operations, and will be based out of Boston, MA, USA in our Needham office. We may consider remote locations for exceptional candidates. This is a Hybrid position requiring a minimum of two onsite days per week. RESPONSIBILITIES: - Provide clinical trial management leadership for multiple Phase 3 studies, across therapeutic areas. - Collaborate with cross-functional team members to ensure highly integrated plans and documents for clinical trials. - Develop, propose, and manage plans for assigned studies and activities. - Lead the preparation of Requests for Proposals (RFPs) in collaboration with other internal team members, coordinate the evaluation of proposals and provide input into the selection and contracting of Contract Research Organizations (CRO) and other clinical service providers. - Manage contracted service providers to deliver against the contracts. - Lead the selection of qualified investigators and study sites in collaboration with the Clinical Development team. - Review and oversee study budgets and invoices to ensure vendors are invoicing in accordance with their contracts. - Develop and manage study timeline and study metrics cross-functionally. - Conduct risk assessments, mitigation strategies and contingency planning. - Communicate with internal/external teams to proactively recognize challenges and work cross-functionally on strategies to mitigate/resolve. - Actively participate in all aspects of clinical trial operations, including the coordination, writing, review and/or finalization of clinical trial protocols, consent forms, case report forms, study plans, safety reviews and other essential regulatory documents. - Train and mentor new staff or peer mentorship of new hires. - Actively participates in documentation, sharing and implementation of trial conduct best practices and lessons learned with junior staff. - Oversee adherence to applicable regulations, recognized guidelines, clinical trial protocol, and standards of clinical practice. - Participate in the development and updating of standard operating procedures as required. - Act in accordance with Company policies, including, for example, the Code of Business Conduct and Ethics. - Other duties as assigned. QUALIFICATIONS: - A minimum bachelor’s degree in a scientific discipline and/or other healthcare designation (e.g., RN). - A minimum of 5-8 years clinical project/study management experience within the pharmaceutical and/or biotechnology/biopharmaceutical industry or at a CRO. Job level will be commensurate with experience. - Ability to lead cross-functional team through all activities in the full clinical study life cycle. - Strong vendor management skills and experience managing outsourced work. - A good understanding of all phases of the drug development process and the interdependencies between Clinical and other functional areas (e.g., CMC, nonclinical/toxicology, Regulatory Affairs etc.), with specific experience in phase 3 clinical trials preferred. - Demonstrated ability to successfully work across a variety of teams and manage multiple conflicting priorities. - Demonstrated ability to successfully manage and deliver on critical milestones in the successful completion of clinical trials on time and within budget. - Strong knowledge and understanding of ICH/GCP and US and Canadian regulatory environments; a comprehensive understanding of clinical trial regulations across multiple jurisdictions with previous experience with CTA and IND submissions preferred. - Excellent oral and written communication skills. - Strong interpersonal skills and ability to foster strong collaborative relationships with internal and external team members. - Ability to work both independently and collaboratively as part of a multidisciplinary team. - Exceptional attention to detail and excellent organizational skills. - Ability to thrive in a dynamic and fast-paced environment. - Ability to prioritize duties and manage multiple matters from start to finish with minimal supervision and with a demonstrated ability to lead change and make independent decisions. - Ability to handle highly confidential and sensitive materials and information with complete discretion. - Ability and willingness to travel 5-10% of the time (internationally and domestic) To apply for this position, click Apply Now to complete the application. We thank all applicants for their interest; however, due to the volume of applicants, only those chosen for interview will be contacted. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions. Xenon encourages time to rest and re-charge through vacation, personal days, sick days, and an end-of-year company shutdown. Xenon highly values employee development and has an expanding Training, Learning & Development program, including a Tuition Assistance program for advanced degrees.", "summaryDescription" : "Manager/Senior Manager, Trial Operations at Xenon Pharmaceuticals. Skills: Trial operations leadership, Clinical trial management, Vendor management, Budget oversight. Provide clinical trial management leadership. 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Medical science; Life science", "domainList" : [ "clinical-data-management", "medical-science", "life-science" ], "domainSpecificKnowledge" : [ "Clinical data management", "Medical science", "Life science" ], "toolProficiency" : [ "TMF", "ETMF" ], "communicationSkills" : "Communication line", "documentationSkills" : "Study documentation; CRF Completion Guidelines; Data Management Plan; Edit Checks Specification; User Access Management Plan; Data Validation Plan; External Data Transfer Agreements; SAE Reconciliation Guidelines; Local Lab Normal Ranges Guidelines; Coding Guidelines", "problemSolvingSkills" : "Query management", "qualificationsBasic" : "College or University degree, Minimum of one year of industry experience, Experience working with clinical or medical data", "qualificationsPreferred" : "PhD preferred, Specific ML framework experience, Cloud platform certs", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,200 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them. 1. Acts as a communication line for project teams regarding clinical data management 2. Maintains TMF/eTMF 3. Trains Assistant Data Manager 4. Is involved in clinical data management activities including, but not limited to: * Supporting development of study documentation (eCRF Requirements, Edit Checks Specification, Data Management Plan, CRF Completion Guidelines, User Access Management Plan, Data Validation Plan, External Data Transfer Agreements, SAE Reconciliation Guidelines, Local Lab Normal Ranges Guidelines, Coding Guidelines where applicable) * User acceptance testing * User access management * Data review * eCRF/External data reconciliation * Medical coding (for staff with medical/Life Science background) * Supporting SAE reconciliation * Query management * Local lab normal ranges entry and QC * Study Database Lock activities * Archival of CRFs QC * Data entry/QC * Project status reporting * Data listings/Patient profiles generation and delivery * Assisting with Database Lock tasks as needed for assigned projects ## Qualifications * College or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities * A minimum of one year of industry experience, preferably working with clinical or medical data", "summaryDescription" : "Data Manager for Clinical Trials at PSI CRO. Skills: Data management, Clinical trials, Data quality, Database administration. Act as communication line for project teams. Maintain TMF/eTMF", "postedDate" : "2026-06-12T20:35:30.000", "createdAt" : "2026-06-16T00:25:49.908", "lastUpdated" : "2026-06-16T10:38:08.200", "ingestTimestamp" : "2026-06-16T00:25:49.908", "mongoId" : "6a305e6cf292fd229cf70714", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Statistical analysis", "Regression", "Classification", "Clustering", "Time-series analysis", "A/B testing", "Causal inference", "Data management", "Clinical trials", "Data quality", "Database administration", "Clinical data management", "Data reconciliation", "Medical coding", "Query management", "Database lock", "Project status reporting", "Medical science", "Life science", "TMF", "ETMF" ], "skillCount" : 21, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 828.96014, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2cb20e74d8ee00a09df75e", "title" : "Principal, Global Feasibility (pre-award strategy)", "industry" : "Analyst", "salary" : { "min" : 130000.0, "max" : 180000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Principal, Global Feasibility role in the Biotech industry in France, adjusted for seniority and industry." }, "location" : "France", "locations" : [ "France" ], "timestamp" : "2026-06-16T05:34:49.781", "fingerprint" : "596d336783c0be945cf2ad49d6c244cf7e320ff2069cd90a10f0183041a7284b", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/988530f1-909a-470e-a441-571d7f588a67/apply", "externalId" : "988530f1-909a-470e-a441-571d7f588a67", "industryFunction" : { }, "structuredLocations" : [ { "country" : "France", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "France", "employmentType" : "FULL_TIME", "minimumEducation" : "BS/RN/MS", "experienceMinYears" : 3, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Feasibility assessments", "Pre-award strategy", "RFP analysis", "Partnership feasibility", "Site-level analysis", "Data management", "Process improvement", "Methodology development" ], "hardSkillsList" : [ "Scientific research", "Evidence-based decisions" ], "softSkillsList" : [ "Autonomy" ], "hardSkills" : [ { "name" : "Scientific research", "level" : "intermediate" }, { "name" : "Evidence-based decisions", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Autonomy" } ], "majorSkills" : "Global feasibility, Pre-award strategy, Clinical trial execution, Stakeholder engagement", "majorSkillsList" : [ "Global feasibility", "Pre-award strategy", "Clinical trial execution", "Stakeholder engagement" ], "coreResponsibilities" : "Lead feasibility assessments, Deliver feasibility assessments, Deliver pre-award strategy assessments, Develop site-level feasibility outputs, Analyze site-level feasibility outputs, Present site-level feasibility outputs, Design feasibility strategies, Identify innovative solutions, Propose innovative solutions, Conduct advanced research, Support bid defense preparation, Participate in client-facing meetings, Maintain accurate documentation, Ensure high-quality data management, Contribute to departmental metrics, Contribute to feasibility frameworks, Contribute to process improvements, Mentor junior team members, Support junior team members, Provide guidance on analysis, Provide guidance on reporting, Provide guidance on best practices, Participate in strategic initiatives, Evaluate data assets", "teamCollaboration" : "Cross-functional teams; Global teams", "domainKnowledge" : "Clinical research; Global clinical feasibility; Country selection; Site selection; Drug development lifecycle; Therapeutic areas", "domainList" : [ "clinical-research", "global-clinical-feasibility", "country-selection", "site-selection", "drug-development-lifecycle", "therapeutic-areas" ], "domainSpecificKnowledge" : [ "Clinical research", "Global clinical feasibility", "Country selection", "Site selection", "Drug development lifecycle", "Therapeutic areas" ], "communicationSkills" : "Written communication; Verbal communication; Presentation abilities", "documentationSkills" : "Accurate documentation", "continuousLearning" : "Continuous learning opportunities; Professional development support", "innovationCreativity" : "Innovative solutions", "problemSolvingSkills" : "Problem-solving skills; Synthesize complex data", "outcomesObjectives" : "Enhance operational efficiency", "qualificationsBasic" : "BS/RN/MS with 7+ years experience, PhD/MD with 3+ years experience, Clinical research background, GCP understanding, Study start-up processes, Global clinical feasibility knowledge, Country and site selection knowledge, Drug development lifecycle knowledge, Manage complex workloads, Manage multi-study workloads, Manage under tight deadlines, High attention to detail, Analytical thinking skills, Strategic thinking skills, Problem-solving skills, Synthesize complex data sets, Excellent communication skills, Written communication abilities, Verbal communication abilities, Presentation abilities, Senior stakeholder engagement, Influence effectively, Negotiate effectively, Work effectively in global teams, Work effectively in cross-functional teams, Customer-facing roles experience, Consultancy-style roles experience, Mentor junior colleagues, Support junior colleagues, Contribute to team capability development, Organizational skills, Manage competing priorities", "qualificationsPreferred" : "Experience in life sciences environments", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "## Accountabilities Lead and independently deliver highly complex global feasibility and pre-award strategy assessments across all therapeutic areas, including RFP and partnership feasibility work. Develop, analyze, and present site-level feasibility outputs in both written and presentation formats for internal and external stakeholders. Collaborate cross-functionally with business development, medical directors, business analysts, and operational teams to design optimal feasibility strategies. Identify and propose innovative solutions for non-standard or complex feasibility requests with minimal supervision. Conduct advanced research using scientific literature, internal data systems, and external sources to support evidence-based feasibility decisions. Support bid defense preparation and participate in client-facing meetings with a high level of professionalism and autonomy. Maintain accurate documentation and ensure high-quality data management within internal systems and knowledge repositories. Contribute to the development of departmental metrics, feasibility frameworks, and process improvements to enhance operational efficiency. Mentor and support junior and mid-level team members, providing guidance on analysis, reporting, and best practices. Participate in strategic initiatives, including system development, data asset evaluation, and continuous improvement of feasibility methodologies. Requirements Advanced degree in Life Sciences or related field (BS/RN/MS with 7+ years of experience, or PhD/MD with 3+ years of relevant experience). Strong background in clinical research, including clinical trial execution, GCP understanding, and study start-up processes. Deep knowledge of global clinical feasibility, country and site selection, and drug development lifecycle. Proven ability to independently manage complex, multi-study workloads under tight deadlines while maintaining high attention to detail. Strong analytical, strategic thinking, and problem-solving skills with the ability to synthesize complex data sets into clear insights. Excellent communication skills, including written, verbal, and presentation abilities for senior stakeholder engagement. Demonstrated ability to influence, negotiate, and work effectively in cross-functional, global teams. Experience in customer-facing or consultancy-style roles within clinical research or life sciences environments. Ability to mentor and support junior colleagues while contributing to team capability development. Strong organizational skills with the ability to manage competing priorities in a fast-paced environment. Benefits Competitive compensation and comprehensive global benefits package. Opportunity to work on high-impact, global clinical research programs across multiple therapeutic areas. Strong career development and advancement opportunities within a leading life sciences environment. Exposure to cutting-edge clinical development strategies and global feasibility operations. Collaborative, international, and science-driven work culture. Flexible working arrangements supporting work-life balance. Continuous learning opportunities, including training and professional development support. Participation in high-visibility projects influencing global drug development success. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Principal, Global Feasibility (pre-award strategy). Skills: Global feasibility, Pre-award strategy, Clinical trial execution, Stakeholder engagement. Lead feasibility assessments. Deliver feasibility assessments", "postedDate" : "2026-06-12T12:29:46.542", "createdAt" : "2026-06-12T12:29:46.542", "lastUpdated" : "2026-06-16T05:34:49.781", "ingestTimestamp" : "2026-06-14T21:39:22.737", "mongoId" : "6a2cb20e74d8ee00a09df75e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Scientific research", "Evidence-based decisions", "Autonomy", "Global feasibility", "Pre-award strategy", "Clinical trial execution", "Stakeholder engagement", "Feasibility assessments", "RFP analysis", "Partnership feasibility", "Site-level analysis", "Data management", "Process improvement", "Methodology development", "Clinical research", "Global clinical feasibility", "Country selection", "Site selection", "Drug development lifecycle", "Therapeutic areas" ], "skillCount" : 20, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "_score" : 827.9154, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2d3f1074d8ee00a0b347f0", "title" : "Data Manager for Clinical Trials", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 75000.0, "max" : 95000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Data Manager in Mississauga, Canada, adjusted for the Biotech industry and full-time employment." }, "location" : "Mississauga, ON, Canada", "locations" : [ "Mississauga", "ON", "Canada" ], "timestamp" : "2026-06-16T06:35:51.865", "fingerprint" : "cfd7cbd62c3d5a4fc465804d775363e78d15585f2522790f8f1a3777acb0cd35", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000131986259-data-manager-for-clinical-trials", "externalId" : "744000131986259", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Mississauga", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.5884727,-79.6436580" } ], "locationText" : "Mississauga, Ontario, Canada", "employmentType" : "FULL_TIME", "minimumEducation" : "College or University degree", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "professionalSkills" : [ "Clinical data management", "Medical coding" ], "hardSkillsList" : [ "Data management", "Data reconciliation", "Query management", "Data entry", "Data listings", "Patient profiles generation" ], "hardSkills" : [ { "name" : "Data management", "level" : "intermediate" }, { "name" : "Data reconciliation", "level" : "intermediate" }, { "name" : "Query management", "level" : "intermediate" }, { "name" : "Data entry", "level" : "intermediate" }, { "name" : "Data listings", "level" : "intermediate" }, { "name" : "Patient profiles generation", "level" : "intermediate" } ], "majorSkills" : "Clinical data management, Data reconciliation, Query management", "majorSkillsList" : [ "Clinical data management", "Data reconciliation", "Query management" ], "coreResponsibilities" : "Act as communication line for project teams, Maintain TMF/eTMF, Train Assistant Data Manager, Support development of study documentation, Manage user access, Review data, Reconcile eCRF/External data, Support SAE reconciliation, Manage queries, Enter and QC local lab normal ranges, Perform Study Database Lock activities, QC archival of CRFs, Perform data entry/QC, Report project status, Generate and deliver data listings/Patient profiles, Assist with Database Lock tasks", "teamCollaboration" : "Project teams", "domainKnowledge" : "Clinical data management; Medical science; Life Science", "domainList" : [ "clinical-data-management", "medical-science", "life-science" ], "domainSpecificKnowledge" : [ "Clinical data management", "Medical science", "Life Science" ], "toolProficiency" : [ "ECRF", "TMF", "ETMF" ], "communicationSkills" : "Communication line", "documentationSkills" : "Study documentation; CRF Completion Guidelines; Data Management Plan; Edit Checks Specification; User Access Management Plan; Data Validation Plan; External Data Transfer Agreements; SAE Reconciliation Guidelines; Local Lab Normal Ranges Guidelines; Coding Guidelines", "qualificationsBasic" : "College or University degree, Minimum of one year of industry experience, Experience working with clinical or medical data", "qualificationsPreferred" : "PhD preferred, Specific ML framework experience, Cloud platform certs", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,200 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them. 1. Acts as a communication line for project teams regarding clinical data management 2. Maintains TMF/eTMF 3. Trains Assistant Data Manager 4. Is involved in clinical data management activities including, but not limited to: * Supporting development of study documentation (eCRF Requirements, Edit Checks Specification, Data Management Plan, CRF Completion Guidelines, User Access Management Plan, Data Validation Plan, External Data Transfer Agreements, SAE Reconciliation Guidelines, Local Lab Normal Ranges Guidelines, Coding Guidelines where applicable) * User acceptance testing * User access management * Data review * eCRF/External data reconciliation * Medical coding (for staff with medical/Life Science background) * Supporting SAE reconciliation * Query management * Local lab normal ranges entry and QC * Study Database Lock activities * Archival of CRFs QC * Data entry/QC * Project status reporting * Data listings/Patient profiles generation and delivery * Assisting with Database Lock tasks as needed for assigned projects ## Qualifications * College or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities * A minimum of one year of industry experience, preferably working with clinical or medical data", "summaryDescription" : "Data Manager for Clinical Trials at PSI CRO. Skills: Clinical data management, Data reconciliation, Query management. Act as communication line for project teams. Maintain TMF/eTMF", "postedDate" : "2026-06-12T20:35:30.000", "createdAt" : "2026-06-14T20:28:47.999", "lastUpdated" : "2026-06-16T06:35:51.865", "ingestTimestamp" : "2026-06-14T20:28:47.999", "mongoId" : "6a2d3f1074d8ee00a0b347f0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Data management", "Data reconciliation", "Query management", "Data entry", "Data listings", "Patient profiles generation", "Clinical data management", "Medical coding", "Medical science", "Life Science", "ECRF", "TMF", "ETMF" ], "skillCount" : 13, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 822.9836, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3091ccf292fd229c0bffdb", "title" : "Clinical Study Coordinator", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Clinical Study Coordinator in Chicago, USA, adjusted for mid-seniority and full-time employment in the healthcare industry." }, "location" : "South Cook/Will County, Chicago, Illinois, United States", "locations" : [ "South Cook/Will County, Chicago", "Illinois", "United States" ], "certifications" : [ "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization" ], "timestamp" : "2026-06-16T13:21:50.873", "fingerprint" : "b7170833b4223279c19879a9283ea28c5f24522062c7ea8ef1b518fbe9ae4b89", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000132293919-clinical-study-coordinator-", "externalId" : "744000132293919", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chicago", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.8755616,-87.6244212" } ], "locationText" : "Chicago, Illinois, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Study conduct tasks", "Data entry", "Monitoring visits", "Mentoring staff", "Administrative tasks", "Patient recruitment", "Patient identification", "Informed consent", "Laboratory testing", "Investigational products", "Clinical supplies", "Temperature monitoring", "Contract negotiations", "Budget negotiations", "Investigator payments", "Staff training", "Study documents", "Regulatory documents", "Site improvements" ], "hardSkillsList" : [ "Protocol adherence", "Data query resolution", "Adverse event reporting", "Protocol deviation reporting", "Investigational product handling", "Site SOP adherence", "Regulatory agency inspections" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Protocol adherence", "level" : "intermediate" }, { "name" : "Data query resolution", "level" : "intermediate" }, { "name" : "Adverse event reporting", "level" : "intermediate" }, { "name" : "Protocol deviation reporting", "level" : "intermediate" }, { "name" : "Investigational product handling", "level" : "intermediate" }, { "name" : "Site SOP adherence", "level" : "intermediate" }, { "name" : "Regulatory agency inspections", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Clinical trial coordination, Site support, Regulatory compliance", "majorSkillsList" : [ "Clinical trial coordination", "Site support", "Regulatory compliance" ], "coreResponsibilities" : "Support medical institution in clinical trial activities, Assess feasibility of clinical studies, Conduct research-related visits, Assist with logistics of scheduling research visits, Assist with testing per schedule of events, Collaborate with ancillary departments, Assist with data entry into EDC systems, Contact CRO or sponsor representatives, Schedule monitoring visits, Resolve study specific issues, Mentor staff, Perform administrative tasks, Act as communication line, Facilitate evaluation of proposed studies, Provide responses to feasibility questions, Participate in patient recruitment/identification, Confirm eligibility for study inclusion, Assist with plan development for recruitment tools, Assist with plan development for retention tools, Assist with plan development for source documentation, Assist with plan development for site tools, Assist research team in obtaining informed consent, Obtain required assessments at each visit, Notify investigator of critical values, Obtain laboratory testing, Process laboratory testing, Ship laboratory testing, Assist in scheduling sponsor visits, Assist in preparation for sponsor visits, Assist in scheduling CRO representative visits, Assist in preparation for CRO representative visits, Track patient recruitment, Track patient enrollment, Support medical site team, Ensure enrollment targets are met, Provide updates on study amendments, Ensure accurate data entry, Ensure timely data entry, Resolve data queries, Assist in reporting adverse events, Assist in reporting protocol deviations, Support handling of investigational products, Support accountability of investigational products, Support reconciliation of investigational products, Maintain study blinding, Assist site staff with temperature monitoring, Support contract negotiations, Support budget negotiations, Oversee Investigator/Site Payments, Ensure staff complete training, Complete retraining for protocol changes, Ensure investigator reviews study documents, Ensure investigator signs study documents, Provide guidance on conducting clinical trials, Maintain study documents, Prepare for on-site study visits, Prepare for audits, Prepare for regulatory agency inspections, Prepare and submit regulatory documents, Prepare and submit correspondence to regulatory authorities, Prepare and submit correspondence to institutional review boards, Involved in on-site training of additional staff, Identify areas needing improvement, Develop tools for site improvements, Maintain licensure, Maintain certifications", "teamCollaboration" : "Cross-functional departments; Ancillary departments; CRO representatives; Sponsor representatives; Medical institution staff; Research staff; Site staff; Milestone One Manager", "domainKnowledge" : "Clinical trial conduct; Human subjects research; Local laws and regulations; Federal laws and regulations; Study protocols; Schedule of events; Inclusion and exclusion criteria; Site SOPs; Study-specific lab manuals; Investigational products; Clinical supplies; Study blinding; Regulatory authorities; Institutional review boards (IRBs)", "domainList" : [ "clinical-trial-conduct", "human-subjects-research", "local-laws-and-regulations", "federal-laws-and-regulations", "study-protocols", "schedule-of-events", "inclusion-and-exclusion-criteria", "site-sops", "study-specific-lab-manuals", "investigational-products", "clinical-supplies", "study-blinding", "regulatory-authorities", "institutional-review-boards-irbs" ], "domainSpecificKnowledge" : [ "Clinical trial conduct", "Human subjects research", "Local laws and regulations", "Federal laws and regulations", "Study protocols", "Schedule of events", "Inclusion and exclusion criteria", "Site SOPs", "Study-specific lab manuals", "Investigational products", "Clinical supplies", "Study blinding", "Regulatory authorities", "Institutional review boards (IRBs)" ], "toolProficiency" : [ "EDC systems" ], "communicationSkills" : "Line of communication", "documentationSkills" : "Source documentation; Study documents; Regulatory documents", "innovationCreativity" : "Develop tools to assist with improvements", "problemSolvingSkills" : "Resolve study specific issues; Resolve data queries", "specialRequirements" : "On-site position", "outcomesObjectives" : "Ensure responses to feasibility questions are provided in due time; Ensure enrollment targets are met at the site level; Ensure accurate and timely data entry; Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial; Ensure the investigator reviews and signs study documents appropriately and within a reasonable period", "qualificationsBasic" : "2 years experience coordinating clinical research studies, Current Good Clinical Practice (GCP), International Air Transport Association (IATA), Current Basic Cardiopulmonary Resuscitation (CPR), Phlebotomy certification unless part of active professional licensure (RN or LPN)", "qualificationsPreferred" : "Nephrology experience, Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. Tasks may include activities associated with the assessment of the feasibility of new/potential clinical studies, conducting research-related visits as outlined in the respective protocol, assisting the site with logistics of scheduling research visits and testing per the schedule of events in the protocol, collaboration with ancillary departments involved in the research visit to assist in a smooth patient flow at research visits., general study conduct tasks, assistance with data entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In addition, mentoring staff and administrative tasks as assigned by the Milestone One Manager. In this job you will: * Acts as a constant line of communication between Milestone One, the Sponsor or CRO, and the medical institution. * Facilitates the evaluation of proposed studies and ensures responses to feasibility questions are provided in due time. * Actively participates in patient recruitment/identification and evaluation for study inclusion by confirming eligibility according to the Inclusion and exclusion criteria. * Assists with plan development for new recruitment / retention tools, source documentation and other site tools to enhance quality and time management of research staff. * Assists the local research team in obtaining informed consent before study entry or any study-related procedures or tests being performed. * Assist with obtaining the required assessments at each visit per the protocol and notify the investigator of any critical values that need immediate attention or would prohibit or delay study treatment. * Assist with obtaining local and central laboratory testing, processing, and shipping per site SOP and study-specific lab manual. * Assist in scheduling and preparation for all types of sponsors or CRO representative visits at the medical institution. * Track patient recruitment and enrollment and actively supports the medical site team to ensure enrollment targets are met at the site level. Provides regular updates to the staff and investigators regarding study amendments. * Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to guidelines and investigator instructions. * Support proper handling, accountability, and reconciliation of all investigational products and clinical supplies. If applicable, always maintain the study blinding. Protocol and sponsor/CRO guidance will be followed if a study participant requires unblinding. * Assist site staff with maintaining appropriate temperature monitoring for study products and supplies. * Support the contract and budget negotiations and oversees Investigator/Site Payments. * Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial. Retraining will be completed for changes to the protocol before site implementation. * Be responsible for ensuring the investigator reviews and signs study documents appropriately and within a reasonable period. Guidance should be provided to educate the site research team on requirements for conducting clinical trials, date format, etc. * Actively participate in maintaining study documents at the medical institution in preparation for on-site study visits/audits or regulatory agency inspections. * Assist with preparing and submitting regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs). * May be involved in the on-site training of additional staff as part of the SEO or other education programs. * Assist with identifying areas that need improvement for specific sites and assists with developing tools to assist with improvements. * Maintain all licensure and certifications applicable to the role of SEO site/Study coordinator II. * SEO SC is responsible for only performing assigned tasks within their training and licensure if applicable. SEO SC should immediately consult the assigned Milestone One manager for tasks that do not fall within their scope. ## Qualifications Education Relevant education and at least two years of experience coordinating clinical research studies involving human subjects OR, if allowed by local regulations, on-the-job training with at least two years of experience coordinating clinical research studies involving human subjects. Nephrology experience preferred. Certifications * Current Good Clinical Practice (GCP) * International Air Transport Association (IATA) * Current Basic Cardiopulmonary Resuscitation (CPR) * Phlebotomy certification unless part of active professional licensure (RN or LPN) * Preferred Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization. May