{ "count" : 16282, "data" : [ { "id" : "6a2b11bf74d8ee00a0767441", "title" : "External Research and Collaborations Director", "company" : "Oxford Quantum Circuits", "industry" : "Computer Hardware", "salary" : { "min" : 120000.0, "max" : 180000.0, "currency" : "GBP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director in the Technology industry in Reading, UK, adjusted for seniority and company size." }, "location" : "Reading, England, United Kingdom", "locations" : [ "Reading, England, United Kingdom" ], "timestamp" : "2026-06-15T00:37:08.496", "fingerprint" : "59dcfaf00bab25c398a27f99c9e232f849ae861a5a7a085063c44d609385ee0b", "source" : "workable", "language" : "en", "applyUrl" : "https://apply.workable.com/j/825FDD22A7/apply", "externalId" : "825FDD22A7", "industryFunction" : { }, "locationPoint" : "51.45625,-0.97113", "structuredLocations" : [ { "city" : "Reading", "state" : "England", "country" : "United Kingdom", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "51.4564242,-0.9700664" } ], "locationText" : "Reading, England, United Kingdom", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "professionalSkills" : [ "Strategic planning", "Grant development", "Programme management", "Stakeholder engagement", "Budgeting", "Forecasting", "Risk management", "Technical proposal development", "Research prioritisation", "Funding strategy", "Budget planning", "Resource allocation", "Business planning", "Strategic prioritisation", "Budget forecasting", "Resource planning", "Research commercialisation" ], "hardSkillsList" : [ "Quantum technologies", "Quantum computing", "Quantum hardware", "Physics", "Engineering", "Deep-tech", "Complex programmes", "Scientific initiatives", "Grant funding", "Technical concepts", "Scientific concepts" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Quantum technologies", "level" : "intermediate" }, { "name" : "Quantum computing", "level" : "intermediate" }, { "name" : "Quantum hardware", "level" : "intermediate" }, { "name" : "Physics", "level" : "intermediate" }, { "name" : "Engineering", "level" : "intermediate" }, { "name" : "Deep-tech", "level" : "intermediate" }, { "name" : "Complex programmes", "level" : "intermediate" }, { "name" : "Scientific initiatives", "level" : "intermediate" }, { "name" : "Grant funding", "level" : "intermediate" }, { "name" : "Technical concepts", "level" : "intermediate" }, { "name" : "Scientific concepts", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "External research collaborations, Strategic partnerships, Grant funding programmes, Quantum technology roadmap", "majorSkillsList" : [ "External research collaborations", "Strategic partnerships", "Grant funding programmes", "Quantum technology roadmap" ], "coreResponsibilities" : "Define external research strategy, Execute external research strategy, Define collaboration strategy, Execute collaboration strategy, Identify grant funding opportunities, Prioritise grant funding opportunities, Secure grant funding opportunities, Lead grant applications, Lead funded programmes, Coordinate stakeholders, Coordinate budgets, Coordinate governance, Coordinate reporting, Coordinate partner engagement, Build senior relationships, Maintain senior relationships, Create collaboration opportunities, Drive research prioritisation, Drive funding strategy, Drive budget planning, Drive resource allocation, Ensure collaboration programmes delivered, Manage risks, Manage dependencies, Manage governance requirements, Manage stakeholder expectations, Drive cross-functional alignment", "teamCollaboration" : "Cross-functional alignment; Science teams; Engineering teams; Product teams; Finance teams; Legal teams; Commercial teams; People teams", "projectManagementSkills" : [ "Programme management", "Grant funding programmes", "Complex programmes", "Milestones", "Budgets", "Governance frameworks", "Reporting requirements" ], "domainKnowledge" : "Quantum technologies; Quantum computing; Quantum hardware; Deep-tech environment; UKRI; Innovate UK; Horizon Europe; EPSRC", "domainList" : [ "quantum-technologies", "quantum-computing", "quantum-hardware", "deep-tech-environment", "ukri", "innovate-uk", "horizon-europe", "epsrc" ], "domainSpecificKnowledge" : [ "Quantum technologies", "Quantum computing", "Quantum hardware", "Deep-tech environment", "UKRI", "Innovate UK", "Horizon Europe", "EPSRC" ], "communicationSkills" : "Translate scientific concepts; Translate technical concepts; Clear proposals; Clear plans; Clear decisions; Stakeholder communications", "innovationCreativity" : "Bold innovation", "outcomesObjectives" : "Accelerate technology roadmap; Strengthen scientific influence; Unlock funding opportunities; Support business growth; Deliver technical outcomes; Deliver commercial outcomes", "qualificationsBasic" : "Significant experience leading external research collaborations, Significant experience leading strategic partnerships, Significant experience leading grant-funded programmes, Significant experience leading scientific initiatives, Background within quantum technologies, Background within quantum computing, Background within quantum hardware, Background within physics, Background within engineering, Background within deep-tech environment, Proven ability to influence senior stakeholders, Experience managing relationships with universities, Experience managing relationships with research institutions, Experience managing relationships with funding bodies, Experience managing relationships with industry partners, Experience managing relationships with comparable organisations, Demonstrated