be obtained within (1) year of employment or status change if not currently certified. ## Additional Information Located in South Cook/ Will County, Chicago (On-site position). If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you!", "summaryDescription" : "Clinical Study Coordinator at PSI CRO. Skills: Clinical trial coordination, Site support, Regulatory compliance. Support medical institution in clinical trial activities. Assess feasibility of clinical studies", "postedDate" : "2026-06-15T22:35:56.000", "createdAt" : "2026-06-16T03:37:36.816", "lastUpdated" : "2026-06-16T13:21:50.873", "ingestTimestamp" : "2026-06-16T03:37:36.816", "mongoId" : "6a3091ccf292fd229c0bffdb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Protocol adherence", "Data query resolution", "Adverse event reporting", "Protocol deviation reporting", "Investigational product handling", "Site SOP adherence", "Regulatory agency inspections", "Leadership", "Clinical trial coordination", "Site support", "Regulatory compliance", "Study conduct tasks", "Data entry", "Monitoring visits", "Mentoring staff", "Administrative tasks", "Patient recruitment", "Patient identification", "Informed consent", "Laboratory testing", "Investigational products", "Clinical supplies", "Temperature monitoring", "Contract negotiations", "Budget negotiations", "Investigator payments", "Staff training", "Study documents", "Regulatory documents", "Site improvements", "Clinical trial conduct", "Human subjects research", "Local laws and regulations", "Federal laws and regulations", "Study protocols", "Schedule of events", "Inclusion and exclusion criteria", "Site SOPs", "Study-specific lab manuals", "Study blinding", "Regulatory authorities", "Institutional review boards (IRBs)", "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "EDC systems" ], "skillCount" : 48, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "_score" : 819.9726, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a3fb574d8ee00a05c465e", "title" : "Clinical Trial Manager", "company" : "Precision Medicine Group", "industry" : "Life Sciences", "salary" : { "min" : 450000.0, "max" : 750000.0, "currency" : "CNY", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Clinical Trial Manager in China, adjusted for the biotech industry and remote work." }, "location" : "Remote (China)", "locations" : [ "Remote (China)" ], "timestamp" : "2026-06-11T07:50:44.742", "fingerprint" : "3ad6e88d5e1e9a20fe8ae8193933eaf0afc10f8db376a2ecc84f38f979c36fd7", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/precisionmedicinegroup/jobs/6016951004", "externalId" : "6016951004", "industryFunction" : { }, "structuredLocations" : [ { "country" : "China", "continent" : "as", "workMode" : "remote" } ], "locationText" : "China", "experienceLevel" : "Manager", "professionalSkills" : [ "Clinical trial execution", "Scientific knowledge", "Laboratory expertise", "Data sciences" ], "hardSkillsList" : [ "Clinical monitoring", "Protocol development", "Regulatory requirements", "Site feasibility", "Enrollment strategy", "Vendor management", "Data quality", "Data cleaning" ], "hardSkills" : [ { "name" : "Clinical monitoring", "level" : "intermediate" }, { "name" : "Protocol development", "level" : "intermediate" }, { "name" : "Regulatory requirements", "level" : "intermediate" }, { "name" : "Site feasibility", "level" : "intermediate" }, { "name" : "Enrollment strategy", "level" : "intermediate" }, { "name" : "Vendor management", "level" : "intermediate" }, { "name" : "Data quality", "level" : "intermediate" }, { "name" : "Data cleaning", "level" : "intermediate" } ], "majorSkills" : "Clinical trial management, Protocol adherence, Regulatory compliance", "majorSkillsList" : [ "Clinical trial management", "Protocol adherence", "Regulatory compliance" ], "coreResponsibilities" : "Serve as clinical trial lead, Plan clinical studies, Conduct clinical studies, Oversee clinical studies, Ensure protocol adherence, Ensure SOP adherence, Ensure GCP adherence, Ensure regulatory adherence, Act as primary clinical point of contact, Collaborate on invoicing, Manage clinical budget variance, Develop study related documents, Identify training needs for CRAs, Identify training needs for vendors, Present at Investigator Meetings, Present at Study Kick-off meetings, Generate potential site list, Drive site feasibility process, Identify risks to enrollment targets, Develop country recruitment strategy, Develop country retention strategy, Develop communication with investigators, Develop relationships with investigators, Ensure effective site feasibility, Ensure effective site start up, Ensure effective enrollment, Ensure effective site maintenance, Ensure effective site close out, Lead internal clinical team meetings, Set expectations for clinical team, Address CRA questions, Address site questions, Maintain FAQ log, Support investigator meetings, Review IP release packages, Approve IP release packages, Oversee submissions to Competent Authorities, Oversee approvals to Competent Authorities, Oversee submissions to IRB/Ethics Committees, Oversee approvals to IRB/Ethics Committees, Develop clinical monitoring strategies, Assure study timelines are met, Assure quality deliverables, Generate metric reporting, Utilize metric reporting, Ensure study is conducted per plan, Communicate issues to PM, Communicate issues to CRAs, Implement eTMF, Manage eTMF, Develop CAPA, Implement CAPA, Close CAPA, Assist sites with GCP audits, Assist internal staff with GCP audits, Assist CRAs with GCP audits, Address project-specific resourcing issues, Escalate CRA performance issues, Escalate site compliance issues, Ensure data quality, Ensure compliance with data cleaning timelines, Manage investigational product processes, Manage drug accountability, Manage drug reconciliation, Assume project management responsibility, Support business development activities, Support marketing activities, Negotiate site budget, Negotiate investigator contract, Review site visit reports, Ensure monitoring is executed per plan, Manage clinical vendors, Perform clinical data review, Generate query, Manage workload of supervised staff, Perform other duties as assigned", "teamCollaboration" : "Internal clinical team; CRAs; CTAs; Data management; QA; Regulatory departments; Legal department; Site contracts group", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Oncology; Rare Disease; ICH-GCP; Clinical trial monitoring; Clinical documentation; Investigational product", "domainList" : [ "oncology", "rare-disease", "ich-gcp", "clinical-trial-monitoring", "clinical-documentation", "investigational-product" ], "domainSpecificKnowledge" : [ "Oncology", "Rare Disease", "ICH-GCP", "Clinical trial monitoring", "Clinical documentation", "Investigational product" ], "toolProficiency" : [ "CTMS", "eTMF" ], "communicationSkills" : "Presenting at meetings", "documentationSkills" : "Clinical documents; CRF completion guidelines; Study trackers; Training materials; FAQ log", "problemSolvingSkills" : "Risk identification; Problem resolution", "qualificationsBasic" : "Bachelor's degree or equivalent, 5-8 years clinical research experience, Significant clinical monitoring experience", "qualificationsPreferred" : "Advanced degree preferred, Oncology (Phase I) trial experience in Taiwan and China preferred", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease. We are hiring for a Clinical Trial Manager (based in Shanghai/Beijing) Position Summary: Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies per defined scope of work and ensures that clinical studies are conducted in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP and all applicable regulatory requirements. Essential functions of the job include but are not limited to: Primary clinical point of contact with the client Collaborate with PM on monthly invoicing and variance management of clinical budget Develop study related clinical documents (e. g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials) Identify and develop training needs for CRAs and third-party vendors specific to the study, protocol and practices including presenting these at Investigator Meetings and Study Kick-off meetings Generate potential site list from key stakeholders and drive site feasibility process Identify potential risks to the enrollment targets based on feasibility analysis and site’s contracted commitment Develop and finalize the country recruitment/retention strategy Develop timely and effective communication and good working relationships with investigators and study team to ensure effective and timely feasibility, site start up, enrollment, maintenance and close out procedures Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs Address all CRA and site questions and maintains Frequently Asked Question (FAQ) log as appropriate Support in planning and conducting investigator meetings Review and/or approve of IP release packages Oversee, support and track all submissions and approvals to Competent Authorities and IRB/Ethics Committees in conjunction with regulatory departments as applicable Develop clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables Generate and utilize metric reporting (e. g. CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicates issues to PM and CRAs as appropriate Responsible for eTMF implementation and management Collaborate with PM, CRAs and QA to develop any Corrective and Preventative Action Plan (CAPA) and is accountable for implementation and timely closure Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits Work closely with PM for project-specific resourcing issues Escalate pertinent CRA performance and site compliance issues when necessary Collaborate with data management and CRAs to ensure data quality and compliance with data cleaning timelines Manage processes for investigational product (IP) including drug accountability and reconciliation When a cross-functional PM is not assigned to a given program, the CTM will assume project management responsibility as needed Supports business development and marketing activities as appropriate May negotiate site budget and investigator contract with support from the legal department and/or site contracts group May review site visit reports and ensures monitoring (i. e. scheduling and scope) is executed per monitoring plan May be responsible for management of clinical vendors (e. g. labs, IP, patient diary, home health care) in conjunction with PM May perform clinical data review of patient profiles, data listings and summary tables, including query generation May have line management responsibilities May manages workload of supervised staff with continued assessment and adjustment as needed Perform other duties as assigned by management Qualifications: Minimum Required : Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred Minimum of 5-8 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience. Oncology (Phase I) trial experience in Taiwan and China preferred Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.", "summaryDescription" : "Clinical Trial Manager at Precision Medicine Group. Skills: Clinical trial management, Protocol adherence, Regulatory compliance. Serve as clinical trial lead. Plan clinical studies", "postedDate" : "2026-06-11T07:12:27.383", "createdAt" : "2026-06-11T07:12:27.383", "lastUpdated" : "2026-06-11T07:50:44.742", "ingestTimestamp" : "2026-06-11T07:12:27.383", "mongoId" : "6a2a3fb574d8ee00a05c465e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Clinical monitoring", "Protocol development", "Regulatory requirements", "Site feasibility", "Enrollment strategy", "Vendor management", "Data quality", "Data cleaning", "Clinical trial management", "Protocol adherence", "Regulatory compliance", "Clinical trial execution", "Scientific knowledge", "Laboratory expertise", "Data sciences", "Project management", "Oncology", "Rare Disease", "ICH-GCP", "Clinical trial monitoring", "Clinical documentation", "Investigational product", "CTMS", "eTMF" ], "skillCount" : 24, "jobCategory" : "other", "jobSubcategory" : "clinical-solutions", "dataQualityScore" : 0.8888889, "_score" : 812.4827, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Life Sciences" }, { "id" : "6a305119f292fd229cefa30e", "title" : "Senior Director, Head of Site Feasibility and Enablement", "industry" : "Project Management", "salary" : { "min" : 275000.0, "max" : 425000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Senior Director, Head of Site Feasibility and Enablement in the US Biotech industry, adjusted for director-level seniority and remote work." }, "location" : "US", "locations" : [ "US" ], "timestamp" : "2026-06-16T11:49:54.975", "fingerprint" : "fa927fffb3ed4d2e579d34c5cd9956bb28b225cc79ec8a28c09a7b186d850d9a", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/d6d277dd-d47c-4112-beaf-6f858f22fcb1/apply", "externalId" : "d6d277dd-d47c-4112-beaf-6f858f22fcb1", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 12, "experienceLevel" : "Director", "technicalSkills" : "CTMS, EDC platforms, Feasibility analytics solutions", "professionalSkills" : [ "Study planning", "Study execution", "Site selection", "Enrollment forecasting", "Trial success", "Strategic partnerships", "Investigator engagement", "Patient recruitment", "Study start-up", "Process improvement", "Cross-functional governance", "Team management", "Global operations" ], "hardSkillsList" : [ "Data analytics", "Enrollment forecasting", "Site feasibility", "Study start-up strategy", "Patient recruitment strategies", "Continuous improvement initiatives" ], "softSkillsList" : [ "Leadership", "Decision-making" ], "hardSkills" : [ { "name" : "Data analytics", "level" : "intermediate" }, { "name" : "Enrollment forecasting", "level" : "intermediate" }, { "name" : "Site feasibility", "level" : "intermediate" }, { "name" : "Study start-up strategy", "level" : "intermediate" }, { "name" : "Patient recruitment strategies", "level" : "intermediate" }, { "name" : "Continuous improvement initiatives", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Decision-making" } ], "majorSkills" : "Site feasibility, Patient recruitment, Clinical operations, Team leadership", "majorSkillsList" : [ "Site feasibility", "Patient recruitment", "Clinical operations", "Team leadership" ], "coreResponsibilities" : "Define and lead regional site feasibility and enablement, Oversee feasibility assessments at country and site level, Integrate historical performance, competitive intelligence, and data analytics, Develop and maintain accurate enrollment forecasting models, Identify risks early and implement mitigation strategies, Establish and strengthen strategic partnerships with investigative sites,, Design and implement site enablement and patient recruitment, Accelerate enrollment and expand access to underserved populations, Lead continuous improvement initiatives across feasibility, study start-up,, Leverage new tools, technologies, and methodologies, Manage cross-functional governance for site selection, activation, and, Oversee and develop regional feasibility and recruitment teams, Contribute to global clinical operations initiatives, Represent regional feasibility perspectives in strategic planning and", "teamCollaboration" : "Cross-functional governance; Global teams; External partners; Matrixed environment", "projectManagementSkills" : [ "Study start-up strategy development" ], "domainKnowledge" : "Clinical development priorities; Clinical trial feasibility; Clinical trial management; Clinical operations; Patient recruitment; Investigator engagement; Global clinical development", "domainList" : [ "clinical-development-priorities", "clinical-trial-feasibility", "clinical-trial-management", "clinical-operations", "patient-recruitment", "investigator-engagement", "global-clinical-development" ], "domainSpecificKnowledge" : [ "Clinical development priorities", "Clinical trial feasibility", "Clinical trial management", "Clinical operations", "Patient recruitment", "Investigator engagement", "Global clinical development" ], "toolProficiency" : [ "Citeline", "Trialtrove" ], "communicationSkills" : "Senior stakeholder influence", "continuousLearning" : "Professional development; Continuous learning; Career growth", "innovationCreativity" : "Innovation", "problemSolvingSkills" : "Data analytics; Risk mitigation", "specialRequirements" : "Willingness to travel", "outcomesObjectives" : "Support trial success; Enhance engagement; Long-term collaboration; Accelerate enrollment; Expand access to underserved populations", "qualificationsBasic" : "Bachelor’s degree or higher in a scientific, medical, or healthcare discipline, 12+ years of experience in clinical operations, feasibility, clinical trial management, or related fields, Proven leadership experience managing feasibility, site strategy, patient recruitment, or clinical operations teams, Expertise in clinical trial feasibility, country and site selection, and study start-up strategy development, Deep understanding of patient recruitment, investigator engagement, and operational drivers of clinical trial success, Advanced analytical skills with experience interpreting complex datasets, Demonstrated ability to influence senior stakeholders, Demonstrated ability to manage cross-functional relationships in a matrixed environment, Experience working with global teams, Experience managing external partners, vendors, and CROs", "qualificationsPreferred" : "Master's degree or higher", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Define and lead the regional site feasibility and enablement strategy aligned with clinical development priorities, ensuring effective study planning and execution across the Americas. Oversee feasibility assessments at country and site level, integrating historical performance, competitive intelligence, and data analytics to inform robust site selection decisions. Develop and maintain accurate enrollment forecasting models, identifying risks early and implementing mitigation strategies to support trial success. Establish and strengthen strategic partnerships with investigative sites, site networks, and key opinion leaders to enhance engagement and long-term collaboration. Design and implement site enablement and patient recruitment strategies to accelerate enrollment and expand access to underserved populations. Lead continuous improvement initiatives across feasibility, study start-up, and recruitment processes, leveraging new tools, technologies, and methodologies. Manage cross-functional governance for site selection, activation, and enrollment execution while overseeing and developing regional feasibility and recruitment teams. Contribute to global clinical operations initiatives and represent regional feasibility perspectives in strategic planning and decision-making forums. Requirements: Bachelor’s degree or higher in a scientific, medical, or healthcare discipline, with 12+ years of experience in clinical operations, feasibility, clinical trial management, or related fields. Proven leadership experience managing feasibility, site strategy, patient recruitment, or clinical operations teams in a global or regional environment. Strong expertise in clinical trial feasibility, country and site selection, and study start-up strategy development. Deep understanding of patient recruitment, investigator engagement, and operational drivers of clinical trial success. Advanced analytical skills with experience interpreting complex datasets to inform strategic and operational decisions. Demonstrated ability to influence senior stakeholders and manage cross-functional relationships in a matrixed environment. Experience working with global teams and managing external partners, vendors, and CROs. Strong knowledge of clinical trial systems and tools such as CTMS, EDC platforms, and feasibility analytics solutions (e.g., Citeline, Trialtrove or similar). Excellent communication, leadership, and decision-making skills with a results-oriented and collaborative mindset. Willingness to travel as required to support business needs. Benefits: Competitive base salary ranging from approximately $206,200 to $276,200 annually, depending on experience, skills, and location. Eligibility for annual bonus plans or incentive compensation depending on role classification. Equity participation through discretionary stock awards and Employee Stock Purchase Plan. Comprehensive health coverage including medical, dental, and vision insurance. Retirement savings plans such as 401(k), FSA/HSA options, and financial wellness benefits. Generous paid time off and wellness-focused benefits supporting work-life balance. Opportunity to work in a global clinical development environment focused on innovation and patient impact. Strong commitment to professional development, continuous learning, and career growth. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Senior Director, Head of Site Feasibility and Enablement. Skills: Site feasibility, Patient recruitment, Clinical operations, Team leadership. Define and lead regional site feasibility and enablement. Oversee feasibility assessments at country and site level", "postedDate" : "2026-06-15T08:11:25.946", "createdAt" : "2026-06-15T08:11:25.946", "lastUpdated" : "2026-06-16T11:49:54.975", "ingestTimestamp" : "2026-06-16T03:22:18.241", "mongoId" : "6a305119f292fd229cefa30e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 275000, "salaryAnnualMax" : 425000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Data analytics", "Enrollment forecasting", "Site feasibility", "Study start-up strategy", "Patient recruitment strategies", "Continuous improvement initiatives", "Leadership", "Decision-making", "Patient recruitment", "Clinical operations", "Team leadership", "Study planning", "Study execution", "Site selection", "Trial success", "Strategic partnerships", "Investigator engagement", "Study start-up", "Process improvement", "Cross-functional governance", "Team management", "Global operations", "Study start-up strategy development", "Clinical development priorities", "Clinical trial feasibility", "Clinical trial management", "Global clinical development", "Citeline", "Trialtrove" ], "skillCount" : 29, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 806.79266, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "69cf26122beec4dd3d90b483", "title" : "Cell Therapy Specialist RN - Bone Marrow Transplant", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 86000.0, "max" : 118000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for a Cell Therapy Specialist RN in Tampa, Florida, with 3-5 years of experience, adjusted for the healthcare industry and mid-seniority level." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
Transplant (TRANSPLANT)
409 Bayshore Blvd. 4th Floor

Tampa, 33606

" ], "certifications" : [ "Active RN license", "Blood & Marrow Transplant Certified Nurse (BMTCN)", "Transplantation and Cellular Therapy Certified Nurse (TCTCN)", "Oncology Nursing Society Chemotherapy (ONS) certification", "Basic Life Support (BLS) certification", "Advanced Cardiovascular Life Support (ACLS) certification" ], "timestamp" : "2026-06-15T09:35:33.614", "fingerprint" : "c7467d73dcd429b4b59a256dd88fc0217e62cb4fc6ec858cc0b598a2081e0ee2", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=676427", "externalId" : "676427", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "experienceMinYears" : 3, "experienceMaxYears" : 5, "professionalSkills" : [ "Nursing care", "Care coordination", "Protocol development" ], "hardSkillsList" : [ "Bone marrow transplant", "Cellular therapy", "Hematology" ], "hardSkills" : [ { "name" : "Bone marrow transplant", "level" : "intermediate" }, { "name" : "Cellular therapy", "level" : "intermediate" }, { "name" : "Hematology", "level" : "intermediate" } ], "majorSkills" : "Cell Therapy, Bone Marrow Transplant, Oncology Nursing", "majorSkillsList" : [ "Cell Therapy", "Bone Marrow Transplant", "Oncology Nursing" ], "coreResponsibilities" : "Provide comprehensive nursing care, Plan and implement care, Document assessments, Identify situations requiring intervention, Develop goal-directed care plans, Safeguard patient rights, Serve as expert clinical resource, Coordinate care across continuum, Contribute to protocol development, Contribute to safety standards, Contribute to patient education", "teamCollaboration" : "Transplant teams; Oncology teams; Apheresis teams; Laboratory teams; Infusion teams; Research teams", "domainKnowledge" : "Bone Marrow Transplant; Cellular Therapy; Oncology; Hematology", "domainList" : [ "bone-marrow-transplant", "cellular-therapy", "oncology", "hematology" ], "domainSpecificKnowledge" : [ "Bone Marrow Transplant", "Cellular Therapy", "Oncology", "Hematology" ], "documentationSkills" : "Documenting assessments", "outcomesObjectives" : "Ensure optimal outcomes", "qualificationsBasic" : "Active RN license, 3–5 years clinical experience, ONS certification within 90 days, BLS certification, ACLS certification", "qualificationsPreferred" : "BMTCN within 1 year, TCTCN within 1 year", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision and in accordance with established policies, procedures, and professional standards, provides comprehensive nursing care to patients. Responsibilities include planning and implementing care, documenting assessments, identifying situations requiring intervention, and developing goal-directed care plans while safeguarding patient rights. The role aligns with Tampa General Hospital’s mission, vision, values, and quality improvement principles. As a Cell Therapy Specialist (RN), serves as an expert clinical resource, coordinates care across the continuum, and collaborates with transplant, oncology, apheresis, laboratory, infusion, and research teams. Contributes to protocol development, safety standards, and patient education initiatives to ensure optimal outcomes. Requires an Active RN license issued by Florida or a Compact State Blood & Marrow Transplant Certified Nurse (BMTCN) within 1 year of hire OR Transplantation and Cellular Therapy Certified Nurse (TCTCN) within 1 year of hire Oncology Nursing Society Chemotherapy (ONS) certification within first 90 days of hire Basic Life Support (BLS) certification Advanced Cardiovascular Life Support (ACLS) certification 3–5 years of direct clinical experience in oncology, bone marrow transplant, cellular therapy, hematology, or related specialty OR an equivalent combination of education, training, and experience Tampa", "summaryDescription" : "Cell Therapy Specialist RN - Bone Marrow Transplant at Tampa General Hospital. Skills: Cell Therapy, Bone Marrow Transplant, Oncology Nursing. Provide comprehensive nursing care. Plan and implement care", "createdAt" : "2026-06-14T02:54:28.564", "lastUpdated" : "2026-06-15T09:35:33.614", "ingestTimestamp" : "2026-06-14T02:54:28.564", "mongoId" : "69cf26122beec4dd3d90b483", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 86000, "salaryAnnualMax" : 118000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Bone marrow transplant", "Cellular therapy", "Hematology", "Cell Therapy", "Bone Marrow Transplant", "Oncology Nursing", "Nursing care", "Care coordination", "Protocol development", "Cellular Therapy", "Oncology", "Active RN license", "Blood & Marrow Transplant Certified Nurse (BMTCN)", "Transplantation and Cellular Therapy Certified Nurse (TCTCN)", "Oncology Nursing Society Chemotherapy (ONS) certification", "Basic Life Support (BLS) certification", "Advanced Cardiovascular Life Support (ACLS) certification" ], "skillCount" : 17, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 792.144, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "69dde45b2beec4dd3d9a3f29", "title" : "Budget Administrator - Clinical Trials", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 89806.0, "max" : 139198.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "US-Nationwide-USA-Remote-US-Remote", "locations" : [ "US-Nationwide-USA-Remote-US-Remote", "Clinical Research", "Remote, Days, Days" ], "timestamp" : "2026-06-15T09:44:57.962", "fingerprint" : "787641335173ccfcf78ecc1c91956fec014c8027f6cc7ccaef7f86c151172420", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=227144", "externalId" : "227144", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 3, "professionalSkills" : [ "Research administration", "Contract negotiation" ], "hardSkillsList" : [ "Budget development", "Coverage analysis", "Cost allocation", "Financial data entry", "Financial data review", "Pricing precedent", "Costing analysis" ], "hardSkills" : [ { "name" : "Budget development", "level" : "intermediate" }, { "name" : "Coverage analysis", "level" : "intermediate" }, { "name" : "Cost allocation", "level" : "intermediate" }, { "name" : "Financial data entry", "level" : "intermediate" }, { "name" : "Financial data review", "level" : "intermediate" }, { "name" : "Pricing precedent", "level" : "intermediate" }, { "name" : "Costing analysis", "level" : "intermediate" } ], "majorSkills" : "Clinical trial budgets, Coverage analysis, Financial data management", "majorSkillsList" : [ "Clinical trial budgets", "Coverage analysis", "Financial data management" ], "coreResponsibilities" : "Coordinate coverage analyses and budgets, Develop coverage analyses and budgets, Liaise between sponsors and COH departments, Determine suitable coverage justifications, Determine cost allocations, Finalize clinical trial budgets, Obtain approval of coverage analyses, Obtain approval of budget estimates, Obtain approval of detailed budgets, Negotiate budgets with clinical trial sponsors, Track data and enter financial data, Maintain financial data, Review financial data, Enter financial data into OnCore, Maintain financial data in OnCore, Review financial data in OnCore, Initiate sign-off process, Review protocol amendments, Perform critical assessment projects, Confirm funding source, Assure negotiations are consistent, Perform detailed analyses, Establish precedent pricing, Develop better drafting techniques, Develop better development techniques, Assess comparable nature of projects, Ensure appropriate costing, Analyze new protocols, Analyze letters of intent, Analyze synopses, Determine coverage analysis necessity, Determine budget necessity, Determine prioritization", "teamCollaboration" : "Liaise between external sponsors; Works with Principal Investigators; Works with study teams; Coordinate with all relevant groups", "domainKnowledge" : "Clinical trials; HCPCS / CPT codes; Standard of care; Medicare regulations; Medical terminology; Oncology clinical trials", "domainList" : [ "clinical-trials", "hcpcs-cpt-codes", "standard-of-care", "medicare-regulations", "medical-terminology", "oncology-clinical-trials" ], "domainSpecificKnowledge" : [ "Clinical trials", "HCPCS / CPT codes", "Standard of care", "Medicare regulations", "Medical terminology", "Oncology clinical trials" ], "documentationSkills" : "Coverage justifications", "problemSolvingSkills" : "Critical assessment projects", "qualificationsBasic" : "Bachelor's Degree or equivalent, Three years of related budget experience, Working knowledge of clinical trials, Familiarity with HCPCS / CPT codes, Understanding of standard of care, Familiarity with Medicare regulations, Working knowledge of medical terminology", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. Position Summary: Coordinates and develops coverage analyses and budgets for both industry sponsored and non-industry sponsored clinical trials, along with any corresponding amendments. Liaises between external sponsors and COH departments to determine suitable coverage justifications and cost allocations for unique clinical trial procedures. Works with Principal Investigators and study teams to finalize clinical trial budgets and obtain approval of coverage analyses, budget estimates, and/or detailed budgets. Negotiates budgets with clinical trial sponsors to ensure optimal cost efficiency. Tracks data and enters, maintains, and reviews financial data from finalized clinical trial agreements and budgets into the OnCore Clinical Trial Management System (CTMS). As a successful candidate, you will: Coordinate with all relevant groups to draft, finalize and gain approval of coverage analyses and budgets while tracking all appropriate data metrics. This includes documenting qualifying clinical trial status, researching coverage limitations, verifying expected medical necessity, and assigning costs for clinical and non-clinical components of each trial. Must understand the clinical trial and corresponding protocol in order to determine coding and charge determinations. Enter and/or review financial data in OnCore and initiate the sign-off process of the OnCore calendar/financial console. Review protocol amendments for any revisions affecting the coverage analysis and/or budget; update previously documented information. Perform critical assessment projects to confirm funding source and assure that negotiations will be consistent with institutional guidelines. Perform detailed analyses of current coverage analyses or budgets to establish precedent pricing and better drafting and development techniques. Assess comparable nature of projects by factors such as study phase or disease-type to ensure appropriate costing. Analyze new protocols, letters of intent, synopses, etc., received from sponsors, review committees or PI/study teams to determine coverage analysis/budget necessity and/or prioritization in coordination with department leadership. Your qualifications should include: Bachelor’s Degree or equivalent combination of education and experience. Three years of related budget experience working in research administration, a Contract Research Organization, pharma or biotech industry, a medical or clinical practice arena, or health insurance industry. Working knowledge of clinical trials. Familiarity with HCPCS / CPT codes. Understanding of what is standard of care or routine care and what is considered research-related in the context of clinical trials. Familiarity with Medicare regulations, guidelines, policies. Working knowledge of medical terminology specific to oncology clinical trials and general study budgeting techniques and coverage analysis techniques. Additional information: City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. Job Status: Full time, exempt Salary range $ 89,806 - $139,198 City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here . To learn more about our Comprehensive Benefits, please CLICK HERE . US-Nationwide-USA-Remote-US-Remote", "summaryDescription" : "Budget Administrator - Clinical Trials at City of Hope. Skills: Clinical trial budgets, Coverage analysis, Financial data management. Coordinate coverage analyses and budgets. Develop coverage analyses and budgets", "createdAt" : "2026-06-14T08:36:18.783", "lastUpdated" : "2026-06-15T09:44:57.962", "ingestTimestamp" : "2026-06-14T08:36:18.783", "mongoId" : "69dde45b2beec4dd3d9a3f29", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 89806, "salaryAnnualMax" : 139198, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Budget development", "Coverage analysis", "Cost allocation", "Financial data entry", "Financial data review", "Pricing precedent", "Costing analysis", "Clinical trial budgets", "Financial data management", "Research administration", "Contract negotiation", "Clinical trials", "HCPCS / CPT codes", "Standard of care", "Medicare regulations", "Medical terminology", "Oncology clinical trials" ], "skillCount" : 17, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 787.59906, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a308767f292fd229c088975", "title" : "Patient Cell Operations Manager - Contract", "company" : "Lyell Immunopharma", "industry" : "Biotech", "salary" : { "min" : 85.0, "max" : 95.