success delivering complex programmes, Experience contributing to business planning, Experience contributing to strategic prioritisation, Experience contributing to budget forecasting, Experience contributing to resource planning, Excellent ability to translate complex concepts, Degree in Physics, Degree in Engineering, Degree in Quantum Technology, Degree in Computer Science, Equivalent practical experience, Expertise in strategic planning, Expertise in grant development, Expertise in programme management, Expertise in stakeholder engagement, Expertise in budgeting, Expertise in forecasting, Expertise in risk management, Expertise in technical proposal development", "qualificationsPreferred" : "Experience securing grant funding, Experience managing grant funding, Experience within scale-up environment, Experience within commercial R&D, Experience within high-growth technology environment, Background in shaping research strategy, Exposure to intellectual property management, Exposure to collaboration agreements, Exposure to research governance, Experience leading teams, Experience leading matrix organisations, Experience leading cross-functional delivery groups, PhD in quantum physics, PhD in quantum computing, PhD in superconducting circuits, PhD in engineering, PhD in related field, MSc in quantum physics, MSc in quantum computing, MSc in superconducting circuits, MSc in engineering, MSc in related field, Equivalent research experience, Knowledge of partnership governance, Knowledge of research commercialisation, Knowledge of change leadership, Knowledge of data analysis, Knowledge of talent planning", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At OQC, we aren’t just theorising about the future; we’re building it. Born from a philosophy of bold innovation, we’ve successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we’re just getting started and we’ve recently closed our £260 million Series C funding round – the largest fundraise ever completed by a quantum computing company in Europe. As External Research and Collaborations Director, you will shape and lead OQC’s external research ecosystem, turning scientific collaboration opportunities into funded, strategically aligned programmes that accelerate our technology roadmap. Working closely with our Founder and senior leadership team, you’ll build high-impact partnerships that strengthen OQC’s scientific influence, unlock funding opportunities, and support long-term business growth. ### The Role You will own OQC’s approach to research partnerships, grant funding, and external collaborations, ensuring that scientific priorities are translated into well-governed, executable programmes that deliver meaningful technical and commercial outcomes. ### What You'll Be Working On * Defining and executing OQC’s external research and collaboration strategy across universities, research institutions, funding bodies, industry partners, and the wider quantum ecosystem. * Identifying, prioritising, and securing strategic grant funding opportunities aligned with OQC’s technical roadmap and business objectives. * Leading end-to-end delivery of grant applications and funded programmes, coordinating stakeholders, budgets, governance, reporting, and partner engagement. * Building and maintaining senior relationships with academic, research, industry, and funding organisations to create high-value collaboration opportunities. * Partnering with Science and Innovation leadership to drive research prioritisation, funding strategy, budget planning, and resource allocation. * Ensuring collaboration programmes are delivered effectively, proactively managing risks, dependencies, governance requirements, and stakeholder expectations. * Driving cross-functional alignment across Science, Engineering, Product, Finance, Legal, Commercial, and People teams to maximise collaboration success and business impact. ### What We're Looking For * Significant experience leading complex external research collaborations, strategic partnerships, grant-funded programmes, or equivalent scientific initiatives. * Strong background within quantum technologies, quantum computing, quantum hardware, physics, engineering, or another deep-tech environment. * Proven ability to influence senior scientific, technical, commercial, and operational stakeholders in complex and ambiguous environments. * Experience managing relationships with universities, research institutions, funding bodies, industry partners, or comparable organisations. * Demonstrated success delivering complex programmes against milestones, budgets, governance frameworks, and reporting requirements. * Experience contributing to business planning, strategic prioritisation, budget forecasting, and resource planning within technical or scientific organisations. * Excellent ability to translate complex scientific and technical concepts into clear proposals, plans, decisions, and stakeholder communications. * Degree in Physics, Engineering, Quantum Technology, Computer Science, or a related scientific discipline, or equivalent practical experience. * Expertise in strategic planning, grant development, programme management, stakeholder engagement, budgeting, forecasting, risk management, and technical proposal development. ### The 'Nice-to-Haves' * Experience securing or managing significant grant funding through organisations such as UKRI, Innovate UK, Horizon Europe, EPSRC, or similar funding bodies. * Experience within a scale-up, commercial R&D, or high-growth technology environment. * Background in shaping research