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Bothell, Washington, United States", "locations" : [ "Bothell", "Washington", "United States", "Seattle", "Washington", "United States" ], "timestamp" : "2026-06-16T13:09:54.563", "fingerprint" : "4ba5507d40b368ff601fc7ea820ebad64379c636667da8f36bc41db77bbe75b4", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/lyellimmunopharma/jobs/7773784003", "externalId" : "7773784003", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bothell", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.7623204,-122.2054035" } ], "locationText" : "Bothell, Washington, United States", "employmentType" : "CONTRACT", "experienceLevel" : "Manager", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Patient cell handling", "Apheresis collection", "Drug product handling", "CAPA management", "Deviation management", "Material validation", "Shipping container validation" ], "softSkillsList" : [ "Forward-thinking leadership" ], "hardSkills" : [ { "name" : "Patient cell handling", "level" : "intermediate" }, { "name" : "Apheresis collection", "level" : "intermediate" }, { "name" : "Drug product handling", "level" : "intermediate" }, { "name" : "CAPA management", "level" : "intermediate" }, { "name" : "Deviation management", "level" : "intermediate" }, { "name" : "Material validation", "level" : "intermediate" }, { "name" : "Shipping container validation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Forward-thinking leadership" } ], "majorSkills" : "Patient Cell Operations, Supply Chain, Cross-functional collaboration", "majorSkillsList" : [ "Patient Cell Operations", "Supply Chain", "Cross-functional collaboration" ], "coreResponsibilities" : "Manage patient cell operations, Lead day-to-day operational management, Manage apheresis, tissue collection, and drug product handling, Coordinate day-to-day processes, Execute, manage, and drive work, Create controlled manuals for apheresis collection, Create controlled manuals for drug product administration, Drive right-first-time apheresis collection, Drive right-first-time drug product handling, Manage day-to-day relationships with apheresis suppliers, Manage CAPAs related to improper cell handling, Manage deviations related to improper cell handling, Partner with Manufacturing, Partner with Quality, Partner with Clinical Operations, Partner with external vendors, Partner with service providers, Ensure materials are validated, Ensure shipping containers are validated, Establish electronic tools, Establish processes for Patient Cell Operations, Establish procedures for Patient Cell Operations, Improve electronic tools, Improve processes for Patient Cell Operations, Improve procedures for Patient Cell Operations", "teamCollaboration" : "Cross-functional teams; External clinical sites; Apheresis centers", "domainKnowledge" : "Cell therapy lifecycle; Hematologic malignancies; Solid tumors; CAR T-cell therapies; T-cell biology; Tumor cytotoxicity", "domainList" : [ "cell-therapy-lifecycle", "hematologic-malignancies", "solid-tumors", "car-t-cell-therapies", "t-cell-biology", "tumor-cytotoxicity" ], "domainSpecificKnowledge" : [ "Cell therapy lifecycle", "Hematologic malignancies", "Solid tumors", "CAR T-cell therapies", "T-cell biology", "Tumor cytotoxicity" ], "documentationSkills" : "Controlled manuals", "innovationCreativity" : "Establish scalable processes; Establish procedures; Establish training frameworks", "outcomesObjectives" : "Deliver right-first-time execution; Support manufacturing success; Support clinical trial success", "qualificationsBasic" : "7 years experience", "qualificationsPreferred" : "5 years management experience, Management experience in patient cell operations", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Using living cells to treat – and sometimes even cure – cancer is one of the most dramatic advances in modern medicine. Patients with hematologic malignancies have been successfully treated with cell therapies. However, these profound results have not yet been achieved in patients with solid tumors, representing approximately 90% of all cancers. And for patients with hematologic malignancies, there is a need for next-generation cell therapies that can deliver increased response rates and longer duration of response. We are a clinical-stage company advancing a pipeline of next-generation CAR T-cell therapies for patients with solid tumors or hematologic malignancies. Lyell’s product candidates are enhanced with novel technology designed to generate T cells that resist exhaustion and have qualities of durable stemness in order to drive durable tumor cytotoxicity and achieve consistent and long-lasting clinical response. We were founded by cell therapy pioneers whose decades of research elevated the broader understanding of T-cell biology and its interaction with cancer. In our quest to advance next-generation CAR T-cell therapies, we have built a fully integrated company capable of discovering new technologies, translating science into therapies, manufacturing cell therapy products, and clinically evaluating them in patients. Our culture is based on Science, Respect, Collaboration, and Courage and reflects who we are, the environment we create, and our mission's urgency. Position Summary Lyell is seeking an experienced contractor to perform the Patient Cell Operations management function within the Supply Chain organization, reporting to the Supply Chain leadership. The contractor will lead the day-to-day operational management of patient cells across the cell-therapy lifecycle, including apheresis, tissue collection, and final drug product handling. This is a highly cross-functional role that works closely with Manufacturing, Clinical Operations, Quality, and external clinical sites and apheresis centers to deliver right-first-time execution of patient cell handling processes that support manufacturing and clinical trial success. As a contractor, the individual will run and coordinate these processes day-to-day. The individual executes, manages, and drives the work under the direction of the Supply Chain leadership, escalating decisions when required. To be successful, the individual must be self-motivated, detail-oriented, and able to operate effectively in a dynamic environment, bringing forward-thinking leadership to help establish scalable processes, procedures, and training frameworks that support the growth of the Patient Cell Operations team. Key Responsibilities Patient Cell Operations Execution Create, manage, and maintain controlled manuals describing processes for apheresis collection and final drug product administration. Drive right-first-time apheresis and final drug product handling at clinical sites and apheresis centers. Manage day-to-day relationships with Lyell healthy donor apheresis suppliers. Manage CAPAs and deviations related to improper handling of patient cells, partnering with Lyell process owners for final disposition and approval. Partner cross-functionally with Manufacturing, Quality, Clinical Operations, and external vendors and service providers. Ensure materials and shipping containers required for patient cell collection, transport, and final drug product handling are properly validated. Establish and continuously improve electronic tools, processes, and procedures that support Patient Cell Operations activities. Clinical Site Readiness or MBA or MSc with a minimum of 7 years’ experience PREFERRED EXPERIENCE: At least 5 years management experience in patient cell operations Engagement Details This is a contract position. Compensation is commensurate with experience and will be discussed during the interview process. Contract duration: 4-6 months. Schedule: full-time (40 hours/week). The hourly rate of pay is between $85.00 - 95.00 per hour", "summaryDescription" : "Patient Cell Operations Manager - Contract at Lyell Immunopharma. Skills: Patient Cell Operations, Supply Chain, Cross-functional collaboration. Manage patient cell operations. 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Tel Aviv, Israel; United States", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "CTMS, EDC, eTMF, Risk-based monitoring", "professionalSkills" : [ "Clinical trial management", "Operational planning", "Regulatory standards", "GCP compliance", "SOP compliance", "Protocol development", "CRF design", "ICF review", "Operational study plans", "Data collection", "Database lock", "Regulatory filings", "Inspection readiness", "Audit preparation" ], "hardSkillsList" : [ "Clinical operations", "Global clinical trials", "Immunology indications", "Autoimmune diseases", "Inflammatory diseases", "Biologics", "Monoclonal antibodies", "Advanced therapies", "Clinical trial regulations", "Operational best practices", "Pivotal trials" ], "softSkillsList" : [ "Leadership", "Problem-solving" ], "hardSkills" : [ { "name" : "Clinical operations", "level" : "intermediate" }, { "name" : "Global clinical trials", "level" : "intermediate" }, { "name" : "Immunology indications", "level" : "intermediate" }, { "name" : "Autoimmune diseases", "level" : "intermediate" }, { "name" : "Inflammatory diseases", "level" : "intermediate" }, { "name" : "Biologics", "level" : "intermediate" }, { "name" : "Monoclonal antibodies", "level" : "intermediate" }, { "name" : "Advanced therapies", "level" : "intermediate" }, { "name" : "Clinical trial regulations", "level" : "intermediate" }, { "name" : "Operational best practices", "level" : "intermediate" }, { "name" : "Pivotal trials", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Problem-solving" } ], "majorSkills" : "Clinical trial management, Immunology, Autoimmune diseases", "majorSkillsList" : [ "Clinical trial management", "Immunology", "Autoimmune diseases" ], "coreResponsibilities" : "Lead operational strategy, Plan clinical trials, Execute clinical trials, Oversee clinical trials, Serve as primary operational point of contact, Oversee selection of CROs, Manage CROs, Oversee vendor selection, Manage vendors, Drive site feasibility, Drive site selection, Drive site activation, Drive patient recruitment strategies, Manage ongoing site management, Develop study timelines, Maintain study timelines, Develop risk mitigation strategies, Maintain risk mitigation strategies, Develop operational tracking tools, Maintain operational tracking tools, Collaborate on protocol development, Collaborate on CRF design, Collaborate on ICF review, Collaborate on operational study plans, Ensure studies compliance, Identify operational issues, Resolve operational issues, Escalate risks, Implement mitigation strategies, Oversee data collection activities, Oversee database lock readiness, Support data review processes, Contribute to regulatory filings, Contribute to inspection readiness, Contribute to audit preparation, Provide leadership to team members, Provide mentorship to team members, Contribute to process improvement initiatives", "teamCollaboration" : "Internal cross-functional teams; External partners; CROs; Vendors; Sites; Clinical Operations team members", "projectManagementSkills" : [ "Clinical trial management", "Risk mitigation", "Timeline management" ], "domainKnowledge" : "Immunology; Autoimmune diseases; Inflammatory diseases; Biologics; Monoclonal antibodies; Advanced therapies; GCP; ICH guidelines; Clinical trial regulations", "domainList" : [ "immunology", "autoimmune-diseases", "inflammatory-diseases", "biologics", "monoclonal-antibodies", "advanced-therapies", "gcp", "ich-guidelines", "clinical-trial-regulations" ], "domainSpecificKnowledge" : [ "Immunology", "Autoimmune diseases", "Inflammatory diseases", "Biologics", "Monoclonal antibodies", "Advanced therapies", "GCP", "ICH guidelines", "Clinical trial regulations" ], "toolProficiency" : [ "CTMS", "EDC", "eTMF", "Risk-based monitoring tools" ], "documentationSkills" : "Protocol development; CRF design; ICF review; Operational study plans; Regulatory filings", "problemSolvingSkills" : "Problem-solving; Risk mitigation; Issue resolution", "specialRequirements" : "Travel up to 20%, Domestic travel, International travel, Overnight stays, Availability during Eastern Time", "outcomesObjectives" : "Ensure studies delivered on time; Ensure studies within scope; Ensure studies compliance; Achieve enrollment goals", "qualificationsBasic" : "Bachelor's degree in life sciences, Minimum 5 years of experience in clinical operations, At least 3 years in a Senior CTM role, Proven track record of managing global clinical trials, Experience with biologics, Knowledge of GCP/ICH guidelines, Experience in early- to late-stage development programs", "qualificationsPreferred" : "Advanced degree preferred, Experience in rare autoimmune indications, Familiarity with adaptive trial designs, Experience with complex biomarker-driven studies", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully. Job Summary: The Senior Clinical Trial Manager (Sr. CTM) will lead the operational planning, execution, and oversight of complex, global clinical studies in the field of immunology and autoimmune diseases. This role is responsible for ensuring studies are delivered on time, within scope, and in compliance with regulatory standards, Good Clinical Practice (GCP), and company Standard Operating Procedures (SOPs). The Sr. CTM will partner closely with internal cross-functional teams (Clinical Development, Regulatory, Biometrics, Safety, and Quality) and external partners (CROs, vendors, and sites) to ensure operational excellence. This individual will also play a critical role in driving strategic decision-making and supporting inspection readiness and regulatory submissions. Work Arrangement the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company's discretion based on business need. Essential Duties and Responsibilities: Lead the operational strategy, planning, and execution of global Phase 1–4 clinical trials in immunology indications (e.g., autoimmune and inflammatory diseases). Serve as the primary operational point of contact for internal stakeholders and external partners. Oversee the selection and management of CROs and other vendors, including scope of work, budget development, contracting, and performance oversight. Drive site feasibility, site selection, activation, patient recruitment strategies, and ongoing site management to ensure achievement of enrollment goals. Develop and maintain study timelines, risk mitigation strategies, and operational tracking tools. Collaborate with cross-functional teams on protocol development, CRF design, ICF review, and development of operational study plans. Ensure studies are conducted in compliance with GCP/ICH guidelines, local regulatory requirements, and internal SOPs. Proactively identify and resolve operational issues, escalating risks and implementing mitigation strategies as needed. Oversee data collection activities, database lock readiness, and support data review processes. Contribute to regulatory filings, inspection readiness, and audit preparation. Provide leadership and mentorship to Clinical Operations team members. Contribute to process improvement initiatives within Clinical Operations to enhance efficiency and quality. Perform other duties and responsibilities as assigned Qualifications: Education: Bachelor’s degree in life sciences or related field (advanced degree preferred) Minimum 5 years of experience in clinical operations in the biopharmaceutical industry, with at least 3 years in a Senior CTM or equivalent leadership role. Proven track record of managing global, multi-center clinical trials in immunology or autoimmune disease indications. Experience with biologics, monoclonal antibodies, or advanced therapies. Strong knowledge of GCP/ICH guidelines, clinical trial regulations, and operational best practices. Experience in rare autoimmune indications or immune-mediated inflammatory diseases. Familiarity with adaptive trial designs or complex biomarker-driven studies. Experience in early- to late-stage development programs, including pivotal trials. Proficiency with electronic systems such as CTMS, EDC, eTMF, and risk-based monitoring tools. Ability to thrive in a fast-paced, dynamic environment and work independently with minimal supervision Excellent communication, leadership, and problem-solving skills. This position requires availability during Eastern Time (ET) business hours This role may require domestic and international travel, including overnight stays, up to 20% or more based on business needs Salary Range: The expected annual salary range for this position is listed below. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance. Salary Range $178,000—$194,500 USD Benefits: We offer a comprehensive benefits package including: Medical, Dental & Vision insurance (employee premiums 100% covered by company) 20 accrued days combined time off (PTO/Sick), 12 company holidays, & winter recharge Flexible work arrangements / hybrid schedule Health Savings Account (HSA) *Benefits are subject to eligibility requirements and plan terms. Additional details provided during the offer process* Equal Employment Opportunity: Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. Reasonable Accommodation: If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates. Privacy Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at Privacy Policy - Beeline Medicines", "summaryDescription" : "Senior Clinical Trial Manager (Atopic Dermatitis) at Beeline Medicines. Skills: Clinical trial management, Immunology, Autoimmune diseases. Lead operational strategy. Plan clinical trials", "postedDate" : "2026-06-12T22:01:31.594", "createdAt" : "2026-06-12T22:01:31.594", "lastUpdated" : "2026-06-14T22:32:57.002", "ingestTimestamp" : "2026-06-12T22:01:31.594", "mongoId" : "6a2c5e6674d8ee00a08e3c39", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 155000, "salaryAnnualMax" : 210000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Clinical operations", "Global clinical trials", "Immunology indications", "Autoimmune diseases", "Inflammatory diseases", "Biologics", "Monoclonal antibodies", "Advanced therapies", "Clinical trial regulations", "Operational best practices", "Pivotal trials", "Leadership", "Problem-solving", "Clinical trial management", "Immunology", "Operational planning", "Regulatory standards", "GCP compliance", "SOP compliance", "Protocol development", "CRF design", "ICF review", "Operational study plans", "Data collection", "Database lock", "Regulatory filings", "Inspection readiness", "Audit preparation", "Risk mitigation", "Timeline management", "GCP", "ICH guidelines", "CTMS", "EDC", "eTMF", "Risk-based monitoring tools" ], "skillCount" : 36, "jobCategory" : "operations", "jobSubcategory" : "clinical-operations", "dataQualityScore" : 0.8888889, "_score" : 779.16864, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a2c7ae874d8ee00a09475c2", "title" : "Production Manager, Cell Manufacturing", "company" : "Gotion, Inc.", "salary" : { "min" : 115000.0, "max" : 165000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Production Manager in Cell Manufacturing in Manteno, IL, adjusted for manager seniority and the manufacturing industry." }, "location" : "Manteno, Illinois, United States", "locations" : [ "Manteno", "Illinois", "United States" ], "timestamp" : "2026-06-16T01:47:48.396", "fingerprint" : "82482a05fc0e20d63e2c0281f3a2e78120386136b488684c333284f702d274a5", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/gotion/jobs/8399218002", "externalId" : "8399218002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Manteno", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.2501677,-87.8326423" } ], "locationText" : "Manteno, Illinois, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "remoteFriendly" : false, "rawDescription" : "Gotion Inc. is based in Silicon Valley, CA, currently building a Manufacturing facility in Manteno, IL and has R&D centers in Ohio, China, Japan and Europe. We innovate in the next generation electric vehicle and energy storage technologies (lithium batteries and related systems) with the aim to accelerate electrified transportation and achieve sustainable development. Gotion is powered by a leading power battery technology company that provides solutions for vehicles including the world's first mass commercial e-bus route. Gotion is a career destination - we are not simply attempting to just fill another job, but to pursue a dream of global green energy together! We offer outstanding opportunities to individuals seeking an exciting and challenging working environment. Everyone is highly valued and plays a vital role in the growth of our organization. Job Summary: Gotion Inc., a leading innovator in battery cell manufacturing, is seeking an experienced and results-oriented Cell Production Manager to oversee our production operations in Manteno, IL. The ideal candidate will leverage their expertise in manufacturing production management to drive operational excellence, ensure product quality, and achieve production goals. This role requires strong leadership, technical knowledge, and a commitment to safety and efficiency. Key Responsibilities: Production & Shop-floor Management: Develop and implement production plans to meet deadlines and production targets. Monitor and manage production progress, quality metrics, and costs to improve overall efficiency. Implement and maintain 5S standards and Visual Management systems to ensure a clean, organized, and transparent work environment. Conduct daily Gemba walks to identify and resolve floor-level bottlenecks in real-time. Optimize workflows through lean manufacturing practices and reduce production waste. Equipment and Process Oversight: Oversee the maintenance and operation of production equipment to ensure consistent performance. Drive continuous improvement initiatives and implement smart manufacturing techniques where applicable. Team Leadership: Build, train, and manage a high-performing production team. Evaluate team performance regularly and foster a collaborative work environment. Manage labor relations and conflict resolution effectively within a diverse workforce Collaboration and Coordination: Collaborate with R&D, Quality, and Procurement teams to support new product launches and stabilize production processes. Ensure compliance with ISO9001, ISO14001, and other quality management standards. Safety and Reporting: Enforce safety regulations to maintain a safe working environment. Prepare detailed production reports, analyze data, and provide actionable insights to management. Qualifications: Education & Background: Bachelor’s degree or above in Industrial Engineering, Mechanical Engineering, Automation, or related fields. Work Experience: Minimum 5 years of experience in manufacturing production management. At least 3 years in a managerial role, preferably in large-scale production environments. Hands-on experience with lean manufacturing, Six Sigma, or similar methodologies is preferred. Technical Skills: Comprehensive understanding of manufacturing processes, production techniques, and equipment management. Strong capabilities in production planning, cost control, quality assurance, and efficiency improvement. Familiarity with ERP systems and production management software (e.g., SAP, MES) Soft Skills: Exceptional leadership, communication, and team management abilities. Analytical mindset with the ability to make data-driven decisions. High level of responsibility and resilience in a fast-paced environment. Resilience and the ability to lead a team through high-pressure production ramps and process stabilization. The U. S. base salary range for this full-time position is $100,000.00 - $150,000.00, plus eligibility for bonus and benefits. Our salary ranges are determined by factors such as the role, level, and geographic location. The range listed in the job posting represents the minimum and maximum target salaries for this position across all U. S. locations. Actual compensation within the range will be influenced by the specific work location, along with factors such as job-related skills, experience, and relevant education or training. Your recruiter will provide more details about the specific salary range for your preferred location during the hiring process. Please note that the listed compensation reflects the base salary only and does not include bonus or benefits. Gotion Inc. is proud to be an equal opportunity employer. We are dedicated to fostering a diverse workforce that reflects the communities we serve, cultivating a culture of inclusion and belonging, and ensuring equal employment opportunities for all. We provide equal opportunity to all individuals regardless of race, creed, color, religion, gender, sexual orientation, gender identity or expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related conditions (including breastfeeding), parental status, criminal histories consistent with legal requirements, or any other characteristic protected by law. At Gotion Inc., we strive to create an environment where everyone feels valued, respected, and empowered to thrive.", "summaryDescription" : "Production Manager, Cell Manufacturing at Gotion, Inc.", "postedDate" : "2026-06-14T19:11:44.934", "createdAt" : "2026-06-14T19:11:44.934", "lastUpdated" : "2026-06-16T01:47:48.396", "ingestTimestamp" : "2026-06-14T19:11:44.934", "mongoId" : "6a2c7ae874d8ee00a09475c2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 115000, "salaryAnnualMax" : 165000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 0.8888889, "_score" : 771.3582, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.98 }, { "id" : "69dde45b2beec4dd3d9a3f15", "title" : "Sr Clinical Trials Data Coord", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 85000.0, "max" : 125000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline adjusted for seniority, industry, and location in Duarte, CA." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Clinical Research", "Remote, Days, Days" ], "certifications" : [ "Good Clinical Practice (GCP) training", "Human Subjects Protection (HSP) training", "SOCRA certification", "ACRP certification" ], "timestamp" : "2026-06-15T09:54:10.735", "fingerprint" : "dd7dfdd6053cedd7799f16b5572f499ebba8357ae97ad929a6a6be793f1d32ce", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=231165", "externalId" : "231165", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1394513,-117.9772873" } ], "locationText" : "Duarte, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 7, "experienceLevel" : "Senior", "technicalSkills" : "SQL, Python, R, Scala, Spark, Dbt, Snowflake, BigQuery, Redshift, Databricks, Fivetran, Airflow, Dbt Cloud, Delta Lake, Scikit-learn, TensorFlow, PyTorch, XGBoost, LightGBM, Hugging Face, MLflow, AWS, GCP, Azure", "professionalSkills" : [ "Data collection", "Data entry", "Quality assurance", "Query resolution", "Data reporting", "Study monitoring", "Regulatory compliance", "Data management", "Workflow development", "Peer data reviews", "Training research staff" ], "hardSkillsList" : [ "Clinical trial data", "Research protocols", "Medical records review", "Data discrepancies", "Study visits", "Financial triggers", "Adverse event data", "Data quality checks", "Data cleaning", "SAE follow-up", "Study calendars", "Data completion 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"name" : "Inspection readiness", "level" : "intermediate" }, { "name" : "EDC builds", "level" : "intermediate" }, { "name" : "Data standards", "level" : "intermediate" }, { "name" : "Process improvement", "level" : "intermediate" } ], "majorSkills" : "Clinical trials, Data management, Regulatory compliance", "majorSkillsList" : [ "Clinical trials", "Data management", "Regulatory compliance" ], "coreResponsibilities" : "Enter clinical trial data, Manage clinical trial data, Ensure data accuracy, Ensure data completeness, Ensure data compliance, Resolve queries, Maintain regulatory compliance, Collaborate with sponsors, Collaborate with physicians, Collaborate with clinical coordinators, Resolve protocol issues, Resolve data discrepancies, Ensure proper documentation, Manage adverse event documentation, Classify adverse events, Follow up on SAEs, Maintain study calendars, Maintain financial triggers, Track data completion, Support monitoring visits, Support study initiation visits, Support audits, Support inspection readiness, Assist with EDC builds, Create data standards, Prepare reports, Participate in CAPA, Participate in process improvement, Mentor peers", "teamCollaboration" : "Working closely with physicians; Working closely with clinical coordinators; Working closely with research teams", "domainKnowledge" : "Oncology clinical trials; First-in-Human studies; Phase IV studies; FDA guidelines; ICH-GCP; ALCOA+; HIPAA; MedDRA; CTCAE; WHO-DDE", "domainList" : [ "oncology-clinical-trials", "first-in-human-studies", "phase-iv-studies", "fda-guidelines", "ich-gcp", "alcoa", "hipaa", "meddra", "ctcae", "who-dde" ], "domainSpecificKnowledge" : [ "Oncology clinical trials", "First-in-Human studies", "Phase IV studies", "FDA guidelines", "ICH-GCP", "ALCOA+", "HIPAA", "MedDRA", "CTCAE", "WHO-DDE" ], "toolProficiency" : [ "CTMS", "EMR", "OnCore", "EDC" ], "documentationSkills" : "Clinical documentation; Data management plans", "problemSolvingSkills" : "Data quality; Data accuracy; Data completeness; Data compliance", "qualificationsBasic" : "Bachelor's degree in Science, 5-7 years clinical research experience, GCP training within 1 month, HSP training within 1 month", "qualificationsPreferred" : "Ability to obtain SOCRA certification, Ability to obtain ACRP certification", "remoteFriendly" : false, "rawDescription" : "Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. The Senior Clinical Trials Data Coordinator supports complex oncology clinical trials from First-in-Human and Phase I through Phase IV by coordinating data collection, entry, quality assurance, and query resolution to ensure accurate, reliable, and compliant research data. The role involves interpreting research protocols, reviewing medical records, resolving discrepancies, and maintaining study visits and financial triggers within the Clinical Trial Management System (CTMS) aligned with Electronic Data Capture (EDC) systems. Working closely with physicians, clinical coordinators, and research teams, the coordinator ensures timely data reporting, supports adverse event data collection, and contributes to study monitoring and regulatory compliance. Additionally, the role includes performing peer data reviews, assisting in the development of data management plans and workflows, and providing training and guidance to research data staff to maintain high-quality clinical trial data and efficient research operations. As a successful candidate, you will: Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. Ensure data accuracy, completeness, and compliance through quality checks, data cleaning, and timely resolution of queries. Maintain regulatory compliance with FDA, ICH-GCP, ALCOA+, HIPAA, and other applicable guidelines for clinical research data management. Collaborate with sponsors, physicians, and clinical coordinators to resolve protocol issues, data discrepancies, and ensure proper documentation. Manage adverse event documentation and classification using standard dictionaries such as MedDRA, CTCAE, and WHO-DDE, including SAE follow-up and query resolution. Maintain study calendars, financial triggers, and data completion tracking in CTMS to support billing and study financial management. Support monitoring visits, study initiation visits, audits, and inspection readiness, ensuring data quality and completeness. Contribute to data management improvements by assisting with EDC builds, creating data standards, preparing reports, participating in CAPA and process improvement initiatives, and mentoring peers. Your qualifications should include: Minimum Education Bachelor’s degree in Science, Health, or a related field from an accredited university, or equivalent relevant work experience. Minimum Experience : Minimum of 5–7 years of clinical research or related experience. Required Certifications: Completion of Good Clinical Practice (GCP) training within 1 month of employment. Completion of Human Subjects Protection (HSP) training within 1 month of employment. Ability to obtain SOCRA or ACRP certification within 2 years of employment. Systems Knowledge: Experience with Clinical Trial Management Systems (CTMS), Electronic Medical Records (EMR), and eRegulatory systems. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here . To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Sr Clinical Trials Data Coord at City of Hope. Skills: Clinical trials, Data management, Regulatory compliance. Enter clinical trial data. Manage clinical trial data", "createdAt" : "2026-06-14T07:25:53.208", "lastUpdated" : "2026-06-15T09:54:10.735", "ingestTimestamp" : "2026-06-14T07:25:53.208", "mongoId" : "69dde45b2beec4dd3d9a3f15", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 85000, "salaryAnnualMax" : 125000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Clinical trial data", "Research protocols", "Medical records review", "Data discrepancies", "Study visits", "Financial triggers", "Adverse event data", "Data quality checks", "Data cleaning", "SAE follow-up", "Study calendars", "Data completion tracking", "Billing management", "Audit readiness", "Inspection readiness", "EDC builds", "Data standards", "Process improvement", "Clinical trials", "Data management", "Regulatory compliance", "Data collection", "Data entry", "Quality assurance", "Query resolution", "Data reporting", "Study monitoring", "Workflow development", "Peer data reviews", "Training research staff", "Oncology clinical trials", "First-in-Human studies", "Phase IV studies", "FDA guidelines", "ICH-GCP", "ALCOA+", "HIPAA", "MedDRA", "CTCAE", "WHO-DDE", "Good Clinical Practice (GCP) training", "Human Subjects Protection (HSP) training", "SOCRA certification", "ACRP certification", "CTMS", "EMR", "OnCore", "EDC" ], "skillCount" : 48, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "_score" : 762.5827, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c7ae874d8ee00a09475f2", "title" : "Technical Program Manager, Cell Product", "company" : "Gotion, Inc.", "industry" : "Manufacturing", "salary" : { "min" : 100000.0, "max" : 200000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Fremont, California, United States", "locations" : [ "Fremont", "California", "United States" ], "timestamp" : "2026-06-15T07:22:56.222", "fingerprint" : "a4966e7380e18f40897f2586e48ddf84c191d285a97a6a2bb480eeed57521b1e", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/gotion/jobs/7049534002", "externalId" : "7049534002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Fremont", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.5482697,-121.9885710" } ], "locationText" : "Fremont, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Master's", "experienceMinYears" : 5, "experienceLevel" : "Manager", "technicalSkills" : "Cell product development, Manufacturing program plans", "professionalSkills" : [ "Project management", "Cross-functional team management" ], "hardSkillsList" : [ "Battery cell technology" ], "hardSkills" : [ { "name" : "Battery cell technology", "level" : "intermediate" } ], "majorSkills" : "Cell product development, Project management", "majorSkillsList" : [ "Cell product development", "Project management" ], "coreResponsibilities" : "Engage with US OEM customers, Drive cell development, Coordinate cell manufacturing, Manage projects from conception, Develop manufacturing program plans, Define strategy, scope, schedule, Align manufacturing program, Create project schedules, Communicate project schedules, Identify innovative solutions, Overcome project obstacles, Prioritize cross-functional tasks, Track cross-functional tasks", "teamCollaboration" : "Cross-functional teams; Headquarter cell team", "projectManagementSkills" : [ "Program planning", "Schedule adherence", "Resource balancing" ], "domainKnowledge" : "Lithium-ion battery cell technology; Electric vehicle technology; Energy storage technologies", "domainList" : [ "lithium-ion-battery-cell-technology", "electric-vehicle-technology", "energy-storage-technologies" ], "domainSpecificKnowledge" : [ "Lithium-ion battery cell technology", "Electric vehicle technology", "Energy storage technologies" ], "toolProficiency" : [ "JIRA", "Microsoft Project", "Confluence" ], "communicationSkills" : "Communicate project schedules", "documentationSkills" : "Manufacturing program plans", "innovationCreativity" : "Innovative solutions", "problemSolvingSkills" : "Overcome project obstacles", "specialRequirements" : "Travel as required", "outcomesObjectives" : "Achieve sustainable development; Accelerate electrified transportation", "qualificationsBasic" : "Master’s Degree or higher, 5 years in product development, Demonstrated ability to manage engineering projects, Ability to work effectively across functions, Manage large teams, Willingness to travel", "qualificationsPreferred" : "Materials Science, Chemical Engineering, Lithium-ion battery cell technology, Engineering and project management roles", "workSiteFlexibility" : "Onsite", "rawDescription" : "Gotion Inc. is based in Silicon Valley, CA, currently building a Manufacturing facility in Manteno, IL and has R&D centers in Ohio, China, Japan and Europe. We innovate in the next generation electric vehicle and energy storage technologies (lithium batteries and related systems) with the aim to accelerate electrified transportation and achieve sustainable development. Gotion is powered by a leading power battery technology company that provides solutions for vehicles including the world's first mass commercial e-bus route. Gotion is a career destination - we are not simply attempting to just fill another job, but to pursue a dream of global green energy together! We offer outstanding opportunities to individuals seeking an exciting and challenging working environment. Everyone is highly valued and plays a vital role in the growth of our organization. Gotion is seeking a Technical Program Manager to spearhead US OEM customer projects in cell product development. In this role, you will lead the initiatives from concept through to production, coordinating closely with both our customers and our headquarter cell team. This position is ideal for someone with a robust engineering background and a masterful grasp of project management in the battery cell technology sector. Essential Duties and Responsibilities: Directly engage with US OEM customers, driving and coordinating cell development and manufacturing in tandem with the headquarter cell team. Manage projects from conception to production handover, acting as the main point of contact throughout the process. Develop detailed manufacturing program plans, defining strategy, scope, schedule, resources, and cost targets. Collaborate with cross-functional teams to align the manufacturing program with the planned objectives. Create, maintain, and effectively communicate project schedules to engineering leadership. Identify innovative solutions to overcome project obstacles and maintain schedule adherence. Prioritize and track the progress of cross-functional team tasks, balancing schedule, risk, resources, and outcomes. Qualifications: Required Qualifications: Master’s Degree or higher in Materials Science, Chemical Engineering, or a related field. Extensive knowledge and strong industry experience in lithium-ion battery cell technology. Minimum of 5 years in product development or manufacturing, with a mix of engineering and project management roles. Demonstrated ability to manage engineering projects for mass-produced products. Proficiency in project management tools like JIRA, Microsoft Project, and Confluence. Ability to work effectively across functions and manage large teams. Willingness to travel as required for project needs. Base pay is one part of our total compensation package at Gotion, and is determined within a range. This provides you with the opportunity to progress as you grow and advance your career at Gotion. The base pay range for this role is shown below, and will depend on your skills, qualifications, experiences, and location. Expected Pay Range $100,000—$200,000 USD Gotion Inc. is proud to be an equal opportunity employer. We are dedicated to fostering a diverse workforce that reflects the communities we serve, cultivating a culture of inclusion and belonging, and ensuring equal employment opportunities for all. We provide equal opportunity to all individuals regardless of race, creed, color, religion, gender, sexual orientation, gender identity or expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related conditions (including breastfeeding), parental status, criminal histories consistent with legal requirements, or any other characteristic protected by law. At Gotion Inc., we strive to create an environment where everyone feels valued, respected, and empowered to thrive.", "summaryDescription" : "Technical Program Manager, Cell Product at Gotion, Inc.. Skills: Cell product development, Project management. Engage with US OEM customers. Drive cell development", "postedDate" : "2026-06-13T21:09:57.546", "createdAt" : "2026-06-13T21:09:57.546", "lastUpdated" : "2026-06-15T07:22:56.222", "ingestTimestamp" : "2026-06-13T21:09:57.546", "mongoId" : "6a2c7ae874d8ee00a09475f2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 100000, "salaryAnnualMax" : 200000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Battery cell technology", "Cell product development", "Project management", "Cross-functional team management", "Program planning", "Schedule adherence", "Resource balancing", "Lithium-ion battery cell technology", "Electric vehicle technology", "Energy storage technologies", "JIRA", "Microsoft Project", "Confluence" ], "skillCount" : 13, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "_score" : 759.5895, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ca53d74d8ee00a09b559d", "title" : "Trial Attorney", "company" : "Carr Allison", "industry" : "Legal", "salary" : { "min" : 155000.0, "max" : 230000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimation is based on the 2024-2025 market baseline for a Lead Trial Attorney in Orlando, Florida, with adjustments for the legal industry and mid-level experience." }, "location" : "Orlando", "locations" : [ "Orlando" ], "timestamp" : "2026-06-16T04:41:54.269", "fingerprint" : "c26bd7ff23ac097de1be068ddfab53accd5374304a2683938bacacd64c75b37c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/carrallison/jobs/4092585009", "externalId" : "4092585009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Orlando", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "28.5421218,-81.3790450" } ], "locationText" : "Orlando, Florida, United States", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "professionalSkills" : [ "Civil litigation", "Case management", "Legal analysis", "Risk management", "Compliance oversight" ], "hardSkillsList" : [ "Pleadings drafting", "Motions drafting", "Discovery drafting", "Document review", "Case triage" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Pleadings drafting", "level" : "intermediate" }, { "name" : "Motions drafting", "level" : "intermediate" }, { "name" : "Discovery drafting", "level" : "intermediate" }, { "name" : "Document review", "level" : "intermediate" }, { "name" : "Case triage", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Trial preparation, Expert deposition, Caseload management", "majorSkillsList" : [ "Trial preparation", "Expert deposition", "Caseload management" ], "coreResponsibilities" : "Manage caseload, Draft pleadings, Draft motions, Draft discovery, Conduct document review, Perform case triage, Prepare for trial, Take active role in trials, Depose medical experts, Depose biomechanical experts, Serve as resource for associates, Mentor associates", "teamCollaboration" : "Collaborative culture; Team-oriented culture; Connected team", "domainKnowledge" : "Premises liability; Motor vehicle accidents", "domainList" : [ "premises-liability", "motor-vehicle-accidents" ], "domainSpecificKnowledge" : [ "Premises liability", "Motor vehicle accidents" ], "continuousLearning" : "Professional growth; Leadership development", "qualificationsBasic" : "Trial experience required, Manage caseload independently, Meet deadlines, Leadership potential", "qualificationsPreferred" : "Bodily injury litigation experience, Auto liability experience preferred, Premises liability experience preferred, Deposing medical experts valued, Deposing biomechanical experts valued", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Carr Allison is a well-regarded civil litigation firm, boasting a team of over 150 attorneys across the Southeast. Our unique philosophy of “early identification – early resolution” has earned us decades of trust and respect from our clients. At Carr Allison, our success is fueled by the collective efforts of our team and we believe that an open-door policy is essential to our continued growth. We proudly champion teamwork, collaboration, and the pursuit of excellence as cornerstones of our firm's culture. Join a team where your growth is our priority and your work truly matters. We are seeking a Trial Attorney to join our Orlando team. This attorney will manage a caseload of premises liability and motor vehicle accident cases for corporate clients. The ideal candidate has significant civil litigation experience and has taken an active role in at least two trials. Experience deposing medical or biomechanical experts is highly valued. Responsibilities: Handle a manageable caseload with full autonomy. Draft pleadings, motions, and discovery. Conduct document review and case triage. Engage in trial preparation and take an active role in trials. Depose medical and biomechanical experts as needed. Serve as a key resource and mentor for associates in the Orlando office. Qualifications: Trial experience is required. Bodily injury litigation experience, with auto or premises liability experience preferred. Ability to manage a caseload independently and meet deadlines. Leadership potential and willingness to be a go-to resource for the team. Office Culture: We are a growing office focused on building a collaborative, team-oriented culture. This role offers the opportunity to be a leader within the office and support our efforts to create a strong, connected team. Professional growth and leadership development are core priorities. For more information, please reach out to Smith Busby at sbusby@carrallison.com. Be part of a firm that values your potential and empowers your success.", "summaryDescription" : "Trial Attorney at Carr Allison. Skills: Trial preparation, Expert deposition, Caseload management. Manage caseload. Draft pleadings", "postedDate" : "2026-06-14T18:04:09.896", "createdAt" : "2026-06-14T18:04:09.896", "lastUpdated" : "2026-06-16T04:41:54.269", "ingestTimestamp" : "2026-06-14T18:04:09.896", "mongoId" : "6a2ca53d74d8ee00a09b559d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 155000, "salaryAnnualMax" : 230000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Pleadings drafting", "Motions drafting", "Discovery drafting", "Document review", "Case triage", "Leadership", "Mentoring", "Trial preparation", "Expert deposition", "Caseload management", "Civil litigation", "Case management", "Legal analysis", "Risk management", "Compliance oversight", "Premises liability", "Motor vehicle accidents" ], "skillCount" : 17, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "_score" : 753.60095, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Legal", "llmIndustryConfidence" : 0.98 }, { "id" : "69dde45b2beec4dd3d9a3f3e", "title" : "VP, Clinical Trials Operations", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 350000.0, "max" : 550000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a VP of Clinical Trials Operations in Duarte, California, adjusted for executive seniority and the healthcare industry." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Clinical Trials Operations", "Onsite, Days, Days" ], "timestamp" : "2026-06-15T09:04:30.110", "fingerprint" : "0917e0b94e44110bcc52509dde6ee546bd687ab43edcb6dcf474046f9f4b4425", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=231584", "externalId" : "231584", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1394513,-117.9772873" } ], "locationText" : "Duarte, California, United States", "minimumEducation" : "Master's", "experienceMinYears" : 15, "experienceMaxYears" : 99, "experienceLevel" : "Executive", "domainKnowledge" : "Oncology clinical research; Clinical trials operations; FDA regulations; GCP; HIPAA; NCI CCSG guidelines; Clinical research operations", "domainList" : [ "oncology-clinical-research", "clinical-trials-operations", "fda-regulations", "gcp", "hipaa", "nci-ccsg-guidelines", "clinical-research-operations" ], "domainSpecificKnowledge" : [ "Oncology clinical research", "Clinical trials operations", "FDA regulations", "GCP", "HIPAA", "NCI CCSG guidelines", "Clinical research operations" ], "remoteFriendly" : false, "rawDescription" : "Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. About the Role The Vice President, Clinical Trial Operations (VP CTO) provides strategic, operational, and executive leadership for all clinical research conducted across City of Hope’s national system. This leader oversees systemwide clinical research implementation, standardization, care delivery, workflow optimization, and performance improvement to ensure every patient—regardless of location—has access to high-quality clinical trials. As a successful candidate, you will: Operational Strategy & Leadership Oversee systemwide implementation of standardized workflows, technology integration, and operational processes that support clinical trial growth and excellence. Build strong relationships with internal and external stakeholders, including disease program leaders, PIs, foundation leadership, and sponsors. Guide systemwide strategic planning, goal setting, reporting, and process alignment to support clinical research expansion. Increase clinical research accrual through aligned processes, high-quality operations, and effective communication across the enterprise. Personnel Leadership Recruit, develop, and oversee clinical research personnel systemwide, ensuring adequate staffing, training, licensure, and performance standards. Develop staffing plans and manage performance improvement initiatives for all direct and indirect reports Provide coaching, development, and advancement opportunities for high-performing team members. Clinical Research Execution Establish and maintain systemwide standards for trial execution, patient safety, protocol compliance, and accurate data collection. Ensure strong relationships across clinical research teams and support high-quality patient care. Identify and implement SOPs and quality standards across research operations. Fiscal & Budget Oversight Develop and manage budgets, monitor financial performance, and identify opportunities for improved efficiency and cost savings. Collaborate on new programs and services that support the growth of clinical research across the system. Training, Quality & Performance Improvement Lead the development of systemwide onboarding, training, and continuous education programs for clinical research staff. Develop performance metrics and drive quality improvement initiatives. Ensure adherence to regulatory standards and lead systemwide performance improvement activities. Analyze data, define outcomes, and recommend strategies that improve patient experience and operational efficiency. Clinical Research Care Coordination Oversight Advance a culture of excellence in research practice and ensure seamless coordination of clinical research activity across all COH sites. Align trial openings with population needs and site resources. Build strategic partnerships with investigators, physicians, sponsors, cancer center leadership, and cross-functional departments. Your qualifications should include: Minimum Education Master’s degree in Nursing, Business Management, or related field Minimum Experience 15+ years of oncology clinical research experience , focused on clinical trials operations and patient-centered excellence. 15+ years of clinical trials management experience in an academic setting. Experience leading multidisciplinary clinical research teams. Deep knowledge of FDA regulations, GCP, HIPAA, NCI CCSG guidelines, and clinical research operations.. Preferred Experience Experience with Lean, Six Sigma, PDCA, and performance improvement methodologies. Proven leadership, project management, analytic, and communication skills. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "VP, Clinical Trials Operations at City of Hope", "createdAt" : "2026-06-14T04:50:35.613", "lastUpdated" : "2026-06-15T09:04:30.110", "ingestTimestamp" : "2026-06-14T04:50:35.613", "mongoId" : "69dde45b2beec4dd3d9a3f3e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 350000, "salaryAnnualMax" : 550000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Oncology clinical research", "Clinical trials operations", "FDA regulations", "GCP", "HIPAA", "NCI CCSG guidelines", "Clinical research operations" ], "skillCount" : 7, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "VP", "dataQualityScore" : 0.7777778, "_score" : 751.3353, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c6a8f74d8ee00a090c9c7", "title" : "Manager/Sr. Manager, Clinical Operations", "company" : "LifeMine Therapeutics", "industry" : "Biotech", "salary" : { "min" : 155000.0, "max" : 215000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Biotech industry in the United States, adjusted for Manager seniority in the Boston-Cambridge metro area." }, "location" : "Watertown, Massachusetts, United States", "locations" : [ "Watertown", "Massachusetts", "United States" ], "timestamp" : "2026-06-16T01:29:08.969", "fingerprint" : "097231c3c7e25bdd268e5eaee66838b2aac553ce796366030c3cda82d76ccb55", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/lifeminetx/jobs/8587930002", "externalId" : "8587930002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Watertown", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3652576,-71.1843234" } ], "locationText" : "Watertown, Massachusetts, United States", "minimumEducation" : "Bachelor's", "experienceMinYears" : 3, "experienceLevel" : "Manager", "professionalSkills" : [ "Contract negotiation", "Performance oversight" ], "hardSkillsList" : [ "Clinical trial design", "Clinical trial execution", "Regulatory requirements" ], "softSkillsList" : [ "Leadership", "Problem-solving" ], "hardSkills" : [ { "name" : "Clinical trial design", "level" : "intermediate" }, { "name" : "Clinical trial execution", "level" : "intermediate" }, { "name" : "Regulatory requirements", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Problem-solving" } ], "majorSkills" : "Clinical operations management, Clinical trial execution, Vendor management", "majorSkillsList" : [ "Clinical operations management", "Clinical trial execution", "Vendor management" ], "coreResponsibilities" : "Manage clinical trials execution, Provide strategic oversight, Oversee operational aspects, Develop protocols, Select sites, Negotiate contracts, Manage vendors, Manage monitoring activities, Manage data collection, Set-up clinical trial trackers, Update clinical trial trackers, Work with cross-functional teams, Ensure documentation submission, Develop clinical trial processes, Implement risk management strategies, Implement monitoring plans, Implement quality assurance initiatives, Track clinical trial progress, Report on clinical trial progress, Address trial issues, Address trial risks, Act as liaison, Ensure effective communication, Ensure timely decision-making, Stay up-to-date with industry trends, Stay up-to-date with regulatory changes, Stay up-to-date with best practices, Drive continuous improvement", "teamCollaboration" : "Cross-functional teams; External vendors; Clinical trial sites", "projectManagementSkills" : [ "Clinical trial management" ], "domainKnowledge" : "Good Clinical Practices; GCP; FDA; EMA; ICH-GCP; Clinical development lifecycle", "domainList" : [ "good-clinical-practices", "gcp", "fda", "ema", "ich-gcp", "clinical-development-lifecycle" ], "domainSpecificKnowledge" : [ "Good Clinical Practices", "GCP", "FDA", "EMA", "ICH-GCP", "Clinical development lifecycle" ], "documentationSkills" : "Clinical trial documentation", "continuousLearning" : "Stay up-to-date with industry trends; Stay up-to-date with regulatory changes; Stay up-to-date with clinical trial best practices", "problemSolvingSkills" : "Problem-solving skills", "specialRequirements" : "Ability to travel as needed", "outcomesObjectives" : "Ensuring successful delivery on time; Ensuring successful delivery within budget", "qualificationsBasic" : "Bachelor's or Master's degree, 3 years of experience in clinical operations, 5 years of experience in clinical operations, Knowledge of clinical trial design, Knowledge of clinical trial execution, Knowledge of regulatory requirements, Managing multi-site clinical trials, Experience working with CROs, Experience working with vendors, Experience working with clinical trial sites, Contract negotiation, Performance oversight, Proficiency in clinical trial management systems", "qualificationsPreferred" : "Master's degree in Life Sciences", "rawDescription" : "What’s the opportunity? LifeMine Therapeutics is seeking an experienced and results-driven Manager/Sr Manager, Clinical Operations to join our growing Clinical Development team. Reporting to the Director of Clinical Operations, this individual will play a key role in the planning, execution, and management of clinical trials, ensuring successful delivery on time and within budget, while adhering to regulatory requirements and company objectives. The Manager/Sr Manager will work cross-functionally with R&D and external vendors, providing leadership and oversight throughout the clinical development lifecycle. Key Responsibilities: Manage the execution of clinical trials, ensuring that trials are conducted according to the highest standards, in compliance with Good Clinical Practices (GCP), and within timelines and budget. Provide strategic oversight and direction for clinical operations, ensuring alignment with corporate objectives and regulatory requirements. Oversee the operational aspects of clinical studies, including protocol development, site selection, contract negotiations, vendor management, monitoring activities, and data collection. Set-up and update clinical trial-related trackers such as startup progress, screening/enrollment, study invoices/payments, etc. Work closely with cross-functional teams to ensure smooth integration of all clinical operations activities. Ensure timely preparation and submission of clinical trial-related documentation to regulatory agencies and ethics committees. Develop and implement clinical trial processes, including risk management strategies, monitoring plans, and quality assurance initiatives. Track and report on clinical trial progress, identifying and addressing any issues or risks that could impact trial milestones. Act as a liaison between external vendors, sites, and LifeMine leadership to ensure effective communication and timely decision-making. Stay up-to-date with industry trends, regulatory changes, and clinical trial best practices to drive continuous improvement within the organization. What you will need to be successful: Bachelor’s or Master’s degree in Life Sciences or a related field Minimum of 3 (Manager)/ 5 (Sr. Manager) years of experience in clinical operations within the pharmaceutical or biotechnology industry. Strong knowledge of clinical trial design, execution, and regulatory requirements (FDA, EMA, ICH-GCP). Proven track record of managing multi-site, complex clinical trials from start-up to completion. Experience working with CROs, vendors, and clinical trial sites, including contract negotiation and performance oversight. Excellent organizational, leadership, and communication skills with the ability to manage cross-functional teams effectively. Strong problem-solving skills, with the ability to identify and address challenges in a fast-paced, dynamic environment. Ability to manage multiple priorities and deadlines, while maintaining a high level of attention to detail. Proficiency in clinical trial management systems (CTMS) and other relevant software tools. Ability to travel as needed for site visits, meetings, and other clinical operations activities.", "summaryDescription" : "Manager/Sr. Manager, Clinical Operations at LifeMine Therapeutics. Skills: Clinical operations management, Clinical trial execution, Vendor management. Manage clinical trials execution. Provide strategic oversight", "postedDate" : "2026-06-14T21:46:00.628", "createdAt" : "2026-06-14T21:46:00.628", "lastUpdated" : "2026-06-16T01:29:08.969", "ingestTimestamp" : "2026-06-14T21:46:00.628", "mongoId" : "6a2c6a8f74d8ee00a090c9c7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 155000, "salaryAnnualMax" : 215000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Clinical trial design", "Clinical trial execution", "Regulatory requirements", "Leadership", "Problem-solving", "Clinical operations management", "Vendor management", "Contract negotiation", "Performance oversight", "Clinical trial management", "Good Clinical Practices", "GCP", "FDA", "EMA", "ICH-GCP", "Clinical development lifecycle" ], "skillCount" : 16, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 0.8888889, "_score" : 749.6591, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.97 }, { "id" : "6a3091ccf292fd229c0bffdc", "title" : "Clinical Study Coordinator", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 65000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Clinical Study Coordinator in Cleveland, OH, adjusted for mid-seniority and full-time employment in the healthcare industry." }, "location" : "Cleveland, Tennessee, United States", "locations" : [ "Cleveland", "Tennessee", "United States" ], "certifications" : [ "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA" ], "timestamp" : "2026-06-16T12:06:19.361", "fingerprint" : "b3432dca3c44d9d9df1da4145df70df9f4cf3adcde1c8594ac6fc88093036adf", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000132293869-clinical-study-coordinator-", "externalId" : "744000132293869", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Cleveland", "state" : "Tennessee", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.1595182,-84.8766115" }, { "city" : "Athens", "state" : "Tennessee", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.4428864,-84.5930113" }, { "city" : "Chattanooga", "state" : "Tennessee", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.0457219,-85.3094883" } ], "locationText" : "Cleveland, Tennessee, United States; Athens, Tennessee, United States; Chattanooga, Tennessee, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Study coordination", "Data entry", "Protocol management", "Regulatory document submission", "Site management" ], "hardSkillsList" : [ "Clinical trial coordination", "Patient recruitment", "Informed consent process", "Laboratory processing", "Investigational product handling", "Budget negotiation", "Regulatory compliance", "IRB submission" ], "softSkillsList" : [ "Mentoring" ], "hardSkills" : [ { "name" : "Clinical trial coordination", "level" : "intermediate" }, { "name" : "Patient recruitment", "level" : "intermediate" }, { "name" : "Informed consent process", "level" : "intermediate" }, { "name" : "Laboratory processing", "level" : "intermediate" }, { "name" : "Investigational product handling", "level" : "intermediate" }, { "name" : "Budget negotiation", "level" : "intermediate" }, { "name" : "Regulatory compliance", "level" : "intermediate" }, { "name" : "IRB submission", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Mentoring" } ], "majorSkills" : "Clinical study coordination, Site support, Regulatory compliance", "majorSkillsList" : [ "Clinical study coordination", "Site support", "Regulatory compliance" ], "coreResponsibilities" : "Support medical institution in clinical trial-related activities, Assess feasibility of new/potential clinical studies, Conduct research-related visits, Assist with logistics of scheduling research visits, Collaborate with ancillary departments for patient flow, Perform general study conduct tasks, Enter data into study related EDC systems, Resolve study specific issues, Mentor staff, Perform administrative tasks, Act as line of communication between Milestone One,, Facilitate evaluation of proposed studies, Provide responses to feasibility questions, Participate in patient recruitment/identification, Confirm eligibility for study inclusion, Assist with plan development for recruitment/retention tools, Assist with obtaining informed consent, Obtain required assessments at each visit, Notify investigator of critical values, Obtain laboratory testing, processing, and shipping, Assist in scheduling and preparation for sponsor/CRO representative, Track patient recruitment and enrollment, Support site team to ensure enrollment targets are, Provide regular updates on study amendments, Ensure accurate and timely data entry into EDC, Resolve data queries, Assist in reporting and following up on adverse, Assist in reporting and following up on protocol, Support handling, accountability, and reconciliation of investigational products, Maintain study blinding, Follow protocol/sponsor/CRO guidance for unblinding, Assist site staff with temperature monitoring for study, Support contract and budget negotiations, Oversee Investigator/Site Payments, Ensure staff complete necessary training, Complete retraining for protocol changes, Ensure investigator reviews and signs study documents, Educate site research team on clinical trial requirements, Maintain study documents for visits/audits/inspections, Prepare and submit regulatory documents to regulatory authorities, Prepare and submit correspondence to institutional review boards, Participate in on-site training of additional staff, Identify areas for site improvement, Develop tools to assist with improvements, Maintain licensure and certifications", "teamCollaboration" : "Cross-functional teams; Ancillary departments; Sponsor representatives; CRO representatives; Medical institution staff; Investigators", "domainKnowledge" : "Clinical trial conduct; Human subjects research; Good Clinical Practice (GCP); Study protocols; Inclusion/exclusion criteria; Adverse events; Protocol deviations; Investigational products; Site SOPs; Lab manuals; Regulatory authorities; Institutional Review Boards (IRBs)", "domainList" : [ "clinical-trial-conduct", "human-subjects-research", "good-clinical-practice-gcp", "study-protocols", "inclusion-exclusion-criteria", "adverse-events", "protocol-deviations", "investigational-products", "site-sops", "lab-manuals", "regulatory-authorities", "institutional-review-boards-irbs" ], "domainSpecificKnowledge" : [ "Clinical trial conduct", "Human subjects research", "Good Clinical Practice (GCP)", "Study protocols", "Inclusion/exclusion criteria", "Adverse events", "Protocol deviations", "Investigational products", "Site SOPs", "Lab manuals", "Regulatory authorities", "Institutional Review Boards (IRBs)" ], "toolProficiency" : [ "EDC systems" ], "documentationSkills" : "Source documentation; Study documents; Regulatory documents", "innovationCreativity" : "Develop tools to assist with improvements", "problemSolvingSkills" : "Resolve study specific issues; Resolve data queries", "specialRequirements" : "On-site daily at Cleveland site, Occasional travel to Athens and Chattanooga sites", "outcomesObjectives" : "Ensure enrollment targets are met; Ensure accurate and timely data entry; Ensure staff complete necessary training", "qualificationsBasic" : "Two years of experience coordinating clinical research studies involving human subjects, On-the-job training with at least two years of experience coordinating clinical research studies involving human subjects", "qualificationsPreferred" : "Nephrology experience preferred, Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. Tasks may include activities associated with the assessment of the feasibility of new/potential clinical studies, conducting research-related visits as outlined in the respective protocol, assisting the site with logistics of scheduling research visits and testing per the schedule of events in the protocol, collaboration with ancillary departments involved in the research visit to assist in a smooth patient flow at research visits., general study conduct tasks, assistance with data entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In addition, mentoring staff and administrative tasks as assigned by the Milestone One Manager. In this job you will: * Acts as a constant line of communication between Milestone One, the Sponsor or CRO, and the medical institution. * Facilitates the evaluation of proposed studies and ensures responses to feasibility questions are provided in due time. * Actively participates in patient recruitment/identification and evaluation for study inclusion by confirming eligibility according to the Inclusion and exclusion criteria. * Assists with plan development for new recruitment / retention tools, source documentation and other site tools to enhance quality and time management of research staff. * Assists the local research team in obtaining informed consent before study entry or any study-related procedures or tests being performed. * Assist with obtaining the required assessments at each visit per the protocol and notify the investigator of any critical values that need immediate attention or would prohibit or delay study treatment. * Assist with obtaining local and central laboratory testing, processing, and shipping per site SOP and study-specific lab manual. * Assist in scheduling and preparation for all types of sponsors or CRO representative visits at the medical institution. * Track patient recruitment and enrollment and actively supports the medical site team to ensure enrollment targets are met at the site level. Provides regular updates to the staff and investigators regarding study amendments. * Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to guidelines and investigator instructions. * Support proper handling, accountability, and reconciliation of all investigational products and clinical supplies. If applicable, always maintain the study blinding. Protocol and sponsor/CRO guidance will be followed if a study participant requires unblinding. * Assist site staff with maintaining appropriate temperature monitoring for study products and supplies. * Support the contract and budget negotiations and oversees Investigator/Site Payments. * Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial. Retraining will be completed for changes to the protocol before site implementation. * Be responsible for ensuring the investigator reviews and signs study documents appropriately and within a reasonable period. Guidance should be provided to educate the site research team on requirements for conducting clinical trials, date format, etc. * Actively participate in maintaining study documents at the medical institution in preparation for on-site study visits/audits or regulatory agency inspections. * Assist with preparing and submitting regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs). * May be involved in the on-site training of additional staff as part of the SEO or other education programs. * Assist with identifying areas that need improvement for specific sites and assists with developing tools to assist with improvements. * Maintain all licensure and certifications applicable to the role of SEO site/Study coordinator II. * SEO SC is responsible for only performing assigned tasks within their training and licensure if applicable. SEO SC should immediately consult the assigned Milestone One manager for tasks that do not fall within their scope. ## Qualifications Education Relevant education and at least two years of experience coordinating clinical research studies involving human subjects OR, if allowed by local regulations, on-the-job training with at least two years of experience coordinating clinical research studies involving human subjects. Nephrology experience preferred. Certifications * Current Good Clinical Practice (GCP) * International Air Transport Association (IATA) * Current Basic Cardiopulmonary Resuscitation (CPR) * Phlebotomy certification unless part of active professional licensure (RN or LPN) * Preferred Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization. May be obtained within (1) year of employment or status change if not currently certified. ## Additional Information Location: Tennessee region. This role requires being on-site daily at the Cleveland site, with occasional travel to the Athens and Chattanooga sites. If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you!", "summaryDescription" : "Clinical Study Coordinator at PSI CRO. Skills: Clinical study coordination, Site support, Regulatory compliance. Support medical institution in clinical trial-related activities. 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Athens, Tennessee, United States; Chattanooga, Tennessee, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Study coordination", "Data entry", "Protocol execution", "Regulatory document preparation", "Site management" ], "hardSkillsList" : [ "Clinical trial coordination", "Patient recruitment", "Informed consent process", "Laboratory processing", "Investigational product handling", "Study blinding", "Regulatory submissions", "IRB submissions" ], "softSkillsList" : [ "Mentoring" ], "hardSkills" : [ { "name" : "Clinical trial coordination", "level" : "intermediate" }, { "name" : "Patient recruitment", "level" : "intermediate" }, { "name" : "Informed consent process", "level" : "intermediate" }, { "name" : "Laboratory processing", "level" : "intermediate" }, { "name" : "Investigational product handling", "level" : "intermediate" }, { "name" : "Study blinding", "level" : "intermediate" }, { "name" : "Regulatory submissions", "level" : "intermediate" }, { "name" : "IRB submissions", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Mentoring" } ], "majorSkills" : "Clinical study coordination, Site support, Regulatory compliance", "majorSkillsList" : [ "Clinical study coordination", "Site support", "Regulatory compliance" ], "coreResponsibilities" : "Support medical institution in clinical trial-related activities, Assess feasibility of new/potential clinical studies, Conduct research-related visits, Assist with logistics of scheduling research visits, Assist with testing per schedule of events, Collaborate with ancillary departments for patient flow, Perform general study conduct tasks, Assist with data entry into EDC systems, Contact CRO or sponsor representatives to schedule monitoring, Resolve study specific issues, Mentor staff, Perform administrative tasks, Act as communication line between Milestone One, Sponsor/CRO,, Facilitate evaluation of proposed studies, Ensure responses to feasibility questions are provided, Participate in patient recruitment/identification, Confirm eligibility for study inclusion, Assist with plan development for recruitment/retention tools, Assist with plan development for source documentation, Assist with plan development for site tools, Assist research team in obtaining informed consent, Assist with obtaining required assessments at each visit, Notify investigator of critical values, Assist with obtaining laboratory testing, Assist with processing laboratory samples, Assist with shipping laboratory samples, Assist in scheduling sponsor or CRO representative visits, Assist in preparation for sponsor or CRO representative, Track patient recruitment and enrollment, Support site team to ensure enrollment targets are, Provide regular updates on study amendments, Ensure accurate data entry into EDC systems, Resolve data queries, Assist in reporting adverse events, Assist in reporting protocol deviations, Follow up on adverse events, Follow up on protocol deviations, Support handling of investigational products, Support accountability of investigational products, Support reconciliation of investigational products, Maintain study blinding, Follow protocol/sponsor/CRO guidance for unblinding, Assist site staff with temperature monitoring for study, Assist site staff with temperature monitoring for study, Support contract negotiations, Support budget negotiations, Oversee Investigator/Site Payments, Ensure staff complete necessary study-specific training, Ensure staff complete general training, Complete retraining for protocol changes, Ensure investigator reviews and signs study documents, Provide guidance on conducting clinical trials, Educate site research team on requirements, Participate in maintaining study documents, Prepare for on-site study visits/audits, Prepare for regulatory agency inspections, Prepare and submit regulatory documents, Prepare and submit correspondence to regulatory authorities, Prepare and submit correspondence to institutional review boards, Involved in on-site training of additional staff, Identify areas needing improvement for specific sites, Develop tools to assist with improvements, Maintain all licensure and certifications applicable to the, Perform assigned tasks within training and licensure", "teamCollaboration" : "Communication with Sponsor or CRO; Collaboration with ancillary departments; Coordination with site staff; Liaison with regulatory authorities; Liaison with IRBs", "projectManagementSkills" : [ "Study conduct management", "Enrollment target management", "Training management" ], "domainKnowledge" : "Clinical trial protocols; Study-specific lab manuals; Good Clinical Practice (GCP)", "domainList" : [ "clinical-trial-protocols", "study-specific-lab-manuals", "good-clinical-practice-gcp" ], "domainSpecificKnowledge" : [ "Clinical trial protocols", "Study-specific lab manuals", "Good Clinical Practice (GCP)" ], "toolProficiency" : [ "EDC systems" ], "communicationSkills" : "Line of communication; Provide updates", "documentationSkills" : "Source documentation; Study documents; Regulatory documents", "innovationCreativity" : "Develop tools to assist with improvements", "problemSolvingSkills" : "Resolve study specific issues; Resolve data queries", "specialRequirements" : "On-site daily at Cleveland site, Occasional travel to Athens and Chattanooga sites", "outcomesObjectives" : "Ensure enrollment targets are met; Ensure accurate and timely data entry; Ensure staff complete necessary training", "qualificationsBasic" : "Two years of experience coordinating clinical research studies involving human subjects, On-the-job training with at least two years of experience coordinating clinical research studies involving human subjects", "qualificationsPreferred" : "Nephrology experience, Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. Tasks may include activities associated with the assessment of the feasibility of new/potential clinical studies, conducting research-related visits as outlined in the respective protocol, assisting the site with logistics of scheduling research visits and testing per the schedule of events in the protocol, collaboration with ancillary departments involved in the research visit to assist in a smooth patient flow at research visits., general study conduct tasks, assistance with data entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In addition, mentoring staff and administrative tasks as assigned by the Milestone One Manager. In this job you will: * Acts as a constant line of communication between Milestone One, the Sponsor or CRO, and the medical institution. * Facilitates the evaluation of proposed studies and ensures responses to feasibility questions are provided in due time. * Actively participates in patient recruitment/identification and evaluation for study inclusion by confirming eligibility according to the Inclusion and exclusion criteria. * Assists with plan development for new recruitment / retention tools, source documentation and other site tools to enhance quality and time management of research staff. * Assists the local research team in obtaining informed consent before study entry or any study-related procedures or tests being performed. * Assist with obtaining the required assessments at each visit per the protocol and notify the investigator of any critical values that need immediate attention or would prohibit or delay study treatment. * Assist with obtaining local and central laboratory testing, processing, and shipping per site SOP and study-specific lab manual. * Assist in scheduling and preparation for all types of sponsors or CRO representative visits at the medical institution. * Track patient recruitment and enrollment and actively supports the medical site team to ensure enrollment targets are met at the site level. Provides regular updates to the staff and investigators regarding study amendments. * Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to guidelines and investigator instructions. * Support proper handling, accountability, and reconciliation of all investigational products and clinical supplies. If applicable, always maintain the study blinding. Protocol and sponsor/CRO guidance will be followed if a study participant requires unblinding. * Assist site staff with maintaining appropriate temperature monitoring for study products and supplies. * Support the contract and budget negotiations and oversees Investigator/Site Payments. * Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial. Retraining will be completed for changes to the protocol before site implementation. * Be responsible for ensuring the investigator reviews and signs study documents appropriately and within a reasonable period. Guidance should be provided to educate the site research team on requirements for conducting clinical trials, date format, etc. * Actively participate in maintaining study documents at the medical institution in preparation for on-site study visits/audits or regulatory agency inspections. * Assist with preparing and submitting regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs). * May be involved in the on-site training of additional staff as part of the SEO or other education programs. * Assist with identifying areas that need improvement for specific sites and assists with developing tools to assist with improvements. * Maintain all licensure and certifications applicable to the role of SEO site/Study coordinator II. * SEO SC is responsible for only performing assigned tasks within their training and licensure if applicable. SEO SC should immediately consult the assigned Milestone One manager for tasks that do not fall within their scope. ## Qualifications Education Relevant education and at least two years of experience coordinating clinical research studies involving human subjects OR, if allowed by local regulations, on-the-job training with at least two years of experience coordinating clinical research studies involving human subjects. Nephrology experience preferred. Certifications * Current Good Clinical Practice (GCP) * International Air Transport Association (IATA) * Current Basic Cardiopulmonary Resuscitation (CPR) * Phlebotomy certification unless part of active professional licensure (RN or LPN) * Preferred Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization. May be obtained within (1) year of employment or status change if not currently certified. ## Additional Information Location: Tennessee region. This role requires being on-site daily at the Cleveland site, with occasional travel to the Athens and Chattanooga sites. If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you!", "summaryDescription" : "Clinical Study Coordinator at PSI CRO. Skills: Clinical study coordination, Site support, Regulatory compliance. Support medical institution in clinical trial-related activities. Assess feasibility of new/potential clinical studies", "postedDate" : "2026-06-15T22:35:33.000", "createdAt" : "2026-06-16T01:44:49.930", "lastUpdated" : "2026-06-16T12:44:37.356", "ingestTimestamp" : "2026-06-16T01:44:49.930", "mongoId" : "6a3084c6f292fd229c075840", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 85000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Clinical trial coordination", "Patient recruitment", "Informed consent process", "Laboratory processing", "Investigational product handling", "Study blinding", "Regulatory submissions", "IRB submissions", "Mentoring", "Clinical study coordination", "Site support", "Regulatory compliance", "Study coordination", "Data entry", "Protocol execution", "Regulatory document preparation", "Site management", "Study conduct management", "Enrollment target management", "Training management", "Clinical trial protocols", "Study-specific lab manuals", "Good Clinical Practice (GCP)", "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "EDC systems" ], "skillCount" : 29, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "_score" : 748.61646, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69dde45b2beec4dd3d9a3efe", "title" : "Clinical Trials Data Coord", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 3500000.0, "max" : 5500000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Clinical Trials Data Coordinator in India, adjusted for the healthcare industry and remote work." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Clinical Research", "Remote, Days, Days" ], "certifications" : [ "GCP Professional Data Engineer", "AWS Data Analytics", "Databricks Certified", "Dbt Certified" ], "timestamp" : "2026-06-15T06:56:19.156", "fingerprint" : "4dbfb3c03e7dedbf592feae1ea9174ff2e33e59984b4087824c1b7465cbc9c01", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=232244", "externalId" : "232244", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 2, "technicalSkills" : "SQL, Python, R, Scala, Spark, Dbt, Snowflake, BigQuery, Redshift, Databricks, Fivetran, Airflow, Dbt Cloud, Delta Lake, Scikit-learn, TensorFlow, PyTorch, XGBoost, LightGBM, Hugging Face, MLflow, AWS, S3, Glue, SageMaker, Athena, GCP, Vertex AI, Azure, Synapse, ML Studio", "professionalSkills" : [ "Data abstraction", "Query resolution", "Data integrity", "Electronic records", "Patient information" ], "hardSkillsList" : [ "Statistical methods", "ML frameworks", "BI platforms", "Cloud data stacks", "Modelling skills", "Quantitative analysis" ], "hardSkills" : [ { "name" : "Statistical methods", "level" : "intermediate" }, { "name" : "ML frameworks", "level" : "intermediate" }, { "name" : "BI platforms", "level" : "intermediate" }, { "name" : "Cloud data stacks", "level" : "intermediate" }, { "name" : "Modelling skills", "level" : "intermediate" }, { "name" : "Quantitative analysis", "level" : "intermediate" } ], "majorSkills" : "Data science, Data engineering, ML/AI, Business intelligence, Analytics engineering", "majorSkillsList" : [ "Data science", "Data engineering", "ML/AI", "Business intelligence", "Analytics engineering" ], "coreResponsibilities" : "Ensure data integrity, Complete CRFs, Resolve queries, Coordinate sponsor visits, Maintain audit-ready data, Oversee electronic research records, Manage patient information", "teamCollaboration" : "Clinical research team", "domainKnowledge" : "Good Clinical Practices; FDA regulations; NIH guidelines; HIPAA regulations; Clinical research; Study protocols", "domainList" : [ "good-clinical-practices", "fda-regulations", "nih-guidelines", "hipaa-regulations", "clinical-research", "study-protocols" ], "domainSpecificKnowledge" : [ "Good Clinical Practices", "FDA regulations", "NIH guidelines", "HIPAA regulations", "Clinical research", "Study protocols" ], "toolProficiency" : [ "CTMS" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "CRF completion", "qualificationsBasic" : "Bachelor's Degree, 2 years relevant experience", "qualificationsPreferred" : "PhD preferred, GCP Professional Data Engineer, AWS Data Analytics, Databricks Certified, Dbt Certified", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Clinical Trials Data Coordinator - Remote Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. This full-time remote position entails ensuring data integrity for various research studies. Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data. You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research. As a successful candidate, you will: Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations. Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information. Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution. Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements. Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work. Qualifications - External Qualifications - External Qualifications - External Your qualifications should include: Bachelor’s Degree, relevant experience may substitute for degree. At least two years of experience related to the conduct of oncology clinical trials. Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Clinical Trials Data Coord at City of Hope. Skills: Data science, Data engineering, ML/AI, Business intelligence, Analytics engineering. Ensure data integrity. Complete CRFs", "createdAt" : "2026-06-14T07:53:46.055", "lastUpdated" : "2026-06-15T06:56:19.156", "ingestTimestamp" : "2026-06-14T07:53:46.055", "mongoId" : "69dde45b2beec4dd3d9a3efe", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Statistical methods", "ML frameworks", "BI platforms", "Cloud data stacks", "Modelling skills", "Quantitative analysis", "Data science", "Data engineering", "ML/AI", "Business intelligence", "Analytics engineering", "Data abstraction", "Query resolution", "Data integrity", "Electronic records", "Patient information", "Good Clinical Practices", "FDA regulations", "NIH guidelines", "HIPAA regulations", "Clinical research", "Study protocols", "GCP Professional Data Engineer", "AWS Data Analytics", "Databricks Certified", "Dbt Certified", "CTMS" ], "skillCount" : 27, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Junior", "dataQualityScore" : 0.7777778, "_score" : 744.5613, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69dde45b2beec4dd3d9a3ec7", "title" : "Sr Clinical Trials Data Coord", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 85000.0, "max" : 125000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline data for a Senior Clinical Trials Data Coordinator in the United States, adjusted for seniority and remote work." }, "location" : "US-Nationwide-USA-Remote-US-Remote", "locations" : [ "US-Nationwide-USA-Remote-US-Remote", "Research Data Management & Analysis", "Remote, Days, Days" ], "certifications" : [ "GCP training", "Human Subjects Protection training", "SOCRA certification", "ACRP certification" ], "timestamp" : "2026-06-15T04:54:39.396", "fingerprint" : "6fc0f7ab0f6b57f0c51e97503e48e8ec9abdbd885e41d949c49315d627794fd9", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=233629", "externalId" : "233629", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 7, "experienceLevel" : "Senior", "technicalSkills" : "CTMS, EDC, EMR", "professionalSkills" : [ "Data collection coordination", "Data entry", "Quality assurance", "Query resolution", "Regulatory compliance", "Study monitoring", "Adverse event management", "Data management planning", "Workflow development", "Peer data review" ], "hardSkillsList" : [ "Data accuracy", "Data completeness", "Data cleaning", "SAE follow-up", "Study calendar maintenance", "Financial trigger management", "Billing support" ], "hardSkills" : [ { "name" : "Data accuracy", "level" : "intermediate" }, { "name" : "Data completeness", "level" : "intermediate" }, { "name" : "Data cleaning", "level" : "intermediate" }, { "name" : "SAE follow-up", "level" : "intermediate" }, { "name" : "Study calendar maintenance", "level" : "intermediate" }, { "name" : "Financial trigger management", "level" : "intermediate" }, { "name" : "Billing support", "level" : "intermediate" } ], "majorSkills" : "Clinical trial data, Data quality, Regulatory compliance", "majorSkillsList" : [ "Clinical trial data", "Data quality", "Regulatory compliance" ], "coreResponsibilities" : "Enter and manage clinical trial data, Ensure data accuracy, completeness, and compliance, Maintain regulatory compliance, Collaborate with sponsors, physicians, and clinical coordinators, Resolve protocol issues and data discrepancies, Manage adverse event documentation and classification, Maintain study calendars, financial triggers, and data completion, Support monitoring visits, study initiation visits, audits, and, Assist with EDC builds, Create data standards, Prepare reports, Participate in CAPA and process improvement initiatives, Mentor peers", "teamCollaboration" : "Collaborate with physicians; Collaborate with clinical coordinators; Collaborate with research teams; Collaborate with sponsors", "domainKnowledge" : "Oncology clinical trials; Clinical research data management; FDA guidelines; ICH-GCP guidelines; ALCOA+; HIPAA; MedDRA; CTCAE; WHO-DDE", "domainList" : [ "oncology-clinical-trials", "clinical-research-data-management", "fda-guidelines", "ich-gcp-guidelines", "alcoa", "hipaa", "meddra", "ctcae", "who-dde" ], "domainSpecificKnowledge" : [ "Oncology clinical trials", "Clinical research data management", "FDA guidelines", "ICH-GCP guidelines", "ALCOA+", "HIPAA", "MedDRA", "CTCAE", "WHO-DDE" ], "toolProficiency" : [ "OnCore" ], "documentationSkills" : "Data management plans; Study documentation", "problemSolvingSkills" : "Query resolution; Discrepancy resolution", "outcomesObjectives" : "Ensure accurate, reliable, and compliant research data; Maintain high-quality clinical trial data; Ensure efficient research operations", "qualificationsBasic" : "Bachelor's degree in Science, 5-7 years clinical research experience, GCP training completion, Human Subjects Protection training", "qualificationsPreferred" : "Ability to obtain SOCRA certification, Ability to obtain ACRP certification", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. The Senior Clinical Trials Data Coordinator supports complex oncology clinical trials from First-in-Human and Phase I through Phase IV by coordinating data collection, entry, quality assurance, and query resolution to ensure accurate, reliable, and compliant research data. The role involves interpreting research protocols, reviewing medical records, resolving discrepancies, and maintaining study visits and financial triggers within the Clinical Trial Management System (CTMS) aligned with Electronic Data Capture (EDC) systems. Working closely with physicians, clinical coordinators, and research teams, the coordinator ensures timely data reporting, supports adverse event data collection, and contributes to study monitoring and regulatory compliance. Additionally, the role includes performing peer data reviews, assisting in the development of data management plans and workflows, and providing training and guidance to research data staff to maintain high-quality clinical trial data and efficient research operations. As a successful candidate, you will: Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. Ensure data accuracy, completeness, and compliance through quality checks, data cleaning, and timely resolution of queries. Maintain regulatory compliance with FDA, ICH-GCP, ALCOA+, HIPAA, and other applicable guidelines for clinical research data management. Collaborate with sponsors, physicians, and clinical coordinators to resolve protocol issues, data discrepancies, and ensure proper documentation. Manage adverse event documentation and classification using standard dictionaries such as MedDRA, CTCAE, and WHO-DDE, including SAE follow-up and query resolution. Maintain study calendars, financial triggers, and data completion tracking in CTMS to support billing and study financial management. Support monitoring visits, study initiation visits, audits, and inspection readiness, ensuring data quality and completeness. Contribute to data management improvements by assisting with EDC builds, creating data standards, preparing reports, participating in CAPA and process improvement initiatives, and mentoring peers. Qualifications - External Your qualifications should include: Minimum Education Bachelor’s degree in Science, Health, or a related field from an accredited university, or equivalent relevant work experience. Minimum Experience : Minimum of 5–7 years of clinical research or related experience. Required Certifications: Completion of Good Clinical Practice (GCP) training within 1 month of employment. Completion of Human Subjects Protection (HSP) training within 1 month of employment. Ability to obtain SOCRA or ACRP certification within 2 years of employment. Systems Knowledge: Experience with Clinical Trial Management Systems (CTMS), Electronic Medical Records (EMR), and eRegulatory systems. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here . To learn more about our Comprehensive Benefits, please CLICK HERE . US-Nationwide-USA-Remote-US-Remote", "summaryDescription" : "Sr Clinical Trials Data Coord at City of Hope. Skills: Clinical trial data, Data quality, Regulatory compliance. Enter and manage clinical trial data. 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City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. The Senior Budget Administrator coordinates and oversees the development of coverage analyses and budgets for both industry sponsored and non-industry sponsored clinical trials. Works with third party vendors as necessary to supply clinical trial documentation, prioritize work queues, and assist with budget development. Negotiates budgets with clinical trial sponsors on behalf of the institution to ensure optimal cost efficiency. Tracks all relevant data and ensures both contracting and Revenue Integrity teams are supplied with finalized documentation. Enters, maintains and/or reviews financial data from finalized clinical trial agreements and budgets into the OnCore Clinical Trial Management System (CTMS). Provides day-to-day administrative support to Principal Investigators, clinical research nurses, research site managers, clinical research coordinators, departmental business directors and other stakeholders in resolving budget development issues, including but not limited to budget estimates and qualifying trial assessments. Charged with ensuring that incremental costs of clinical research are covered per institutional policies and guidelines while applying clinical research billing compliance expertise pertaining to all applicable payers. The position includes the general development and ongoing refinement of administrative infrastructure for the management of financial activity associated with for-profit corporate sponsorship as well as non-industry submissions pertaining to clinical trials. Provides guidance and serves as the point of contact for new and junior staff, specifically Budget Analysts and Coverage Analysts for financial related questions, engaging management as appropriate. Assist new/junior staff with prioritizing tasks. May provide training, onboarding and/or mentorship to new/junior staff; may have supervisory responsibilities. Ensures quality of the study start-up activities; as needed may conduct quality review and/or audits of clinical trial coverage analysis, budgets, clinical trial agreements and/or financial data entered in OnCore. As a successful candidate, you will: Coordinate with all relevant groups to draft, finalize, and gain approval of coverage analyses and budgets while tracking all appropriate data metrics. Review coding and charge determinations with PI and study team. Enter and/or review financial data in OnCore and initiate the sign-off process of the OnCore calendar/financial console. Perform critical assessment of each project to confirm funding source and negotiates consistently as per institutional guidelines. Perform detailed analyses of current budgets to establish precedent pricing and better budget development techniques. Assess comparable nature of projects by factors such as study phase or disease-type to ensure appropriate costing. Analyze new protocols, letters of intent, synopses, etc., received from sponsors, review committees or PI/study teams to determine coverage analysis/budget necessity and/or prioritization in coordination with department leadership. Interact with sponsor officials to solve budget issues such as budgetary changes, target patient accrual changes, requests for additional funds, or general cost disputes. Compile non-detailed budget estimates via internal estimation tools, as needed and when applicable to sponsor guidelines. Work with third-party vendors if detailed estimates are required Carry out periodic reviews of study files to ensure administrative quality, compliance, and consistency across clinical trials Review protocol amendments for any revisions affecting the budget; updates budget as necessary or re-prioritizes for additional development by a third-party vendor. Your qualifications should include: Bachelor’s Degree or equivalent combination of education and experience. Six years of dedicated experience in oncology clinical research budget development and negotiation and/or coverage analysis development. Experience working in research administration, a Contract Research Organization, pharma, biotech industry, academic medical center, or a clinical practice arena. Experience with HCPCS / CPT codes. Experience with Medicare regulations, guidelines, policies. Preferred education: PharmD, Bachelor of Science in Nursing, or Masters in a health-related field. Additional Information: Job Status: Full time, exempt Salary range $130,977 - $161,219 City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . 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Boston, Massachusetts, United States; San Francisco, California, United States; Santa Monica, California, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "technicalSkills" : "Computer science, Business-related discipline", "professionalSkills" : [ "Financial forecasts", "Financial reporting", "Business process improvement", "Systems expertise", "Compliance reporting", "Financial processes", "Financial systems", "Tax group", "Contract negotiation", "Purchase orders", "Quality metrics", "Financial data analysis", "Resource usage management", "Clinical trial spend", "Information requests", "Financial projects", "Budget reporting", "Financial reports" ], "hardSkillsList" : [ "Data capture systems", "Clinical process", "Good clinical practice", "Financial data analysis", "Resource management" ], "softSkillsList" : [ "Strategic thinking", "Analytical thinking", "Cultural awareness", "Attention to detail", "Problem-solving skills" ], "hardSkills" : [ { "name" : "Data capture systems", "level" : "intermediate" }, { "name" : "Clinical process", "level" : "intermediate" }, { "name" : "Good clinical practice", "level" : "intermediate" }, { "name" : "Financial data analysis", "level" : "intermediate" }, { "name" : "Resource management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Strategic thinking" }, { "name" : "Analytical thinking" }, { "name" : "Cultural awareness" }, { "name" : "Attention to detail" }, { "name" : "Problem-solving skills" } ], "majorSkills" : "Finance control, Financial reporting, Clinical operations, Systems expertise", "majorSkillsList" : [ "Finance control", "Financial reporting", "Clinical operations", "Systems expertise" ], "coreResponsibilities" : "Provide financial forecasts, Ensure accuracy of financial reporting, Provide systems and information expertise, Assist in continuous improvement, Support and implement strategy for clinical systems, Ensure financial processes are understood, Fulfil accountabilities of SOX, Ensure users understand ACCORD/ABACUS, Provide ACCORD/ABACUS training, Participate in ACCORD/ABACUS user forums, Ensure correct LSADs input, Manage and maintain monthly ACCORD/ABACUS, Manage and maintain SAP, Manage and maintain Finance Month End processes, Ensure global and local financial systems are utilized, Partner with local finance department, Partner with tax group, Provide support to contract negotiation, Provide support to purchase order finalization, Implement quality metrics, Analyze financial data, Analyze resource usage, Manage resource usage, Manage and analyze monthly ACCORD submissions, Analyze clinical trial spend, Report clinical trial spend, Collect data for local information requests, Prepare data for local information requests, Global representation on systems projects, Local representation on systems projects, Global representation on financial projects, Local representation on financial projects, Conduct activities consistent with Company values, Complete required training, Report potential issues of noncompliance, Implement proper controls, Ensure readiness for ABACUS rollout, Look for best practices, Develop budgets, Develop budget reporting, Develop financial reports, Develop financial analysis, Escalate systematic quality issues, Escalate serious quality issues, Escalate data privacy breaches, Escalate CSP compliance issues, Escalate ICH-GCP compliance issues", "teamCollaboration" : "Liaising with LDO Finance Director; Liaising with local/regional Finance Department; Partner with local finance department; Partner with tax group", "projectManagementSkills" : [ "Systems projects", "Financial projects" ], "domainKnowledge" : "Clinical operations; ICH-GCP; Local regulations; Good clinical practice", "domainList" : [ "clinical-operations", "ich-gcp", "local-regulations", "good-clinical-practice" ], "domainSpecificKnowledge" : [ "Clinical operations", "ICH-GCP", "Local regulations", "Good clinical practice" ], "toolProficiency" : [ "CTMS", "ABACUS", "Rave", "ACCORD", "SAP" ], "communicationSkills" : "Excellent communication skills", "problemSolvingSkills" : "Problem-solving skills", "outcomesObjectives" : "Meet monthly reporting timelines; Deliver status reports; Deliver quality clinical trials", "qualificationsBasic" : "College diploma/university degree, More than 5 years of experience in a clinical trial environment, Good understanding of Finance control, Knowledge of financial reporting, Good understanding of IT and data capture systems, Sound knowledge of clinical process, Good clinical practice knowledge", "qualificationsPreferred" : "Ability to work in an environment of remote collaborators, Manages change with a positive approach, Ability to look for and champion more efficient methods, Ability to understand the impact of technology on projects, Develop computer skills, Use and develop computer skills", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "**Job Summary** The main purpose of this role is to support the delivery of the Global Clinical R&D portfolio and clinical projects. The delivery of clinical projects should be to agreed productivity, within agreed budget and to inspection ready quality standards. The Finance Director will lead business and process improvement projects to drive better business outcomes and implement agreed improvements across the organization. The Finance Director will support Global CTCO SMM with systems and finance support to meeting monthly reporting timelines and to plan, control and follow-up on business information (e.g. CTMS, ABACUS) in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations. The Finance Director will support all clinical projects in Global CTCO SMM providing access to business & finance information and liaising with LDO Finance Director and local/regional Finance Department as well as gather and interpret insight on CTCO SM&M organization. In addition to Gaithersburg, MD this role can be based in Boston, MA, San Francisco, CA, or Santa Monica, CA, offering flexibility across these locations. **You will:** * Provide CTCO SMM - global with support of financial forecasts and other resource related processes in line with requirement of Finance Director. * Ensure accuracy of all financial reporting both internal and external costs. * Provides a high level of application and information system expertise to the business to maximize reliability, productivity, speed, quality and cost containment. * Assist in the continuous improvement of CTCO SMM in terms of compliance and key performance indicators. This includes reviewing performance and resource data to be able to deliver status reports. * Support and implement strategy for efficient and effective use of all clinical systems (CTMS, Rave, ABACUS) in CTCO SMM including access management, end user support, compliance reporting, conduct training and testing as needed. * Ensure financial processes and practices are understood and adhered to within the department. * Fulfil accountabilities of SOX as needed. * Ensure that all users understand how ACCORD/ABACUS operates. Provide ACCORD/ABACUS training and give appropriate first line support to local users. * Participate actively in the ACCORD/ABACUS user forums with suggestions and feedback on ACCORD/ABACUS/ process related questions * Ensure correct and up to date LSADs input into key systems ACCORD/ABACUS) especially subject fees. * Manage and maintain monthly ACCORD/ABACUS, SAP and Finance Month End processes. * Ensure global and local financial systems are utilized correctly through training of users and review of processes and data. * Partner with local finance department and tax group as necessary to ensure effective Scientific Research and Experimental Development submissions and audits. * Provide support to the negotiation and finalization of contracts and purchase orders as needed. * Implement and analyze quality metrics in relation to study process objectives with a specific focus on analysis of financial data and resource usage and management. * Management and analysis of monthly ACCORD submissions. * Analysis of clinical trial spend and reporting. * Data collection and preparation for local information requests (studies, investments by phase, by TA, etc.). * Global representation/participation and local representation/participation on systems and financial projects. * Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies relevant to the role. Complete all required training on the AZ Code of Conduct and supporting Policies on time. Report potential issues of noncompliance. * Implement proper controls performed by LSADs and Country Heads, including attestation control and balance sheet review control. * Ensuring readiness for the rollout of new ABACUS system. * Actively look for best practices in countries that could be shared and developed with others. * Develop budgets, budget reporting, other financial reports and analysis. * Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, CSP or ICH-GCP compliance issues to Local Management and/or CQM as required. **You have** : * College diploma/university degree in computer science or business-related discipline. * More than 5 years of experience in a clinical trial environment. * Good understanding of Finance control in the business setting and knowledge of financial reporting. * Good understanding and keen interest in IT and data capture systems * Strong strategic and analytical thinking. * Good cultural awareness. * Ability to develop advanced computer skills to increase efficiency in day-to-day tasks. * Ability to train others on systems processes. * Display excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting priorities. * Sound knowledge or clinical process and good clinical practice. * Excellent communication, analytical and problem-solving skills. * Team oriented and flexible; ability to respond quickly to shifting demands and opportunities. **Desired skills:** * Ability to work in an environment of remote collaborators. * Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business. * Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time. * Good analytical and problem-solving skills. * Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines. * Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an enabled environment. **Benefits offered include:** A qualified retirement program [401(k) plan] Paid vacation, holidays, and paid leaves Health benefits including medical, prescription drug, dental, and vision coverage following the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. The annual base salary for this position ranges from $148,000 to $222,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). **Date Posted** 10-Jun-2026 **Closing Date** 09-Jul-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.", "summaryDescription" : "Finance Director, Cell Therapy Clinical Operations -SMM at Mission. Skills: Finance control, Financial reporting, Clinical operations, Systems expertise. Provide financial forecasts. Ensure accuracy of financial reporting", "postedDate" : "2026-06-11T05:05:05.010", "createdAt" : "2026-06-12T05:05:04.896", "lastUpdated" : "2026-06-14T23:45:52.994", "ingestTimestamp" : "2026-06-12T05:05:04.896", "mongoId" : "6a2af78274d8ee00a073d611", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/US---Gaithersburg---MD/Finance-Director--Cell-Therapy-Clinical-Operations--SMM_R-253947-2", "salaryAnnualMin" : 148000, "salaryAnnualMax" : 148000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Data capture systems", "Clinical process", "Good clinical practice", "Financial data analysis", "Resource management", "Strategic thinking", "Analytical thinking", "Cultural awareness", "Attention to detail", "Problem-solving skills", "Finance control", "Financial reporting", "Clinical operations", "Systems expertise", "Financial forecasts", "Business process improvement", "Compliance reporting", "Financial processes", "Financial systems", "Tax group", "Contract negotiation", "Purchase orders", "Quality metrics", "Resource usage management", "Clinical trial spend", "Information requests", "Financial projects", "Budget reporting", "Financial reports", "Systems projects", "ICH-GCP", "Local regulations", "CTMS", "ABACUS", "Rave", "ACCORD", "SAP" ], "skillCount" : 37, "jobCategory" : "finance", "seniorityLevel" : "executive", "dataQualityScore" : 1.0, "_score" : 731.98566, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Financial Services" }, { "id" : "6a30505ff292fd229ceefa30", "title" : "Senior Battery Engineer, Cell Performance", "company" : "Form Energy", "industry" : "Research & Development", "salary" : { "min" : 128662.0, "max" : 160807.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Somerville, MA", "locations" : [ "Somerville, MA" ], "timestamp" : "2026-06-16T10:12:28.383", "fingerprint" : "e7a61a75812c13f2b7e60ef468d0143b6b224c44e84cceb39e45ef7f733a4daa", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/FORMENERGY/cf18ec32-014a-49c4-bdf6-591166d6d276/application", "externalId" : "cf18ec32-014a-49c4-bdf6-591166d6d276", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Somerville", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3875968,-71.0994968" } ], "locationText" : "Somerville, Massachusetts, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Battery cell design, Battery cell testing, Battery cell manufacturing, Lithium-ion battery, Solid-state battery, Battery modeling, Battery simulation", "professionalSkills" : [ "System design", "Data analysis", "Project management" ], "hardSkillsList" : [ "Electrochemical principles", "Materials science", "Thermodynamics", "Statistical analysis" ], "hardSkills" : [ { "name" : "Electrochemical principles", "level" : "intermediate" }, { "name" : "Materials science", "level" : "intermediate" }, { "name" : "Thermodynamics", "level" : "intermediate" }, { "name" : "Statistical analysis", "level" : "intermediate" } ], "majorSkills" : "Battery cell engineering, Cell performance, Cell testing", "majorSkillsList" : [ "Battery cell engineering", "Cell performance", "Cell testing" ], "coreResponsibilities" : "Design battery cells, Develop battery cell testing protocols, Execute battery cell tests, Analyze battery cell performance data, Identify and resolve battery cell issues, Collaborate with manufacturing teams, Contribute to battery cell roadmap, Stay current with battery technology trends", "teamCollaboration" : "Cross-functional teams; Manufacturing engineers; Research scientists", "projectManagementSkills" : [ "Project planning", "Task prioritization", "Timeline management" ], "domainKnowledge" : "Battery electrochemistry; Battery materials; Battery manufacturing processes; Battery safety standards", "domainList" : [ "battery-electrochemistry", "battery-materials", "battery-manufacturing-processes", "battery-safety-standards" ], "domainSpecificKnowledge" : [ "Battery electrochemistry", "Battery materials", "Battery manufacturing processes", "Battery safety standards" ], "toolProficiency" : [ "Battery testing equipment", "Data analysis software", "Simulation software" ], "communicationSkills" : "Technical reports; Presentations", "documentationSkills" : "Test reports; Design specifications", "continuousLearning" : "Attend industry conferences; Read technical publications", "innovationCreativity" : "Develop novel cell designs; Improve cell performance", "problemSolvingSkills" : "Root cause analysis; Troubleshooting; Data-driven decisions", "outcomesObjectives" : "Improve cell energy density; Enhance cell cycle life; Reduce cell cost; Ensure cell safety and reliability", "qualificationsBasic" : "Bachelor's degree in engineering, 5+ years of experience in battery cell engineering, Experience with battery cell design, Experience with battery cell testing, Experience with battery cell manufacturing", "qualificationsPreferred" : "Master's degree or PhD in a relevant field, Experience with lithium-ion battery chemistries, Experience with solid-state battery technologies, Experience with battery modeling and simulation software", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Are you ready to build America’s energy future? Form Energy is an American manufacturing and energy technology company. We’re revolutionizing energy storage with cost-effective, multi-day technology designed to keep the electric grid secure and reliable, even during extended periods of stress. By strengthening the electric system and reimagining what’s possible, we’re giving clean energy a whole new form! In recent years, Form Energy has earned a number of accolades, including being named by TIME as a “Best Invention”, MIT Technology Review as a “Top Climate Tech Company To Watch”, and Fast Company as “One of the Next Big Things In Tech”. We are making rapid progress on our mission of delivering energy storage for a better world, and our team is growing just as rapidly to meet demand. We have signed contracts with leading electric utilities across the United States and production of our iron-air batteries is underway at our first high-volume manufacturing facility in West Virginia. Working for Form Energy is more than just a job, it’s a chance to be part of something extraordinary. And now - right as we significantly scale up battery manufacturing - might be the most exciting moment in the company’s history to join. We are assembling a team of highly talented and driven individuals across the country. Driven by our core values of humanity, excellence, and creativity, our team is determined to deliver on our mission and transform the energy landscape for the better. Feeling energized to make a meaningful impact on the world? Then keep reading - you’ve come to the right place. ROLE DESCRIPTION Form Energy is hiring a Battery Engineer to join our Cell Package Integration team. As a Battery Engineer on our team, you will design and execute experiments that connect component-level changes to cell-level outcomes, investigate root causes of performance variation, and work closely with electrode, electrolyte, and manufacturing teams to identify and integrate cell improvements across cost, performance, and lifetime. This is a practical technical role for someone with solid electrochemical knowledge and a collaborative approach to cross-functional problem-solving. You'll be joining a team building something that has never been built before, with a clear shot at reshaping how the world stores energy with our breakthrough technology. The level of this position is flexible upwards based on experience. Relocation assistance is available. WHAT YOU'LL DO: - Design, execute, and analyze cell-level experiments to characterize electrochemical performance, qualify cell package designs, and identify limiting factors or failure modes - Champion safety as you carry out electrochemical testing in benchtop and lab-scale test vehicles in collaboration with the test execution team - Investigate performance failures and degradation modes using root cause analysis methods, translating findings into corrective actions and design improvements - Lead continuous improvement in our battery testing program — standardizing protocols and ensuring test procedures reflect the product-relevant operational space - Conduct durability and entitlement testing on prototype cell packages to develop data-backed design specifications and inform DFMEAs - Partner with electrode, electrolyte, and manufacturing teams to identify improvement opportunities, coordinate cell builds, and close performance gaps across cost, performance, and lifetime WHAT YOU'LL BRING: - Bachelor or Master’s degree in Chemical Engineering, Chemistry, Electrochemistry, Materials Science, or a related field with 4+ years of relevant industry or research experience OR PhD with relevant industry or research experience - Hands-on practical experience with electrochemical systems and electrochemical device data interpretation, particularly in deployed or market-ready products - Expertise with failure prediction and investigation methods, such as Root Cause Analysis and Failure Modes and Effects Analysis - Excellent communication and organizational skills, including working with teams in different locations on shared objectives - Statistical experimental design, such as fractional factorial designs, and linear regression analysis #LI-Onsite #LI-LN1 Humanity is a cornerstone of Form Energy’s culture, and we make sure our compensation and benefits reflect that. Form Energy offers competitive salaries, stock options, and a holistic benefits package to ensure all employees have what they need to thrive while working here. When it comes to you and your family’s health, we cover 100% of medical, dental, and vision premiums for full-time employees - and 80% of healthcare premiums for dependents. This starts from day one. We also offer at least 12 weeks of paid leave for new parents (up to 20 weeks for birthing parents), and generous vacation policies to give employees time to recharge when needed. To build America’s energy future, we need everyone at the table. We are proud to be an equal opportunity employer, and encourage candidates from all backgrounds to apply to our open jobs. If you may require reasonable accommodations to participate in our interview process, please contact accommodations@formenergy.com. Requests for accommodations will be treated with discretion. Form Energy is committed to maintaining the privacy of our applicants. Please be aware that we will never solicit sensitive personal information such as Social Security numbers or bank account details during the recruiting or hiring process.", "summaryDescription" : "Senior Battery Engineer, Cell Performance at Form Energy. Skills: Battery cell engineering, Cell performance, Cell testing. Design battery cells. 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Enhance battery cell reliability; Reduce battery cell costs", "qualificationsBasic" : "Bachelor's degree in engineering, 5+ years of experience in battery cell engineering, Experience with battery cell design, Experience with battery cell testing, Experience with battery cell manufacturing", "qualificationsPreferred" : "Master's degree or PhD in a relevant field, Experience with lithium-ion battery chemistries, Experience with solid-state battery technologies, Experience with battery modeling and simulation, Experience with battery safety standards", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Are you ready to build America’s energy future? Form Energy is an American manufacturing and energy technology company. We’re revolutionizing energy storage with cost-effective, multi-day technology designed to keep the electric grid secure and reliable, even during extended periods of stress. By strengthening the electric system and reimagining what’s possible, we’re giving clean energy a whole new form! In recent years, Form Energy has earned a number of accolades, including being named by TIME as a “Best Invention”, MIT Technology Review as a “Top Climate Tech Company To Watch”, and Fast Company as “One of the Next Big Things In Tech”. We are making rapid progress on our mission of delivering energy storage for a better world, and our team is growing just as rapidly to meet demand. We have signed contracts with leading electric utilities across the United States and production of our iron-air batteries is underway at our first high-volume manufacturing facility in West Virginia. Working for Form Energy is more than just a job, it’s a chance to be part of something extraordinary. And now - right as we significantly scale up battery manufacturing - might be the most exciting moment in the company’s history to join. We are assembling a team of highly talented and driven individuals across the country. Driven by our core values of humanity, excellence, and creativity, our team is determined to deliver on our mission and transform the energy landscape for the better. Feeling energized to make a meaningful impact on the world? Then keep reading - you’ve come to the right place. ROLE DESCRIPTION Form Energy is hiring a Battery Engineer to join our Cell Package Integration team. As a Battery Engineer on our team, you will design and execute experiments that connect component-level changes to cell-level outcomes, investigate root causes of performance variation, and work closely with electrode, electrolyte, and manufacturing teams to identify and integrate cell improvements across cost, performance, and lifetime. This is a practical technical role for someone with solid electrochemical knowledge and a collaborative approach to cross-functional problem-solving. You'll be joining a team building something that has never been built before, with a clear shot at reshaping how the world stores energy with our breakthrough technology. The level of this position is flexible upwards based on experience. Relocation assistance is available. WHAT YOU'LL DO: - Design, execute, and analyze cell-level experiments to characterize electrochemical performance, qualify cell package designs, and identify limiting factors or failure modes - Champion safety as you carry out electrochemical testing in benchtop and lab-scale test vehicles in collaboration with the test execution team - Investigate performance failures and degradation modes using root cause analysis methods, translating findings into corrective actions and design improvements - Lead continuous improvement in our battery testing program — standardizing protocols and ensuring test procedures reflect the product-relevant operational space - Conduct durability and entitlement testing on prototype cell packages to develop data-backed design specifications and inform DFMEAs - Partner with electrode, electrolyte, and manufacturing teams to identify improvement opportunities, coordinate cell builds, and close performance gaps across cost, performance, and lifetime WHAT YOU'LL BRING: - Bachelor or Master’s degree in Chemical Engineering, Chemistry, Electrochemistry, Materials Science, or a related field with 4+ years of relevant industry or research experience OR PhD with relevant industry or research experience - Hands-on practical experience with electrochemical systems and electrochemical device data interpretation, particularly in deployed or market-ready products - Expertise with failure prediction and investigation methods, such as Root Cause Analysis and Failure Modes and Effects Analysis - Excellent communication and organizational skills, including working with teams in different locations on shared objectives - Statistical experimental design, such as fractional factorial designs, and linear regression analysis #LI-Onsite #LI-LN1 Humanity is a cornerstone of Form Energy’s culture, and we make sure our compensation and benefits reflect that. Form Energy offers competitive salaries, stock options, and a holistic benefits package to ensure all employees have what they need to thrive while working here. When it comes to you and your family’s health, we cover 100% of medical, dental, and vision premiums for full-time employees - and 80% of healthcare premiums for dependents. This starts from day one. We also offer at least 12 weeks of paid leave for new parents (up to 20 weeks for birthing parents), and generous vacation policies to give employees time to recharge when needed. To build America’s energy future, we need everyone at the table. We are proud to be an equal opportunity employer, and encourage candidates from all backgrounds to apply to our open jobs. If you may require reasonable accommodations to participate in our interview process, please contact accommodations@formenergy.com. Requests for accommodations will be treated with discretion. Form Energy is committed to maintaining the privacy of our applicants. 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City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. This full-time remote position entails ensuring data integrity for various research studies. Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data. You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research. As a successful candidate, you will: Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations. Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information. Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution. Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements. Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work. Qualifications - External Qualifications - External Qualifications - External Your qualifications should include: Bachelor’s Degree, relevant experience may substitute for degree. At least two years of experience related to the conduct of oncology clinical trials. Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Clinical Trials Data Coord at City of Hope. Skills: Data science, Data engineering, ML/AI, Business intelligence, Analytics engineering. Ensure data integrity. Complete CRFs", "createdAt" : "2026-06-14T00:49:20.231", "lastUpdated" : "2026-06-15T08:24:18.362", "ingestTimestamp" : "2026-06-14T00:49:20.231", "mongoId" : "69dde45b2beec4dd3d9a3ed3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Statistical methods", "ML frameworks", "BI platforms", "Cloud data stacks", "Modelling skills", "Quantitative analysis", "Data science", "Data engineering", "ML/AI", "Business intelligence", "Analytics engineering", "Data abstraction", "Query resolution", "Data integrity", "Electronic records", "Patient information", "Good Clinical Practices", "FDA regulations", "NIH guidelines", "HIPAA regulations", "Clinical research", "Study protocols", "GCP Professional Data Engineer", "AWS Data Analytics", "Databricks Certified", "Dbt Certified", "CTMS" ], "skillCount" : 27, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Junior", "dataQualityScore" : 0.7777778, "_score" : 723.1992, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3073e2f292fd229c0043ba", "title" : "Junior Trial Attorney", "company" : "Abramson Labor Group", "industry" : "Legal Services", "salary" : { "min" : 150000.0, "max" : 200000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Burbank, CA, United States", "locations" : [ "Burbank", "CA", "United States" ], "certifications" : [ "Bar Admission" ], "timestamp" : "2026-06-16T13:34:07.771", "fingerprint" : "d1bf6a5a55a45b1154490f026a9a09b8bd0514427e50b13802db5f5c385c63e6", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/AbramsonLaborGroup/3743990013632006--junior-trial-attorney-hybrid-schedule-", "externalId" : "3743990013632006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Burbank", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "34.1812089,-118.3072010" } ], "locationText" : "Burbank, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Juris Doctor", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Case management", "Legal strategy", "Client advising", "Business generation" ], "hardSkillsList" : [ "Legal research", "Drafting pleadings", "Interviewing witnesses", "Gathering evidence", "Negotiating settlements", "Analyzing documents", "Managing budgets" ], "hardSkills" : [ { "name" : "Legal research", "level" : "intermediate" }, { "name" : "Drafting pleadings", "level" : "intermediate" }, { "name" : "Interviewing witnesses", "level" : "intermediate" }, { "name" : "Gathering evidence", "level" : "intermediate" }, { "name" : "Negotiating settlements", "level" : "intermediate" }, { "name" : "Analyzing documents", "level" : "intermediate" }, { "name" : "Managing budgets", "level" : "intermediate" } ], "majorSkills" : "Trial advocacy, Employment law, Case progression", "majorSkillsList" : [ "Trial advocacy", "Employment law", "Case progression" ], "coreResponsibilities" : "Represent clients in court, Conduct hearings, Participate in arbitrations, Attend mediations, Develop case strategies, Present arguments to judges, Present arguments to juries, Conduct legal research, Draft pleadings, Draft motions, Draft briefs, Interview witnesses, Gather evidence, Prepare for trial, Negotiate settlements, Negotiate plea agreements, Provide legal advice, Guide clients on litigation, Manage support staff, Review employment law documents, Analyze employment law documents, Review contracts, Analyze contracts, Monitor court deadlines, Monitor procedural requirements, Participate in client development, Participate in business generation, Maintain case files, Maintain documentation, Develop litigation budgets, Implement litigation budgets, Coordinate expert witnesses, Coordinate consultants", "teamCollaboration" : "Work with legal teams; Work with paralegals; Work with investigators; Work with litigation associates", "projectManagementSkills" : [ "Case management", "Meet strict deadlines" ], "domainKnowledge" : "Employment law; Workers' compensation; Discrimination law; Harassment law; Wrongful termination; Wage disputes; Workplace injuries; Procedural rules", "domainList" : [ "employment-law", "workers-compensation", "discrimination-law", "harassment-law", "wrongful-termination", "wage-disputes", "workplace-injuries", "procedural-rules" ], "domainSpecificKnowledge" : [ "Employment law", "Workers' compensation", "Discrimination law", "Harassment law", "Wrongful termination", "Wage disputes", "Workplace injuries", "Procedural rules" ], "communicationSkills" : "Present arguments", "documentationSkills" : "Maintain case files; Maintain documentation", "continuousLearning" : "Continuing legal education (CLE)", "problemSolvingSkills" : "Legal analysis", "outcomesObjectives" : "Achieve favorable outcomes", "qualificationsBasic" : "Juris Doctor (J.D.), Licensed to practice law, 2-3 years litigation experience, Trial experience", "qualificationsPreferred" : "Familiarity with procedural rules", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Abramson Labor Group is a leading employment and workers' compensation law firm dedicated to advocating for employees' rights. Based in Burbank, CA, we are determined in representing workers who have faced discrimination, harassment, wrongful termination, wage disputes, and workplace injuries. Our team is committed to providing top-tier legal representation with a client-focused approach, ensuring that every case receives the attention and expertise it deserves. At Abramson Labor Group, we foster a dynamic and collaborative work environment where professionals can grow while making a meaningful impact in the lives of our clients. If you are passionate about employment law and workers' rights, we invite you to join our dedicated team. We are seeking a detail-oriented and motivated individual to join our legal team as a Junior Trial Attorney. The successful candidate will play a pivotal role in managing a docket of employment law cases, ensuring efficient case progression, and achieving favorable outcomes for our clients. Key Responsibilities * Represent clients in court trials, hearings, arbitrations, and mediations. * Develop case strategies and present arguments before judges and juries. * Conduct legal research and draft pleadings, motions, and briefs. * Interview witnesses, gather evidence, and prepare for trial. * Negotiate settlements and plea agreements when appropriate. * Provide legal advice and guidance to clients on litigation matters. * Work collaboratively with legal teams, paralegals, and investigators. * Stay up to date with changes in laws, regulations, and legal precedents. * Manage and supervis support staff. * Review and analyze complex employment law documents and contracts. * Monitor compliance with court deadlines and procedural requirements. * Participate in client development and business generation activities. * Maintain detailed case files and documentation. * Develop and implement litigation budgets. * Coordinate with expert witnesses and consultants. ## Qualifications Education: Juris Doctor (J.D.) from an accredited law school. Bar Admission: Licensed to practice law in the relevant jurisdiction(s). Experience: * 2-3 years of litigation experience * Ideally, the candidate will have trial experience. * Strong background in procedural rules (e.g., Rule 23 of the Federal Rules of Civil Procedure). Skills: * Ability to manage multiple cases and meet strict deadlines. * Project management and ability to work as a team player with litigation associates. ## Additional Information What We Offer: * Competitive salary and performance-based bonuses. * Comprehensive benefits package, including health insurance, retirement plans, and unlimited paid time off (PTO). * Opportunities for professional development and continuing legal education (CLE). * A supportive work environment dedicated to teamwork, integrity, and excellence in client service. Department Civil Litigation Employment Type Full Time Location Burbank, CA Workplace type Hybrid Compensation $150,000 - $200,000 / year commensurate with experience #ZR", "summaryDescription" : "Junior Trial Attorney at Abramson Labor Group. Skills: Trial advocacy, Employment law, Case progression. Represent clients in court. 