strategy alongside academic or industry collaborators. * Exposure to intellectual property management, collaboration agreements, and research governance. * Experience leading teams, matrix organisations, or cross-functional delivery groups. * PhD, MSc, or equivalent research experience in quantum physics, quantum computing, superconducting circuits, engineering, or a related field. * Knowledge of partnership governance, research commercialisation, change leadership, data analysis, and talent planning. ### Why Join OQC You will join a world-class team at the forefront of the next computational era. We offer a culture of bold innovation, the chance to work with unique lab infrastructure, and the opportunity to see your work redefine the limits of computation. Learn more about our benefits and positive work culture here:", "summaryDescription" : "External Research and Collaborations Director at Oxford Quantum Circuits. Skills: External research collaborations, Strategic partnerships, Grant funding programmes, Quantum technology roadmap. Define external research strategy. Execute external research strategy", "postedDate" : "2026-06-11T00:00:00.000", "createdAt" : "2026-06-12T07:06:14.471", "lastUpdated" : "2026-06-15T00:37:08.496", "ingestTimestamp" : "2026-06-12T07:06:14.471", "mongoId" : "6a2b11bf74d8ee00a0767441", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://apply.workable.com/j/825FDD22A7", "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Quantum technologies", "Quantum computing", "Quantum hardware", "Physics", "Engineering", "Deep-tech", "Complex programmes", "Scientific initiatives", "Grant funding", "Technical concepts", "Scientific concepts", "Leadership", "External research collaborations", "Strategic partnerships", "Grant funding programmes", "Quantum technology roadmap", "Strategic planning", "Grant development", "Programme management", "Stakeholder engagement", "Budgeting", "Forecasting", "Risk management", "Technical proposal development", "Research prioritisation", "Funding strategy", "Budget planning", "Resource allocation", "Business planning", "Strategic prioritisation", "Budget forecasting", "Resource planning", "Research commercialisation", "Milestones", "Budgets", "Governance frameworks", "Reporting requirements", "Deep-tech environment", "UKRI", "Innovate UK", "Horizon Europe", "EPSRC" ], "skillCount" : 42, "jobCategory" : "other", "jobSubcategory" : "computer-hardware", "seniorityLevel" : "executive", "dataQualityScore" : 1.0, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Quantum Computing" }, { "id" : "6a2c6c7574d8ee00a0918d69", "title" : "Clinical Research Assistant", "company" : "Care Access", "industry" : "Healthcare", "salary" : { "min" : 42000.0, "max" : 58000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an Entry-level Clinical Research Assistant in Georgia, United States, with adjustments for the healthcare industry and company size." }, "location" : "Georgia, United States", "locations" : [ "Georgia", "United States" ], "timestamp" : "2026-06-15T08:41:04.799", "fingerprint" : "7ef9e37df56a30580bdf3a300fb43b82d861522ce4c709d76096f95f28888882", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/careaccess/jobs/4282670009", "externalId" : "4282670009", "industryFunction" : { }, "structuredLocations" : [ { "state" : "Georgia", "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "Georgia, United States", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "professionalSkills" : [ "Care coordination", "Patient care" ], "hardSkillsList" : [ "Phlebotomy", "Specimen collection", "Specimen processing", "Specimen shipping" ], "softSkillsList" : [ "Critical thinking", "Problem solver" ], "hardSkills" : [ { "name" : "Phlebotomy", "level" : "intermediate" }, { "name" : "Specimen collection", "level" : "intermediate" }, { "name" : "Specimen processing", "level" : "intermediate" }, { "name" : "Specimen shipping", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Critical thinking" }, { "name" : "Problem solver" } ], "majorSkills" : "Clinical research, Patient recruitment, Data collection", "majorSkillsList" : [ "Clinical research", "Patient recruitment", "Data collection" ], "coreResponsibilities" : "Understand and follow SOPs, Participate in recruitment events, Assist with outreach materials, Identify potential participants, Review medical records, Review study charts, Review subject database, Assist with recruitment, Conduct phone screenings, Request medical records, Schedule visits with participants, Contact with reminders, Obtain informed consent, Complete visit procedures, Collect specimens, Process specimens, Ship specimens, Record data legibly, Enter data in real time, Request study participant payments, Update internal trackers, Update online recruitment systems, Assist with query resolution, Assist with administrative tasks, Assist with maintaining site logs, Assist with inventory, Order equipment, Order supplies, Maintain adherence FDA regulations, Maintain adherence ICH guidelines, Maintain effective relationships, Interact professionally, Communicate clearly verbally, Communicate clearly in writing, Perform other duties", "teamCollaboration" : "Study participants; Care Access Research personnel; Patients; Sponsor representatives; Investigators; Management", "domainKnowledge" : "Medical terminology; Research terminology; Federal regulations; Good Clinical Practices; FDA regulations; ICH guidelines", "domainList" : [ "medical-terminology", "research-terminology", "federal-regulations", "good-clinical-practices", "fda-regulations", "ich-guidelines" ], "domainSpecificKnowledge" : [ "Medical terminology", "Research terminology", "Federal regulations", "Good Clinical Practices", "FDA regulations", "ICH guidelines" ], "toolProficiency" : [ "Microsoft Office Suite" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "E-source documents; Site logs", "problemSolvingSkills" : "Critical thinker; Problem solver", "specialRequirements" : "Regional commute requirements, Regularly planned travel, Minimal overnight travel", "qualificationsBasic" : "1-year working experience, Bilingual in Spanish, Working knowledge medical terminology, Working knowledge research terminology, Working knowledge federal regulations, Working knowledge Good Clinical Practices, Proficiency Microsoft Office Suite, Phlebotomy Experience Required, Phlebotomy Proficiency Required", "qualificationsPreferred" : "Clinical Research experience preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "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 Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This position has potential growth and advancement within the Care Access Research organization. How You'll Make An Impact Ability to understand and follow institutional SOPs Participate in recruitment and pre-screening events (may be at another location) Assist with preparation of outreach materials Identify potential participants by reviewing medical records, study charts and subject database Assist with recruitment of new participants by conducting phone screenings Request medical records of potential and current research participants Schedule visits with participants, contact with reminders Obtain informed consent per Care Access Research SOP, under the direction of the CRC Complete visit procedures as required by protocol, under the direction of the CRC Collect, process and ship specimens as directed by protocol, under the direction of the CRC Record data legibly and enter in real time on paper or e-source documents Request study participant payments Update all applicable internal trackers and online recruitment systems Assist with query resolution Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc. Assist with maintaining all site logs Assist with inventory and ordering equipment and supplies Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. Maintain effective relationships with study participants and other care Access Research personnel. Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management. Communicate clearly verbally and in writing. Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. The Expertise Required Bilingual in Spanish required Ability and willingness to work independently with minimal supervision   Ability to learn to work in a fast-paced environment   Excellent communication skills and a high degree of professionalism with all types of people Excellent organizational skills with strong attention to detail   A working knowledge of medical and research terminology   A working knowledge of federal regulations, Good Clinical Practices (GCP)   Critical thinker and problem solver   Friendly, outgoing personality with the ability to maintain a positive attitude under pressure   Contribute to team and site goals   Proficiency in Microsoft Office Suite   High level of self-motivation and energy   An optimistic, “can do” attitude   Certifications/Licenses, Education, and Experience: A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist. Phlebotomy Experience and Proficiency Required Some Clinical Research experience preferred   How We Work Together Location: This is an on-site position with regional commute requirements. Travel: Regularly planned travel within the region will be required as part of the role. Overnight travel will be minimal (<10%). Physical demands associated with this position Include: The ability to use keyboards and other computer equipment. The expected salary range for this role is $19.00 - $33.00 USD per hour for full time team members. Benefits & Perks (US Full Time Employees) Paid Time Off (PTO) and Company Paid Holidays 100% Employer paid medical, dental, and vision insurance plan options Health Savings Account and Flexible Spending Accounts Bi-weekly HSA employer contribution Company paid Short-Term Disability and Long-Term Disability 401(k) Retirement Plan, with Company Match 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 Research Assistant at Care Access. Skills: Clinical research, Patient recruitment, Data collection. Understand and follow SOPs. Participate in recruitment events", "postedDate" : "2026-06-14T05:24:38.454", "createdAt" : "2026-06-14T05:24:38.454", "lastUpdated" : "2026-06-15T08:41:04.799", "ingestTimestamp" : "2026-06-14T05:24:38.454", "mongoId" : "6a2c6c7574d8ee00a0918d69", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 42000, "salaryAnnualMax" : 58000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Phlebotomy", "Specimen collection", "Specimen processing", "Specimen shipping", "Critical thinking", "Problem solver", "Clinical research", "Patient recruitment", "Data collection", "Care coordination", "Patient care", "Medical terminology", "Research terminology", "Federal regulations", "Good Clinical Practices", "FDA regulations", "ICH guidelines", "Microsoft Office Suite" ], "skillCount" : 18, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c7ea474d8ee00a0953106", "title" : "Clinical Research Coordinator", "company" : "Headlands Research", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Research Coordinator in Chesterfield, United States, adjusted for industry and company