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Work with paralegals; Work with investigators", "domainKnowledge" : "Employment law; Workers' rights; Discrimination law; Harassment law; Wrongful termination; Wage disputes; Workplace injuries; Procedural rules", "domainList" : [ "employment-law", "workers-rights", "discrimination-law", "harassment-law", "wrongful-termination", "wage-disputes", "workplace-injuries", "procedural-rules" ], "domainSpecificKnowledge" : [ "Employment law", "Workers' rights", "Discrimination law", "Harassment law", "Wrongful termination", "Wage disputes", "Workplace injuries", "Procedural rules" ], "documentationSkills" : "Case file maintenance", "continuousLearning" : "Continuing legal education (CLE)", "outcomesObjectives" : "Achieve favorable outcomes for clients", "qualificationsBasic" : "Juris Doctor (J.D.), Licensed to practice law, 2 years litigation experience, Must reside in California", "qualificationsPreferred" : "Trial experience, Background in procedural rules", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Abramson Labor Group is a leading employment and workers' compensation law firm dedicated to advocating for employees' rights. Based in Burbank, CA, we are determined in representing workers who have faced discrimination, harassment, wrongful termination, wage disputes, and workplace injuries. Our team is committed to providing top-tier legal representation with a client-focused approach, ensuring that every case receives the attention and expertise it deserves. At Abramson Labor Group, we foster a dynamic and collaborative work environment where professionals can grow while making a meaningful impact in the lives of our clients. If you are passionate about employment law and workers' rights, we invite you to join our dedicated team. We are seeking a detail-oriented and motivated individual to join our legal team as a Trial Attorney. The successful candidate will play a pivotal role in managing a docket of employment law cases, ensuring efficient case progression, and achieving favorable outcomes for our clients. Key Responsibilities * Represent clients in court trials, hearings, arbitrations, and mediations. * Develop case strategies and present arguments before judges and juries. * Conduct legal research and draft pleadings, motions, and briefs. * Interview witnesses, gather evidence, and prepare for trial. * Negotiate settlements and plea agreements when appropriate. * Provide legal advice and guidance to clients on litigation matters. * Work collaboratively with legal teams, paralegals, and investigators. * Stay up to date with changes in laws, regulations, and legal precedents. * Manage and supervise junior attorneys and support staff. * Review and analyze complex employment law documents and contracts. * Monitor compliance with court deadlines and procedural requirements. * Participate in client development and business generation activities. * Maintain detailed case files and documentation. * Develop and implement litigation budgets. * Coordinate with expert witnesses and consultants. ## Qualifications Education: Juris Doctor (J.D.) from an accredited law school. Bar Admission: Licensed to practice law in the relevant jurisdiction(s). Experience: * 2 years of litigation experience * Ideally, the candidate will have trial experience. * Strong background in procedural rules (e.g., Rule 23 of the Federal Rules of Civil Procedure). Skills: * Ability to manage multiple cases and meet strict deadlines. * Project management and ability to work as a team player with litigation associates. ## Additional Information What We Offer: * Competitive salary and performance-based bonuses. * Comprehensive benefits package, including health insurance, retirement plans, and unlimited paid time off (PTO). * Opportunities for professional development and continuing legal education (CLE). * A supportive work environment dedicated to teamwork, integrity, and excellence in client service. Department Civil Litigation Employment Type Full Time Location Burbank, CA Workplace type Remote - must reside in California Compensation $180,000 - $250,000 / year commensurate with experience #ZR", "summaryDescription" : "Junior Trial Attorney at Abramson Labor Group. Skills: Employment law, Workers' compensation, Litigation, Trial advocacy. Represent clients in court. 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D. )", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Legal writing", "Legal research", "Analytical skills", "Negotiation", "Oral advocacy", "Project management", "Team leadership" ], "hardSkillsList" : [ "Class action litigation" ], "hardSkills" : [ { "name" : "Class action litigation", "level" : "intermediate" } ], "majorSkills" : "Employment law, Class action litigation, Trial advocacy", "majorSkillsList" : [ "Employment law", "Class action litigation", "Trial advocacy" ], "coreResponsibilities" : "Represent clients in court, Represent clients in hearings, Represent clients in arbitrations, Represent clients in mediations, Develop case strategies, Present arguments before judges, Present arguments before juries, Conduct legal research, Draft pleadings, Draft motions, Draft briefs, Interview witnesses, Gather evidence, Prepare for trial, Negotiate settlements, Negotiate plea agreements, Provide legal advice, Provide guidance to clients, Work collaboratively with legal teams, Work collaboratively with paralegals, Work collaboratively with investigators, Stay up to date with laws, Stay up to date with regulations, Stay up to date with legal precedents, Manage junior attorneys, Supervise junior attorneys, Manage support staff, Supervise support staff, Review employment law documents, Analyze employment law documents, Review employment law contracts, Analyze employment law contracts, Monitor compliance with court deadlines, Monitor compliance with procedural requirements, Participate in client development, Participate in business generation, Maintain detailed case files, Maintain documentation, Develop litigation budgets, Implement litigation budgets, Coordinate with expert witnesses, Coordinate with consultants", "teamCollaboration" : "Legal teams; Paralegals; Investigators; Support staff", "domainKnowledge" : "Employment law; Class actions; Procedural rules; Rule 23; Wage and Hour law", "domainList" : [ "employment-law", "class-actions", "procedural-rules", "rule-23", "wage-and-hour-law" ], "domainSpecificKnowledge" : [ "Employment law", "Class actions", "Procedural rules", "Rule 23", "Wage and Hour law" ], "toolProficiency" : [ "Litigation technology", "Document management tools", "E-discovery platforms", "Legal research databases" ], "communicationSkills" : "Oral advocacy", "documentationSkills" : "Case files documentation", "continuousLearning" : "Continuing legal education", "problemSolvingSkills" : "Analytical skills", "specialRequirements" : "Must reside in California", "outcomesObjectives" : "Achieve favorable outcomes", "qualificationsBasic" : "Juris Doctor (J. D. ), Licensed to practice law, 5+ years litigation experience, Trial experience, Depositions experience, Motions experience, Courtroom advocacy experience, Procedural rules experience, Class action settlements experience, Class certification motions experience", "qualificationsPreferred" : "Experience handling large-scale settlements, Mass tort litigation experience, Consumer protection background, Securities fraud background, Employment law background, Antitrust cases background, Federal court litigation experience, Publication record, Speaking engagements experience", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "At Abramson Labor Group, we're not just committed to defending employee rights—we're passionate about it. Whether you're up against a small business or a corporate giant, our highly skilled team of attorneys and legal professionals are ready to fight for you. Headquartered in vibrant Burbank, California, we focus on exclusively protecting employees throughout the entire state of beautiful California. Our dedicated attorneys, paralegals and legal assistants work tirelessly to secure the justice you deserve in all workplace disputes. We pride ourselves on delivering top-notch solutions with integrity, efficiency, and professionalism. Choose Abramson Labor Group and let us champion your cause with unwavering dedication. We are seeking a detail-oriented and motivated individual to join our legal team as a Trial Attorney (Wage & Hour). The successful candidate will play a pivotal role in managing a docket of employment law cases, ensuring efficient case progression, and achieving favorable outcomes for our clients. Key Responsibilities * Represent clients in court trials, hearings, arbitrations, and mediations. * Develop case strategies and present arguments before judges and juries. * Conduct legal research and draft pleadings, motions, and briefs. * Interview witnesses, gather evidence, and prepare for trial. * Negotiate settlements and plea agreements when appropriate. * Provide legal advice and guidance to clients on litigation matters. * Work collaboratively with legal teams, paralegals, and investigators. * Stay up to date with changes in laws, regulations, and legal precedents. * Manage and supervise junior attorneys and support staff. * Review and analyze complex employment law documents and contracts. * Monitor compliance with court deadlines and procedural requirements. * Participate in client development and business generation activities. * Maintain detailed case files and documentation. * Develop and implement litigation budgets. * Coordinate with expert witnesses and consultants. ## Qualifications Education: Juris Doctor (J.D.) from an accredited law school. Bar Admission: Licensed to practice law in the relevant jurisdiction(s). Experience: * 5+ years of litigation experience, preferably in class actions or complex civil litigation. * Trial experience, including depositions, motions, and courtroom advocacy. * Strong background in procedural rules governing class actions (e.g., Rule 23 of the Federal Rules of Civil Procedure). * Demonstrated experience in managing multi-million dollar class action settlements. * Track record of successful class certification motions. Skills: * Exceptional legal writing, research, and analytical skills. * Strong negotiation and oral advocacy abilities. * Ability to manage multiple cases and meet strict deadlines. * Proficiency in litigation technology and document management tools. * Advanced knowledge of e-discovery platforms and legal research databases. * Superior project management and team leadership capabilities. Preferred Qualifications: * Experience handling large-scale settlements or mass tort litigation. * Background in consumer protection, securities fraud, employment law, or antitrust cases. * Strong network and reputation in the legal community for class action litigation. * Advanced degree in Labor Law, Employment Law, or related field. * Federal court litigation experience. * Publication record in legal journals or speaking engagements at industry conferences. ## Additional Information What We Offer: * Competitive salary and performance-based bonuses. * Comprehensive benefits package, including health insurance, retirement plans, and unlimited paid time off (PTO). * Opportunities for professional development and continuing legal education (CLE). * A supportive work environment dedicated to teamwork, integrity, and excellence in client service. Department Civil Litigation Employment Type Full Time Location Burbank, CA Workplace type Remote Compensation $200,000 - $300,000 / year #ZR", "summaryDescription" : "Trial Attorney (Remote) at Abramson Labor Group. Skills: Employment law, Class action litigation, Trial advocacy. Represent clients in court. Represent clients in hearings", "postedDate" : "2026-06-15T21:26:55.000", "createdAt" : "2026-06-16T01:36:00.517", "lastUpdated" : "2026-06-16T14:56:59.023", "ingestTimestamp" : "2026-06-16T01:36:00.517", "mongoId" : "6a3073e2f292fd229c0043bc", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 200000, "salaryAnnualMax" : 300000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Class action litigation", "Employment law", "Trial advocacy", "Legal writing", "Legal research", "Analytical skills", "Negotiation", "Oral advocacy", "Project management", "Team leadership", "Class actions", "Procedural rules", "Rule 23", "Wage and Hour law", "Bar Admission", "Litigation technology", "Document management tools", "E-discovery platforms", "Legal research databases" ], "skillCount" : 19, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "_score" : 716.22363, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Legal", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305e6cf292fd229cf70716", "title" : "Lead Data Manager for Clinical Trials", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 125000.0, "max" : 175000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Data Manager in the Biotech industry in Mississauga, Canada, adjusted for seniority and company size." }, "location" : "Mississauga, ON, Canada", "locations" : [ "Mississauga", "ON", "Canada" ], "timestamp" : "2026-06-16T12:27:18.148", "fingerprint" : "59562c3e563210e83b94649065b46c42fee0a625104373527116857356c566e1", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000131984439-lead-data-manager-for-clinical-trials", "externalId" : "744000131984439", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Mississauga", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.5884727,-79.6436580" } ], "locationText" : "Mississauga, Ontario, Canada", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "technicalSkills" : "EDC systems", "professionalSkills" : [ "Data management", "Clinical data management", "Project management" ], "hardSkillsList" : [ "Data validation", "Data entry", "Database edits", "Medical data coding" ], "hardSkills" : [ { "name" : "Data validation", "level" : "intermediate" }, { "name" : "Data entry", "level" : "intermediate" }, { "name" : "Database edits", "level" : "intermediate" }, { "name" : "Medical data coding", "level" : "intermediate" } ], "majorSkills" : "Data management, Clinical trials", "majorSkillsList" : [ "Data management", "Clinical trials" ], "coreResponsibilities" : "Coordinate data management activities, Develop EDC, Collect data, Clean data, Reconcile data, Lock database, Generate final Data Management deliverables, Review study documents, Develop Data Management plan, Develop project-specific guidelines, Review project-specific guidelines, Perform user acceptance testing, Develop Data Validation Plan, Develop Edit Check Specifications, Coordinate data entry, Supervise data entry, Provide feedback to data entry personnel, Inspect data, Review data discrepancies, Resolve data discrepancies, Generate queries, Resolve queries, Provide feedback to clinical trial teams, Handle non-CRF electronic data, Receive non-CRF electronic data, Archive non-CRF electronic data, Load non-CRF electronic data, Review non-CRF electronic data reconciliation issues, Resolve non-CRF electronic data reconciliation issues, Provide feedback to vendors, Perform database edits, Perform manual CRF review, Lock clinical database, Coordinate CRF processing, Supervise CRF processing, Dispatch CRFs, Archive CRFs, Coordinate query processing, Supervise query processing, Dispatch queries, Archive queries, Input into design of CRFs, Design CRFs for accuracy, Ensure adherence to protocol, Develop CRF completion guidelines, Code medical data, Review coding listings, Perform SAE reconciliation, Review electronic data transfer specifications, Approve electronic data transfer specifications, Liaise with Document Center, Maintain TMF, Maintain eTMF, Perform Database QC checks, Document Database QC checks, Prepare for audits, Attend audits, Prepare for inspections, Attend inspections, Follow up on audit findings, Resolve audit findings, Train Assistant Data Managers, Provide project-specific training, Train investigators on CRF completion, Train clinical team on CRF completion, Prepare Investigator Meetings, Attend Investigator Meetings, Prepare for client meetings, Attend client meetings, Prepare for vendor teleconferences, Attend vendor teleconferences", "teamCollaboration" : "Project teams; Company departments; Clients; Vendors; Clinical teams", "projectManagementSkills" : [ "Project data management" ], "domainKnowledge" : "Clinical trials; EDC systems", "domainList" : [ "clinical-trials", "edc-systems" ], "domainSpecificKnowledge" : [ "Clinical trials", "EDC systems" ], "toolProficiency" : [ "Medidata Rave", "Oracle Inform" ], "communicationSkills" : "Client communication; Vendor communication", "documentationSkills" : "Study documents review; Data Management plan development; CRF completion guidelines development", "problemSolvingSkills" : "Data discrepancy resolution; Query resolution", "outcomesObjectives" : "Database Lock; Final integrated database development; Generation of final Data Management deliverables", "qualificationsBasic" : "College or University degree or equivalent combination of training and experience, At least 3 years of experience of full scope of data management responsibilities in global EDC studies, At least 2 years of experience using CDM/EDC systems", "qualificationsPreferred" : "Project data management experience is a plus, Medidata Rave or Oracle Inform preferable", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "We’re over 3,200+ strong across the globe. We’re scientists, strategists, creatives, and innovators. We value individual brilliance and build a strong foundation for teamwork across all our business. We love the challenge of our industry. We’re changing lives and redefining success every step of the way. The Lead Data Manager will be responsible for all data management activities in large, complex studies under general supervision, or working under minimal supervision on data management activities for small to medium sized projects. Communication * Primary communication point for project teams and company departments with regard to clinical data management * Communication line for clients/vendors for all data management aspects of clinical projects and clinical data management reporting Data Management * Coordination of data management activities within clinical projects related to EDC development, data collection, cleaning, reconciliation, Database Lock, development of final integrated database and generation of final Data Management deliverables. * Primary responsibility for clinical data management activities within clinical projects, including, but not limited to: * Study documents review * Data Management plan and other project-specific guidelines and instructions development and review * Co-ordinate/perform user acceptance testing * Development of Data Validation Plan/Edit Check Specifications * Data entry coordination and supervision, feedback to data entry personnel regarding quality of data entry and other data entry issues * Data validation, including automatic and manual data inspections, data discrepancies/deficiencies review and resolution, query generation and resolution, feedback to clinical trial teams regarding quality of data * Non-CRF electronic data handling (receiving, archiving, loading into study database, review and resolution of reconciliation issues, feedback to vendors regarding quality of data and other issues) * Database edits (paper CRF studies) * Manual CRF review (non-medical checks) * Clinical database lock * Coordination and supervision of processing, dispatch and archiving of CRFs/queries * Input into design of CRFs and other data collection forms; review Case Report Form design for accuracy and adherence to protocol * Development of CRF completion guidelines * Coding medical data with coding dictionaries and coding listings review (Lead DMs with medical/biology background, additional training required) * SAE reconciliation * Electronic data transfer (import/export) specifications review and approval Document Management * Liaison with Document Center with regard to maintenance of TMF and eTMF Quality Control * Database QC checks performance and documentation * Shared responsibility for preparation and attendance at internal and client/third-party audits/inspections of Data Management * Shared responsibility for follow-up on and resolution of audit findings pertaining to Data Management Training * Training of Assistant Data Managers * Project-specific training of investigators and clinical team in CRF completion Corporate/Departmental Assignments * Investigator Meetings preparation/attendance * Meetings and teleconferences organized by client/vendor preparation/attendance ## Qualifications * College or University degree or equivalent combination of training and experience that presents the required knowledge, skills and abilities * At least 3 years of experience of full scope of data management responsibilities in global EDC studies * At least 2 years of experience using CDM/EDC systems (Medidata Rave or Oracle Inform preferable) * Project data management experience is a plus * Organizational and managerial skills ## Additional Information Advance your career in clinical research and develop new skillsets whilst growing with the organization.", "summaryDescription" : "Lead Data Manager for Clinical Trials at PSI CRO. Skills: Data management, Clinical trials. Coordinate data management activities. Develop EDC", "postedDate" : "2026-06-12T20:24:53.000", "createdAt" : "2026-06-16T00:30:16.705", "lastUpdated" : "2026-06-16T12:27:18.148", "ingestTimestamp" : "2026-06-16T00:30:16.705", "mongoId" : "6a305e6cf292fd229cf70716", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Data validation", "Data entry", "Database edits", "Medical data coding", "Data management", "Clinical trials", "Clinical data management", "Project management", "Project data management", "EDC systems", "Medidata Rave", "Oracle Inform" ], "skillCount" : 12, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Lead", "dataQualityScore" : 1.0, "_score" : 715.9966, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2d3f1074d8ee00a0b347f1", "title" : "Lead Data Manager for Clinical Trials", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 125000.0, "max" : 175000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Data Manager in the Biotech industry in Mississauga, Canada, adjusted for seniority and company size." }, "location" : "Mississauga, ON, Canada", "locations" : [ "Mississauga", "ON", "Canada" ], "timestamp" : "2026-06-15T12:23:48.882", "fingerprint" : "dc6a6b6b7033d5dbc9ce9c6abfcc0bf114b7fb0580af099de03a862979b37eab", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000131984439-lead-data-manager-for-clinical-trials", "externalId" : "744000131984439", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Mississauga", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.5884727,-79.6436580" } ], "locationText" : "Mississauga, Ontario, Canada", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "technicalSkills" : "SQL, Python, R, Scala, Spark, Dbt, Snowflake, BigQuery, Redshift, Databricks, Fivetran, Airflow, Dbt Cloud, Delta Lake, Scikit-learn, TensorFlow, PyTorch, XGBoost, LightGBM, Hugging Face, MLflow, AWS, GCP, Azure", "professionalSkills" : [ "Data management", "Clinical data management", "Data collection", "Data cleaning", "Data validation", "Database management", "Quality control", "Training", "Document management" ], "hardSkillsList" : [ "Data entry", "Data inspection", "Data reconciliation", "Database edits", "CRF review", "Medical data coding", "SAE reconciliation", "Electronic data transfer" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Data entry", "level" : "intermediate" }, { "name" : "Data inspection", "level" : "intermediate" }, { "name" : "Data reconciliation", "level" : "intermediate" }, { "name" : "Database edits", "level" : "intermediate" }, { "name" : "CRF review", "level" : "intermediate" }, { "name" : "Medical data coding", "level" : "intermediate" }, { "name" : "SAE reconciliation", "level" : "intermediate" }, { "name" : "Electronic data transfer", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Data management, Clinical trials, EDC systems", "majorSkillsList" : [ "Data management", "Clinical trials", "EDC systems" ], "coreResponsibilities" : "Manage data management activities, Serve as communication point, Coordinate data management activities, Develop study documents, Develop data management plans, Review project guidelines, Perform user acceptance testing, Develop data validation plans, Develop edit check specifications, Coordinate data entry, Supervise data entry, Provide feedback on data entry, Perform data validation, Inspect data, Review data discrepancies, Resolve data discrepancies, Generate queries, Resolve queries, Provide feedback on data quality, Handle non-CRF electronic data, Archive electronic data, Load electronic data, Review reconciliation issues, Provide feedback to vendors, Perform database edits, Review manual CRFs, Perform clinical database lock, Coordinate CRF processing, Dispatch CRFs, Archive CRFs, Review CRF design, Develop CRF guidelines, Code medical data, Review coding listings, Perform SAE reconciliation, Review data transfer specifications, Approve data transfer specifications, Liaise with Document Center, Maintain TMF, Maintain eTMF, Perform database QC checks, Document QC checks, Prepare for audits, Attend audits, Attend inspections, Resolve audit findings, Train Assistant Data Managers, Provide project-specific training, Prepare investigator meetings, Attend investigator meetings, Prepare client meetings, Attend client meetings, Prepare vendor meetings, Attend vendor meetings", "teamCollaboration" : "Project teams; Company departments; Clients; Vendors; Clinical teams", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Clinical trials; EDC systems; CRF completion; Medical data coding; TMF; eTMF", "domainList" : [ "clinical-trials", "edc-systems", "crf-completion", "medical-data-coding", "tmf", "etmf" ], "domainSpecificKnowledge" : [ "Clinical trials", "EDC systems", "CRF completion", "Medical data coding", "TMF", "eTMF" ], "toolProficiency" : [ "Medidata Rave", "Oracle Inform" ], "communicationSkills" : "Client communication; Vendor communication; Project communication", "documentationSkills" : "Study documents review; Data Management plan development; Project-specific guidelines development; CRF completion guidelines development", "problemSolvingSkills" : "Data validation; Data cleaning; Data reconciliation", "qualificationsBasic" : "College or University degree, 3 years of experience, 2 years of experience using CDM/EDC systems", "qualificationsPreferred" : "Project data management experience is a plus, Medidata Rave or Oracle Inform preferable", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "We’re over 3,200+ strong across the globe. We’re scientists, strategists, creatives, and innovators. We value individual brilliance and build a strong foundation for teamwork across all our business. We love the challenge of our industry. We’re changing lives and redefining success every step of the way. The Lead Data Manager will be responsible for all data management activities in large, complex studies under general supervision, or working under minimal supervision on data management activities for small to medium sized projects. Communication * Primary communication point for project teams and company departments with regard to clinical data management * Communication line for clients/vendors for all data management aspects of clinical projects and clinical data management reporting Data Management * Coordination of data management activities within clinical projects related to EDC development, data collection, cleaning, reconciliation, Database Lock, development of final integrated database and generation of final Data Management deliverables. * Primary responsibility for clinical data management activities within clinical projects, including, but not limited to: * Study documents review * Data Management plan and other project-specific guidelines and instructions development and review * Co-ordinate/perform user acceptance testing * Development of Data Validation Plan/Edit Check Specifications * Data entry coordination and supervision, feedback to data entry personnel regarding quality of data entry and other data entry issues * Data validation, including automatic and manual data inspections, data discrepancies/deficiencies review and resolution, query generation and resolution, feedback to clinical trial teams regarding quality of data * Non-CRF electronic data handling (receiving, archiving, loading into study database, review and resolution of reconciliation issues, feedback to vendors regarding quality of data and other issues) * Database edits (paper CRF studies) * Manual CRF review (non-medical checks) * Clinical database lock * Coordination and supervision of processing, dispatch and archiving of CRFs/queries * Input into design of CRFs and other data collection forms; review Case Report Form design for accuracy and adherence to protocol * Development of CRF completion guidelines * Coding medical data with coding dictionaries and coding listings review (Lead DMs with medical/biology background, additional training required) * SAE reconciliation * Electronic data transfer (import/export) specifications review and approval Document Management * Liaison with Document Center with regard to maintenance of TMF and eTMF Quality Control * Database QC checks performance and documentation * Shared responsibility for preparation and attendance at internal and client/third-party audits/inspections of Data Management * Shared responsibility for follow-up on and resolution of audit findings pertaining to Data Management Training * Training of Assistant Data Managers * Project-specific training of investigators and clinical team in CRF completion Corporate/Departmental Assignments * Investigator Meetings preparation/attendance * Meetings and teleconferences organized by client/vendor preparation/attendance ## Qualifications * College or University degree or equivalent combination of training and experience that presents the required knowledge, skills and abilities * At least 3 years of experience of full scope of data management responsibilities in global EDC studies * At least 2 years of experience using CDM/EDC systems (Medidata Rave or Oracle Inform preferable) * Project data management experience is a plus * Organizational and managerial skills ## Additional Information Advance your career in clinical research and develop new skillsets whilst growing with the organization.", "summaryDescription" : "Lead Data Manager for Clinical Trials at PSI CRO. Skills: Data management, Clinical trials, EDC systems. Manage data management activities. Serve as communication point", "postedDate" : "2026-06-12T20:24:53.000", "createdAt" : "2026-06-14T07:43:41.389", "lastUpdated" : "2026-06-15T12:23:48.882", "ingestTimestamp" : "2026-06-14T07:43:41.389", "mongoId" : "6a2d3f1074d8ee00a0b347f1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Data entry", "Data inspection", "Data reconciliation", "Database edits", "CRF review", "Medical data coding", "SAE reconciliation", "Electronic data transfer", "Leadership", "Data management", "Clinical trials", "EDC systems", "Clinical data management", "Data collection", "Data cleaning", "Data validation", "Database management", "Quality control", "Training", "Document management", "Project management", "CRF completion", "TMF", "eTMF", "Medidata Rave", "Oracle Inform" ], "skillCount" : 26, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Lead", "dataQualityScore" : 1.0, "_score" : 714.40466, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305118f292fd229cef970e", "title" : "Clinical Operations Development Lead", "industry" : "Project Management", "salary" : { "min" : 212000.0, "max" : 291500.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "US", "locations" : [ "US" ], "timestamp" : "2026-06-16T11:38:47.399", "fingerprint" : "3ff3aeb908b710d50750a956c5b34addb534b6df35b2a4a8ffee61060109499e", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/a727b9e2-0255-4d1e-80ad-b6d2b1aa6389/apply", "externalId" : "a727b9e2-0255-4d1e-80ad-b6d2b1aa6389", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 10, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "professionalSkills" : [ "Clinical documentation", "Program management" ], "hardSkillsList" : [ "Clinical trial design", "Clinical trial execution", "Clinical trial management", "Vendor oversight", "Risk mitigation", "Budget management", "Timeline management", "Resource planning" ], "hardSkills" : [ { "name" : "Clinical trial design", "level" : "intermediate" }, { "name" : "Clinical trial execution", "level" : "intermediate" }, { "name" : "Clinical trial management", "level" : "intermediate" }, { "name" : "Vendor oversight", "level" : "intermediate" }, { "name" : "Risk mitigation", "level" : "intermediate" }, { "name" : "Budget management", "level" : "intermediate" }, { "name" : "Timeline management", "level" : "intermediate" }, { "name" : "Resource planning", "level" : "intermediate" } ], "majorSkills" : "Clinical operations, Clinical development, Global trial leadership", "majorSkillsList" : [ "Clinical operations", "Clinical development", "Global trial leadership" ], "coreResponsibilities" : "Co-lead Clinical Development Teams, Define clinical development strategies, Develop clinical development strategies, Maintain clinical development strategies, Oversee clinical trial planning, Oversee clinical trial execution, Drive creation of CDP, Maintain CDP, Lead cross-functional coordination, Identify program risks, Assess program risks, Mitigate program risks, Oversee vendor selection, Oversee CRO selection, Manage vendors, Manage CROs, Ensure inspection readiness, Ensure compliance, Provide oversight of trial design, Provide oversight of feasibility, Provide oversight of country selection, Provide oversight of site selection, Provide oversight of protocol development, Contribute to governance meetings, Contribute to program dashboards, Contribute to executive reporting, Provide line management, Support continuous improvement initiatives, Promote best practices", "teamCollaboration" : "Cross-functional coordination; Global stakeholders; Senior stakeholders", "projectManagementSkills" : [ "Project management", "Risk frameworks", "Budget management", "Timeline management", "Resource planning" ], "domainKnowledge" : "Pharmaceutical industry; Biotechnology industry; ICH-GCP guidelines; Global regulatory requirements; Rare disease development; Autoimmune development", "domainList" : [ "pharmaceutical-industry", "biotechnology-industry", "ich-gcp-guidelines", "global-regulatory-requirements", "rare-disease-development", "autoimmune-development" ], "domainSpecificKnowledge" : [ "Pharmaceutical industry", "Biotechnology industry", "ICH-GCP guidelines", "Global regulatory requirements", "Rare disease development", "Autoimmune development" ], "communicationSkills" : "Executive reporting; Influence stakeholders", "documentationSkills" : "Protocol development", "innovationCreativity" : "Innovative programs", "problemSolvingSkills" : "Risk mitigation; Issue resolution; Organizational skills; Analytical skills", "specialRequirements" : "Periodic travel", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Co-lead Clinical Development Teams (CDTs) with Medical Development Leads, ensuring alignment on clinical development strategy and execution of the Clinical Development Plan (CDP). Define, develop, and maintain clinical development strategies across indications, ensuring consistency with the Target Product Profile and overall asset strategy. Oversee end-to-end clinical trial planning and execution, including timelines, budgets, resources, and risk mitigation in collaboration with project management and finance teams. Drive creation and maintenance of the CDP, ensuring endorsement by governance bodies and alignment with strategic objectives and operational feasibility. Lead cross-functional coordination across clinical operations, medical, regulatory, biostatistics, and other stakeholders to ensure integrated execution of clinical programs. Identify, assess, and mitigate program risks, ensuring escalation when needed and driving resolution of complex operational or strategic issues. Oversee vendor and CRO selection and management, ensuring operational quality, compliance, and delivery against expectations. Ensure inspection readiness and compliance with ICH-GCP, SOPs, and applicable global regulatory requirements across all clinical activities. Provide oversight of clinical trial design, feasibility, country/site selection, and protocol development in collaboration with global stakeholders. Contribute to governance meetings, program dashboards, and executive reporting on progress, risks, and financial performance. May provide line management for Clinical Trial Managers and Clinical Trial Associates, including hiring, onboarding, performance management, and development. Support continuous improvement initiatives and promote best practices across clinical operations and development functions. Requirements: Bachelor’s or advanced degree in life sciences, medicine, pharmacy, biomedical sciences, or related field; PhD is a plus. 10+ years of experience in clinical development and/or clinical operations within the pharmaceutical or biotechnology industry, including global trial leadership responsibilities. Strong expertise in clinical trial design, execution, and management across multiple phases, including outsourced models and CRO oversight. Demonstrated experience in developing and executing clinical development strategies and integrated development plans. Strong understanding of ICH-GCP guidelines, global regulatory requirements, and clinical development best practices. Proven ability to manage complex clinical programs, including budgets, timelines, resources, and risk frameworks. Strong leadership, stakeholder management, and cross-functional collaboration skills in a global matrix environment. Excellent communication skills, with the ability to influence, align, and engage senior stakeholders across functions. Strong organizational and analytical skills with the ability to manage competing priorities and complex programs. Experience in rare disease or autoimmune clinical development is a plus. Willingness to operate in a global environment with periodic travel as required. Benefits: Competitive base salary range of $212,000 – $291,500, plus eligibility for short-term and long-term incentive programs. Comprehensive health, dental, vision, life, and disability insurance coverage. Retirement savings plan with employer matching contributions. Generous paid time off and additional well-being support programs. Performance-based incentive opportunities aligned with individual and company success. Exposure to global clinical development strategy across multiple indications and therapeutic areas. High-impact leadership role with visibility at senior governance and executive levels. Opportunity to shape innovative clinical development programs in a fast-growing biotech environment. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Clinical Operations Development Lead. Skills: Clinical operations, Clinical development, Global trial leadership. Co-lead Clinical Development Teams. Define clinical development strategies", "postedDate" : "2026-06-15T10:19:39.709", "createdAt" : "2026-06-15T10:19:39.709", "lastUpdated" : "2026-06-16T11:38:47.399", "ingestTimestamp" : "2026-06-16T03:20:48.017", "mongoId" : "6a305118f292fd229cef970e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 212000, "salaryAnnualMax" : 291500, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Clinical trial design", "Clinical trial execution", "Clinical trial management", "Vendor oversight", "Risk mitigation", "Budget management", "Timeline management", "Resource planning", "Clinical operations", "Clinical development", "Global trial leadership", "Clinical documentation", "Program management", "Project management", "Risk frameworks", "Pharmaceutical industry", "Biotechnology industry", "ICH-GCP guidelines", "Global regulatory requirements", "Rare disease development", "Autoimmune development" ], "skillCount" : 21, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 710.21655, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3084c6f292fd229c07583d", "title" : "Clinical Study Coordinator", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Clinical Study Coordinator in Chicago, adjusted for mid-seniority and full-time employment in the healthcare industry." }, "location" : "South Cook/Will County, Chicago, Illinois, United States", "locations" : [ "South Cook/Will County, Chicago", "Illinois", "United States" ], "certifications" : [ "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization" ], "timestamp" : "2026-06-16T12:57:39.777", "fingerprint" : "f1d00d59c90e88f2ed6c6e95bc5872a78e081a782c7449b87cd5b54d48ad6463", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000132293919-clinical-study-coordinator-", "externalId" : "744000132293919", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chicago", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.8755616,-87.6244212" } ], "locationText" : "Chicago, Illinois, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Study conduct tasks", "Data entry", "Monitoring visits", "Mentoring staff", "Administrative tasks", "Patient recruitment", "Patient identification", "Informed consent", "Laboratory testing", "Investigational products", "Clinical supplies", "Temperature monitoring", "Contract negotiations", "Budget negotiations", "Investigator payments", "Staff training", "Study documents", "Regulatory documents", "Regulatory correspondence", "Site improvements" ], "hardSkillsList" : [ "Protocol adherence", "Data query resolution", "Adverse event reporting", "Protocol deviation reporting", "Investigational product handling", "Site SOP adherence", "Study-specific manual adherence", "Regulatory agency inspections" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Protocol adherence", "level" : "intermediate" }, { "name" : "Data query resolution", "level" : "intermediate" }, { "name" : "Adverse event reporting", "level" : "intermediate" }, { "name" : "Protocol deviation reporting", "level" : "intermediate" }, { "name" : "Investigational product handling", "level" : "intermediate" }, { "name" : "Site SOP adherence", "level" : "intermediate" }, { "name" : "Study-specific manual adherence", "level" : "intermediate" }, { "name" : "Regulatory agency inspections", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Clinical trial coordination, Site support, Regulatory compliance", "majorSkillsList" : [ "Clinical trial coordination", "Site support", "Regulatory compliance" ], "coreResponsibilities" : "Act as communication line, Facilitate study evaluation, Provide feasibility responses, Participate in patient recruitment, Confirm eligibility, Assist with plan development, Assist in obtaining informed consent, Assist with obtaining assessments, Notify investigator of critical values, Assist with laboratory testing, Assist with processing and shipping, Assist in scheduling sponsor visits, Assist in scheduling CRO visits, Track patient recruitment, Track patient enrollment, Support enrollment targets, Provide regular updates, Ensure accurate data entry, Resolve data queries, Assist in reporting adverse events, Assist in reporting protocol deviations, Support handling investigational products, Support accountability of investigational products, Support reconciliation of investigational products, Maintain study blinding, Follow protocol guidance, Follow sponsor guidance, Follow CRO guidance, Assist site staff with temperature monitoring, Support contract negotiations, Support budget negotiations, Oversee Investigator payments, Oversee Site Payments, Ensure staff training completion, Complete retraining for protocol changes, Ensure investigator reviews documents, Ensure investigator signs documents, Provide guidance on requirements, Educate research team, Maintain study documents, Prepare for study visits, Prepare for audits, Prepare for inspections, Prepare regulatory documents, Submit regulatory documents, Submit correspondence to regulatory authorities, Submit correspondence to IRBs, Involve in on-site training, Assist with identifying areas for improvement, Develop tools for improvements, Maintain licensure, Maintain certifications, Perform assigned tasks, Consult manager for out-of-scope tasks", "teamCollaboration" : "Milestone One; Sponsor representatives; CRO representatives; Medical institution; Ancillary departments; Local research team; Site staff", "domainKnowledge" : "Clinical trial conduct; Human subjects research; Local laws; Federal laws; Study protocols; Site SOPs; Study-specific lab manuals; Investigational products; Clinical supplies; Regulatory authorities; Institutional review boards", "domainList" : [ "clinical-trial-conduct", "human-subjects-research", "local-laws", "federal-laws", "study-protocols", "site-sops", "study-specific-lab-manuals", "investigational-products", "clinical-supplies", "regulatory-authorities", "institutional-review-boards" ], "domainSpecificKnowledge" : [ "Clinical trial conduct", "Human subjects research", "Local laws", "Federal laws", "Study protocols", "Site SOPs", "Study-specific lab manuals", "Investigational products", "Clinical supplies", "Regulatory authorities", "Institutional review boards" ], "toolProficiency" : [ "EDC systems" ], "documentationSkills" : "Source documentation; Study documents; Regulatory documents", "problemSolvingSkills" : "Resolve study specific issues; Resolve data queries", "outcomesObjectives" : "Ensure responses provided in due time; Ensure enrollment targets are met; Ensure accurate and timely data entry; Ensure staff training completion; Ensure investigator reviews and signs documents", "qualificationsBasic" : "2 years experience coordinating clinical research studies, Current Good Clinical Practice (GCP), International Air Transport Association (IATA), Current Basic Cardiopulmonary Resuscitation (CPR), Phlebotomy certification unless part of active professional licensure (RN or LPN)", "qualificationsPreferred" : "Nephrology experience, Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. Tasks may include activities associated with the assessment of the feasibility of new/potential clinical studies, conducting research-related visits as outlined in the respective protocol, assisting the site with logistics of scheduling research visits and testing per the schedule of events in the protocol, collaboration with ancillary departments involved in the research visit to assist in a smooth patient flow at research visits., general study conduct tasks, assistance with data entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In addition, mentoring staff and administrative tasks as assigned by the Milestone One Manager. In this job you will: * Acts as a constant line of communication between Milestone One, the Sponsor or CRO, and the medical institution. * Facilitates the evaluation of proposed studies and ensures responses to feasibility questions are provided in due time. * Actively participates in patient recruitment/identification and evaluation for study inclusion by confirming eligibility according to the Inclusion and exclusion criteria. * Assists with plan development for new recruitment / retention tools, source documentation and other site tools to enhance quality and time management of research staff. * Assists the local research team in obtaining informed consent before study entry or any study-related procedures or tests being performed. * Assist with obtaining the required assessments at each visit per the protocol and notify the investigator of any critical values that need immediate attention or would prohibit or delay study treatment. * Assist with obtaining local and central laboratory testing, processing, and shipping per site SOP and study-specific lab manual. * Assist in scheduling and preparation for all types of sponsors or CRO representative visits at the medical institution. * Track patient recruitment and enrollment and actively supports the medical site team to ensure enrollment targets are met at the site level. Provides regular updates to the staff and investigators regarding study amendments. * Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to guidelines and investigator instructions. * Support proper handling, accountability, and reconciliation of all investigational products and clinical supplies. If applicable, always maintain the study blinding. Protocol and sponsor/CRO guidance will be followed if a study participant requires unblinding. * Assist site staff with maintaining appropriate temperature monitoring for study products and supplies. * Support the contract and budget negotiations and oversees Investigator/Site Payments. * Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial. Retraining will be completed for changes to the protocol before site implementation. * Be responsible for ensuring the investigator reviews and signs study documents appropriately and within a reasonable period. Guidance should be provided to educate the site research team on requirements for conducting clinical trials, date format, etc. * Actively participate in maintaining study documents at the medical institution in preparation for on-site study visits/audits or regulatory agency inspections. * Assist with preparing and submitting regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs). * May be involved in the on-site training of additional staff as part of the SEO or other education programs. * Assist with identifying areas that need improvement for specific sites and assists with developing tools to assist with improvements. * Maintain all licensure and certifications applicable to the role of SEO site/Study coordinator II. * SEO SC is responsible for only performing assigned tasks within their training and licensure if applicable. SEO SC should immediately consult the assigned Milestone One manager for tasks that do not fall within their scope. ## Qualifications Education Relevant education and at least two years of experience coordinating clinical research studies involving human subjects OR, if allowed by local regulations, on-the-job training with at least two years of experience coordinating clinical research studies involving human subjects. Nephrology experience preferred. Certifications * Current Good Clinical Practice (GCP) * International Air Transport Association (IATA) * Current Basic Cardiopulmonary Resuscitation (CPR) * Phlebotomy certification unless part of active professional licensure (RN or LPN) * Preferred Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization. May be obtained within (1) year of employment or status change if not currently certified. ## Additional Information Located in South Cook/ Will County, Chicago (On-site position). If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you!", "summaryDescription" : "Clinical Study Coordinator at PSI CRO. Skills: Clinical trial coordination, Site support, Regulatory compliance. Act as communication line. Facilitate study evaluation", "postedDate" : "2026-06-15T22:35:56.000", "createdAt" : "2026-06-16T01:41:10.308", "lastUpdated" : "2026-06-16T12:57:39.777", "ingestTimestamp" : "2026-06-16T01:41:10.308", "mongoId" : "6a3084c6f292fd229c07583d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Protocol adherence", "Data query resolution", "Adverse event reporting", "Protocol deviation reporting", "Investigational product handling", "Site SOP adherence", "Study-specific manual adherence", "Regulatory agency inspections", "Leadership", "Clinical trial coordination", "Site support", "Regulatory compliance", "Study conduct tasks", "Data entry", "Monitoring visits", "Mentoring staff", "Administrative tasks", "Patient recruitment", "Patient identification", "Informed consent", "Laboratory testing", "Investigational products", "Clinical supplies", "Temperature monitoring", "Contract negotiations", "Budget negotiations", "Investigator payments", "Staff training", "Study documents", "Regulatory documents", "Regulatory correspondence", "Site improvements", "Clinical trial conduct", "Human subjects research", "Local laws", "Federal laws", "Study protocols", "Site SOPs", "Study-specific lab manuals", "Regulatory authorities", "Institutional review boards", "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "EDC systems" ], "skillCount" : 47, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "_score" : 707.3709, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2cb20e74d8ee00a09df75c", "title" : "Principal, Global Feasibility (pre-award strategy)", "industry" : "Analyst", "salary" : { "min" : 115000.0, "max" : 165000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Principal in Biotech in the Netherlands, adjusted for seniority and industry." }, "location" : "Netherlands", "locations" : [ "Netherlands" ], "timestamp" : "2026-06-16T06:10:11.989", "fingerprint" : "6c03434fe1c071cf613d14fb3624044e105e5a66bb855075a6bdc60506210292", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/6f23e5d3-d623-420a-99ba-481e9d5c9063/apply", "externalId" : "6f23e5d3-d623-420a-99ba-481e9d5c9063", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Netherlands", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "Netherlands", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Global feasibility", "Pre-award strategy", "Clinical trial design", "Site selection", "Feasibility strategy", "Data-driven insights", "Feasibility solutions", "Operational soundness", "Strategic alignment", "Assignment management", "Process improvement", "Best practices development", "Feasibility assessments", "Partnership feasibility", "Site-level feasibility", "Feasibility strategies", "Feasibility requests", "Evidence-based decisions", "Bid defense preparation", "Data management", "Feasibility frameworks", "Feasibility methodologies" ], "hardSkillsList" : [ "Scientific literature research", "External source research", "Analysis", "Reporting" ], "softSkillsList" : [ "Autonomy" ], "hardSkills" : [ { "name" : "Scientific literature research", "level" : "intermediate" }, { "name" : "External source research", "level" : "intermediate" }, { "name" : "Analysis", "level" : "intermediate" }, { "name" : "Reporting", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Autonomy" } ], "majorSkills" : "Global feasibility, Pre-award strategy, Clinical research, Feasibility strategy", "majorSkillsList" : [ "Global feasibility", "Pre-award strategy", "Clinical research", "Feasibility strategy" ], "coreResponsibilities" : "Lead and independently deliver highly complex global feasibility, Develop feasibility strategies across all therapeutic areas, Develop feasibility work for RFP and partnership feasibility, Analyze site-level feasibility outputs, Present site-level feasibility outputs, Collaborate cross-functionally with business development, Collaborate with medical directors, Collaborate with business analysts, Collaborate with operational teams, Design optimal feasibility strategies, Identify innovative solutions for non-standard feasibility requests, Propose innovative solutions for complex feasibility requests, Conduct advanced research using scientific literature, Conduct advanced research using internal data systems, Conduct advanced research using external sources, Support bid defense preparation, Participate in client-facing meetings, Maintain accurate documentation, Ensure high-quality data management within internal systems, Ensure high-quality data management within knowledge repositories, Contribute to the development of departmental metrics, Contribute to the development of feasibility frameworks, Contribute to the development of process improvements, Mentor junior team members, Support junior team members, Provide guidance on analysis, Provide guidance on reporting, Provide guidance on best practices, Mentor mid-level team members, Support mid-level team members, Participate in strategic initiatives, Participate in system development, Participate in data asset evaluation, Participate in continuous improvement of feasibility methodologies", "teamCollaboration" : "Cross-functional teams; Global teams; Business development teams; Medical teams; Analytics teams; Operations teams", "domainKnowledge" : "Global clinical feasibility; Country and site selection; Drug development lifecycle; Therapeutic areas; Clinical trial design; Life Sciences; Clinical research; GCP; Study start-up; RFP requirements", "domainList" : [ "global-clinical-feasibility", "country-and-site-selection", "drug-development-lifecycle", "therapeutic-areas", "clinical-trial-design", "life-sciences", "clinical-research", "gcp", "study-start-up", "rfp-requirements" ], "domainSpecificKnowledge" : [ "Global clinical feasibility", "Country and site selection", "Drug development lifecycle", "Therapeutic areas", "Clinical trial design", "Life Sciences", "Clinical research", "GCP", "Study start-up", "RFP requirements" ], "communicationSkills" : "Written communication; Verbal communication; Presentation abilities; Senior stakeholder engagement", "documentationSkills" : "Accurate documentation", "continuousLearning" : "Continuous learning opportunities; Training; Professional development support", "innovationCreativity" : "Innovative solutions", "problemSolvingSkills" : "Problem-solving skills; Synthesize complex data sets", "outcomesObjectives" : "Shape high-quality feasibility strategies; Influence clinical trial design; Influence site selection; Influence study success; Translate complex RFP requirements into actionable, data-driven insights; Ensure feasibility solutions are operationally sound; Ensure feasibility solutions are strategically aligned; Manage multiple high-complexity assignments simultaneously; Enhance operational efficiency", "qualificationsBasic" : "Advanced degree in Life Sciences or related field (BS/RN/MS with 7+ years of experience, or PhD/MD with 3+ years of relevant experience), Background in clinical research, Clinical trial execution experience, GCP understanding, Study start-up processes experience, Deep knowledge of global clinical feasibility, Country and site selection knowledge, Drug development lifecycle knowledge, Proven ability to independently manage complex, multi-study workloads under tight deadlines, High attention to detail, Analytical skills, Strategic thinking skills, Problem-solving skills, Ability to synthesize complex data sets into clear insights, Excellent communication skills, Written communication abilities, Verbal communication abilities, Presentation abilities for senior stakeholder engagement, Demonstrated ability to influence, Demonstrated ability to negotiate, Ability to work effectively in cross-functional, global teams, Experience in customer-facing or consultancy-style roles within clinical research or life sciences environments, Ability to mentor and support junior colleagues, Organizational skills, Ability to manage competing priorities in a fast-paced environment", "qualificationsPreferred" : "Experience with Python and machine learning frameworks, Kubernetes experience a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "## Description This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Principal, Global Feasibility (pre-award strategy) based in Netherlands. In this senior-level role, you will act as a key strategic expert in global clinical feasibility, supporting complex pre-award activities across a wide range of therapeutic areas. You will be responsible for shaping high-quality feasibility strategies that directly influence clinical trial design, site selection, and study success. Working in a fast-paced, global environment, you will collaborate closely with business development, medical, analytics, and operations teams to translate complex RFP requirements into actionable, data-driven insights. This role requires strong scientific understanding combined with commercial awareness, ensuring feasibility solutions are both operationally sound and strategically aligned. You will operate with a high degree of autonomy, managing multiple high-complexity assignments simultaneously across global studies. Acting as a senior representative of feasibility, you will also contribute to mentoring, process improvement, and the development of best practices. This is a highly impactful position for an experienced clinical research professional seeking to shape global study success at scale. ## Accountabilities Lead and independently deliver highly complex global feasibility and pre-award strategy assessments across all therapeutic areas, including RFP and partnership feasibility work. Develop, analyze, and present site-level feasibility outputs in both written and presentation formats for internal and external stakeholders. Collaborate cross-functionally with business development, medical directors, business analysts, and operational teams to design optimal feasibility strategies. Identify and propose innovative solutions for non-standard or complex feasibility requests with minimal supervision. Conduct advanced research using scientific literature, internal data systems, and external sources to support evidence-based feasibility decisions. Support bid defense preparation and participate in client-facing meetings with a high level of professionalism and autonomy. Maintain accurate documentation and ensure high-quality data management within internal systems and knowledge repositories. Contribute to the development of departmental metrics, feasibility frameworks, and process improvements to enhance operational efficiency. Mentor and support junior and mid-level team members, providing guidance on analysis, reporting, and best practices. Participate in strategic initiatives, including system development, data asset evaluation, and continuous improvement of feasibility methodologies. Requirements Advanced degree in Life Sciences or related field (BS/RN/MS with 7+ years of experience, or PhD/MD with 3+ years of relevant experience). Strong background in clinical research, including clinical trial execution, GCP understanding, and study start-up processes. Deep knowledge of global clinical feasibility, country and site selection, and drug development lifecycle. Proven ability to independently manage complex, multi-study workloads under tight deadlines while maintaining high attention to detail. Strong analytical, strategic thinking, and problem-solving skills with the ability to synthesize complex data sets into clear insights. Excellent communication skills, including written, verbal, and presentation abilities for senior stakeholder engagement. Demonstrated ability to influence, negotiate, and work effectively in cross-functional, global teams. Experience in customer-facing or consultancy-style roles within clinical research or life sciences environments. Ability to mentor and support junior colleagues while contributing to team capability development. Strong organizational skills with the ability to manage competing priorities in a fast-paced environment. Benefits Competitive compensation and comprehensive global benefits package. Opportunity to work on high-impact, global clinical research programs across multiple therapeutic areas. Strong career development and advancement opportunities within a leading life sciences environment. Exposure to cutting-edge clinical development strategies and global feasibility operations. Collaborative, international, and science-driven work culture. Flexible working arrangements supporting work-life balance. Continuous learning opportunities, including training and professional development support. Participation in high-visibility projects influencing global drug development success. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Principal, Global Feasibility (pre-award strategy). Skills: Global feasibility, Pre-award strategy, Clinical research, Feasibility strategy. Lead and independently deliver highly complex global feasibility. Develop feasibility strategies across all therapeutic areas", "postedDate" : "2026-06-12T12:28:18.241", "createdAt" : "2026-06-12T12:28:18.241", "lastUpdated" : "2026-06-16T06:10:11.989", "ingestTimestamp" : "2026-06-14T21:32:53.430", "mongoId" : "6a2cb20e74d8ee00a09df75c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Scientific literature research", "External source research", "Analysis", "Reporting", "Autonomy", "Global feasibility", "Pre-award strategy", "Clinical research", "Feasibility strategy", "Clinical trial design", "Site selection", "Data-driven insights", "Feasibility solutions", "Operational soundness", "Strategic alignment", "Assignment management", "Process improvement", "Best practices development", "Feasibility assessments", "Partnership feasibility", "Site-level feasibility", "Feasibility strategies", "Feasibility requests", "Evidence-based decisions", "Bid defense preparation", "Data management", "Feasibility frameworks", "Feasibility methodologies", "Global clinical feasibility", "Country and site selection", "Drug development lifecycle", "Therapeutic areas", "Life Sciences", "GCP", "Study start-up", "RFP requirements" ], "skillCount" : 36, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "_score" : 700.29645, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 } ], "status" : 200, "message" : "OK", "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 118585, "totalPages" : 2372, "hasNext" : true, "hasPrevious" : false } }

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