size." }, "location" : "Chesterfield, Missouri, United States", "locations" : [ "Chesterfield", "Missouri", "United States" ], "timestamp" : "2026-06-15T21:26:14.712", "fingerprint" : "1bc7d208748eaa904ae1556fff4f3dae67bff3065e560806e3d0dd3e6554c7ad", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/headlandsresearch/jobs/4283743009", "externalId" : "4283743009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chesterfield", "state" : "Missouri", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.6581764,-90.5680617" } ], "locationText" : "Chesterfield, Missouri, United States", "employmentType" : "FULL_TIME", "remoteFriendly" : false, "rawDescription" : "At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. Clinical Research Coordinator (CRC) \uD83D\uDCCD Location: Chesterfield, MO | \uD83C\uDFE5 Site Name: Clinical Research Professionals LLC | \uD83D\uDD52 Full-Time | \uD83E\uDDEA Clinical Research Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials. We’re seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Chesterfield, MO. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry. Type: Full-time Schedule: Mondays through Fridays, 8:00am - 4:00pm Location: Onsite in Springfield, MO (no capabilities for remote or hybrid work) Reports to: Clinical Research Manager Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more. \uD83D\uDCBC What We Offer Competitive pay + annual performance incentives Medical, dental, and vision insurance 401(k) plan with company match Paid time off (PTO) and company holidays A mission-driven culture focused on advancing medicine and improving patient outcomes \uD83D\uDE80 Why Join Us? You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you. Responsibilities: Coordinate all aspects of assigned clinical trials from site initiation to study close-out Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs Manage subject recruitment, informed consent, and retention strategies Ensure timely data entry and resolution of EDC queries Report and follow up on all adverse events, serious adverse events, and deviations Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders Prepare for and participate in monitoring visits, audits, and inspections Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained) Attend investigator meetings and provide cross-functional support as needed Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control Requirements: Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP Previous experience as a Clinical Research Coordinator Industry-sponsored trial experience strongly preferred (vaccine study experience a plus) Familiarity with electronic data capture (EDC), IVRS, and other trial platforms Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures Proficiency in medical terminology and clinical documentation practices Strong interpersonal, verbal, and written communication skills Organized, detail-oriented, and capable of managing multiple priorities Proficient in Microsoft Office and other clinical research systems Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind. Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Need Assistance? Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.", "summaryDescription" : "Clinical Research Coordinator at Headlands Research", "postedDate" : "2026-06-14T19:11:02.941", "createdAt" : "2026-06-14T19:11:02.941", "lastUpdated" : "2026-06-15T21:26:14.712", "ingestTimestamp" : "2026-06-14T19:11:02.941", "mongoId" : "6a2c7ea474d8ee00a0953106", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ce72274d8ee00a0a6698e", "title" : "Clinical Research Coordinator", "company" : "knownwell", "industry" : "Clinical", "salary" : { "min" : 55000.0, "max" : 75000.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Schaumburg, IL", "locations" : [ "Schaumburg, IL" ], "timestamp" : "2026-06-15T22:30:21.222", "fingerprint" : "efe92001a1df5ae6d4b44b3529d072b985e833425c7f088a135d25b267d107bc", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/knownwell/e3e4dce6-aff3-4185-a7d7-09446b6bb2b7/application", "externalId" : "e3e4dce6-aff3-4185-a7d7-09446b6bb2b7", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Schaumburg", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "42.0333608,-88.0834060" } ], "locationText" : "Schaumburg, Illinois, United States", "employmentType" : "FULL_TIME", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "\uD83D\uDC4B Meet knownwell https://www.knownwell.co/, weight-inclusive healthcare for all. Join a dynamic company that is changing the way obesity care is delivered. We offer weight management, primary care, nutrition counseling, and health coaching. Our care model combines in-clinic and virtual care to bring support to patients where and when they need it. Backed by $50M in funding—including a $25M round led by CVS Health Ventures with support from a16z Bio + Health, Flare Capital, MassMutual, and Intermountain Ventures—we’re scaling fast and expanding access to evidence-based obesity care nationwide. \uD83D\uDD0D The Clinical Research Coordinator (CRC) is responsible for overseeing and coordinating all aspects of clinical trials, ensuring that studies are conducted in compliance with regulatory requirements, sponsor expectations, and Good Clinical Practice (GCP) guidelines. The CRC will act as the primary liaison between the clinical research team, patients, and external stakeholders, ensuring the efficient and timely execution of clinical research projects. Location: Schaumburg, IL On-site Requirements: Hybrid, mostly on-site. *knownwell does not offer relocation assistance* \uD83C\uDFAF What you'll do: - Study Coordination: - Coordinate and manage all aspects of clinical trials, including patient recruitment, screening, and enrollment. - Schedule and oversee patient visits, ensuring timely collection of data and samples in accordance with the study protocol. - Oversee site initiation, monitoring, closeout activities, and equipment calibration to ensure compliance with study protocols and regulations. - Maintain study documentation, including case report forms, consent forms, and other essential study records. - Review monitoring follow-up letters to ensure timely completion and resolution of identified issues. - Ensure accurate and timely reporting of adverse events (AEs) and serious adverse events (SAEs). - Manage the receipt, shipment, and storage of study drug and trial samples. - Ensure proper handling and storage of study materials, medications, and biological samples. - Generate invoices for study sponsors as applicable or assigned. Patient Interaction: - Serve as the main point of contact for participants, answering questions and providing information regarding study protocols, treatment options, and expected outcomes. - Ensure patients understand the study’s risks, benefits, and requirements by assisting in the informed consent process. - Monitor and document patient progress throughout the study, ensuring that their safety and well-being are maintained. Data Management: - Enter, maintain, and monitor study data in the clinical trial management system (CTMS) and other relevant databases. - Perform quality control checks to ensure the accuracy and completeness of data. - Collaborate with trial site staff, sponsor or CRO to resolve any discrepancies or issues with study data. Regulatory Compliance: - Stay current with federal and global regulations, including ICH-GCP and FDA guidelines, and ensure the study's adherence to applicable regulatory requirements, as well as sponsor-specific requirements. - Assist with the preparation and submission of study protocols, amendments, and regulatory documents to the Institutional Review Board (IRB). - Prepare site materials, including training materials, regulatory binders, manuals, and support documentation, ensuring alignment with regulatory guidelines and ethical standards. - Conduct training for study staff on regulatory requirements and ensure compliance with study protocols. - Maintain regulatory binders and drug accountability documents for each study. - Archive all documentation at the end of the study per Sponsor and FDA-required timelines. Study Team Collaboration: - Work closely with the Principal Investigator, Clinical Research Manager, and other research staff to ensure the study’s success. - Communicate with sponsor representatives, providing regular updates on study progress and patient enrollment. - Assist with study recruitment strategies and participate in outreach activities. \uD83C\uDF1F Who you are: - Education: - Bachelor's degree in a related field (e.g., life sciences, nursing, healthcare); CCRC Certification, and/or Master’s degree preferred. - GCP, BLS, IATA, and CSSR Certifications (or willingness to acquire if hired). Experience: - 3+ years of experience in clinical research and industry environments. 2+ years of experience with independent trial management preferred. - Solid understanding of drug development processes, FDA, and ICH GCP guidelines. - Proficiency in using multiple software systems and computer technology (preference for experience with Florence, Advarra and Greenphire). Skills: - Strong organizational, leadership, and time-management skills. - Excellent written and verbal communication skills. - Ability to work independently and as part of a multidisciplinary team. - Experience working on collaborative, diverse, and feedback-driven teams. - Proven history of adapting and thriving through periods of change. Pay & Perks: \uD83C\uDFE0\uD83C\uDFE2 Hybrid Opportunity \uD83E\uDE7A Medical, dental, and vision insurance \uD83D\uDCC8 401K retirement plan with company match \uD83C\uDFDD️ Up to 20 days of PTO per year + company holidays \uD83D\uDC76 Up to 14 weeks of parental leave (12 for non-birthing parents) \uD83C\uDFE1 Annual work from home stipend for remote employees knownwell, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Based on current size of the clinic and HIPAA regulation, providers cannot receive care in clinic and provider’s household members cannot receive primary care in the clinic. 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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. Led by Dr. Ajay Goel, Professor and Founding Chair of the Department of Molecular Diagnostics and Experimental Therapeutics, our multidisciplinary research group comprises basic researchers, gastroenterologists, surgeons, oncologists, and bioinformaticians, undertaking several collaborative projects involving large international consortia. This position has the potential to become tenure-track upon the receipt of grant funding lasting 3-5 years from a federal agency. Join us as a Clinical Research Associate, where you'll manage multiple research protocols to ensure efficiency and regulatory compliance while attending clinics as needed. You'll handle data compilation, registration, and submission, and maintain an effective system for data flow. Benefit from mentorship by experienced staff in a dynamic research environment. Our research focuses on translational studies of the genomic and epigenomic characterization of various gastrointestinal cancers (GI), including colorectal, pancreatic, gastric, esophageal, and hepatocellular cancers. Our group performs cutting-edge research in GI oncology, is very productive, and publishes in high-impact journals such as Nature Cancer, Nature Communications, Nature Biotechnology, Nature Reviews Gastroenterology and Hepatology, New England Journal of Medicine, CA: A Journal for Clinicians, Gastroenterology, Cancer Cell, PNAS, JAMA Oncology, JNCI, Cancer Research, Clinical Cancer Research, , Annals of Surgery, etc. For more information on Dr. Goel’s research, please visit here . As a successful candidate, you will: · Manages and maintains protocol documentation and regulatory documents for IRB, DSMB, and PRMC/CPRMC. · Compiles, submits, and processes data and specimens per protocol requirements, ensuring accuracy and safety. · Establishes and maintains professional relationships with patients and hospital staff while ensuring confidentiality. · Assists in patient recruitment, protocol-related tests, and evaluations, and performs protocol-specific duties. · Conducts research activities under close supervision, including laboratory experiments in microbiology, molecular biology, genetics, biochemistry, and informatics. · Identifies and communicates protocol and data management issues to the supervisor, maintains professional development, and ensures an organized work environment. Your qualifications should include: · Associate’s Degree or equivalent experience; one year in a health care setting, preferably research, with medical terminology and writing skills. · Bachelor’s Degree 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-Monrovia", "summaryDescription" : "Clinical Research Associate at City of Hope. Skills: Clinical research, Data management, Regulatory compliance. Manage research protocols. 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Our exceptional teams craft and deploy creative legal strategies that are meticulously tailored to every matter, however complex or high-stakes. The firm’s work is distinguished by a unique combination of precision and vision. Based in San Francisco, the Collaboration Services Analyst will be responsible for providing technical support to meetings and presentations involving customers and operational support for collaboration functions in the assigned GD retirement benefits; paid days off, including sick time, and vacation time; parental leave; basic life insurance; Flexible Spending Accounts; as well as discretionary, performance-based bonuses. ______ For technical difficulties with our online application, please contact us at staffrecruiting@gibsondunn.com. Our recruiting support team will respond as soon as possible. ______ Gibson Dunn is committed to ensuring equal employment opportunities for all qualified applicants, including individuals with disabilities. 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This involves maintaining protocol documentation, registering participants, compiling and submitting data, performing protocol-specific clinical duties, and managing data analyses and specimen collection.", "communicationSkills" : "medical terminology", "documentationSkills" : "protocol documentation", "qualificationsBasic" : "Associate degree (experience may substitute), ability to read, identify and extract pertinent data from medical records, and comprehend medical terminology.", "qualificationsPreferred" : "Bachelors degree, experience with medical record review, health information systems, and/or clinical trials.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. 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 Clinical Research Assistant I role is available under Dr. Saro Armenian. He directs the Center for Survivorship and Outcomes in the Hematologic Malignancies Research Institute and the Childhood, Adolescent and Young Adult Survivorship Program . You will manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance with the protocol. You will be responsible for compilation, registration and submission of data; monitor study compliance and maintain a system for effective data flow associated with research protocols. As a successful candidate, you will: · Conduct protocol management of multiple research protocols. · Maintain current and accurate protocol documentation · Ensure participants are appropriately registered and maintain documentation of participant registration. · Compile and submit data on appropriate forms according to protocol requirements. · Perform protocol specific clinical duties as required per the research study. · Perform data management and data analyses · Collect and deliver specimens for analysis Your qualifications should include: · Associates degree. Experience may substitute for minimum education requirements. Bachelors preferred. · Read, identify and extract pertinent data from medical records · Read, write and comprehend medical terminology · Experience with medical record review, health information systems, and/or clinical trials is preferred City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. 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ICH guidelines; Interventional studies", "domainList" : [ "good-clinical-practice", "ich-guidelines", "interventional-studies" ], "domainSpecificKnowledge" : [ "Good Clinical Practice", "ICH guidelines", "Interventional studies" ], "documentationSkills" : "Study documentation; Visit reports; Follow-up letters; Site documentation", "continuousLearning" : "Career development opportunities; AI-powered career advancement; Mentorship opportunities", "problemSolvingSkills" : "Issue resolution", "specialRequirements" : "Full UK right to work", "qualificationsBasic" : "6 months independent on-site monitoring experience, Experience across start-up, enrolment, maintenance, close-out, Degree in scientific discipline / health care, Equivalent industry experience, Good knowledge of GCP and ICH guidelines, Ability to establish and maintain effective working relationships, Full UK right to work", "qualificationsPreferred" : "AI tools in a professional setting confidence", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Join IQVIA on our mission to accelerate innovation for a healthier world!** IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England. **Why IQVIA?** * Career development opportunities to grow as we grow * AI‑powered career advancement through our internal talent marketplace, Career Connections * Mentorship opportunities across the organisation via Employee Resource Groups * Flexible working to assist work–life balance and professional success * Well‑being support covering your physical, mental, and financial health **Awards** * 2026 \"Glassdoor Best Place to Work in the UK\" * #1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!) * Brandon Hall Excellence Award for Learning & Development **Responsibilities** * Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines * Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability * Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues * Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase * Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements * Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation * Collaborate and liaise with study team members for project execution support as appropriate **Requirements** * Requires at least 6 months independent on-site monitoring experience of interventional studies * Experience across start-up, enrolment, maintenance, close-out * Digital literacy, including confidence using AI tools in a professional setting * Degree in scientific discipline / health care or equivalent industry experience * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines * Ability to establish and maintain effective working relationships with coworkers and clients * Full UK right to work required, this position is not eligible for visa sponsorship **Apply today and forge a career with greater purpose, make an impact, and never stop learning!** #LI-ADAMTHOMPSON 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 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.", "summaryDescription" : "Clinical Research Associate at Iqvia. Skills: Site monitoring, Clinical research, Regulatory compliance. Perform site monitoring visits. Track subject recruitment plan", "postedDate" : "2026-06-12T06:47:50.565", "createdAt" : "2026-06-12T06:47:50.539", "lastUpdated" : "2026-06-15T00:03:28.349", "ingestTimestamp" : "2026-06-12T06:47:50.539", "mongoId" : "6a2ad31774d8ee00a0714cbd", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Reading-Berkshire-United-Kingdom/Clinical-Research-Associate--South-East-England_R1550636", "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Site monitoring", "Protocol administration", "Quality evaluation", "Documentation management", "Regulatory submissions", "Mentoring", "Clinical research", "Regulatory compliance", "Regulatory requirements", "Project execution", "Good Clinical Practice", "ICH guidelines", "Interventional studies" ], "skillCount" : 13, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2c90fd74d8ee00a0981b0b", "title" : "Sr. Clinical Research Associate", "company" : "CareDx, Inc.", "industry" : "Biotech", "salary" : { "min" : 100000.0, "max" : 130000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Brisbane, California, United States", "locations" : [ "Brisbane", "California", "United States" ], "certifications" : [ "CCRC", "CCRA" ], "timestamp" : "2026-06-15T09:03:47.243", "fingerprint" : "f598ec758a847b086df5896d99fef04de8ee8149a721753c102e2868cf75425f", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/caredxinc/jobs/4260591009", "externalId" : "4260591009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Brisbane", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.6871650,-122.4027940" } ], "locationText" : "Brisbane, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Clinical study management", "Data collection", "Data reconciliation", "Site recruitment", "Clinical programming", "Data validation", "SOP development", "Workflow development", "Template development", "Timeline management", "Budget management", "Resource management", "Monitoring report execution", "Trip report execution", "Follow-up letter execution", "Site performance monitoring", "Stakeholder communication" ], "hardSkillsList" : [ "Protocol adherence", "Patient safety", "Data accuracy", "ICH/GCP compliance", "IRB requirements compliance", "Medical terminology", "Clinical trial processes" ], "softSkillsList" : [ "Leadership", "Mentoring", "Problem-solving" ], "hardSkills" : [ { "name" : "Protocol adherence", "level" : "intermediate" }, { "name" : "Patient safety", "level" : "intermediate" }, { "name" : "Data accuracy", "level" : "intermediate" }, { "name" : "ICH/GCP compliance", "level" : "intermediate" }, { "name" : "IRB requirements compliance", "level" : "intermediate" }, { "name" : "Medical terminology", "level" : "intermediate" }, { "name" : "Clinical trial processes", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" }, { "name" : "Problem-solving" } ], "majorSkills" : "Clinical research, Site management, Data integrity", "majorSkillsList" : [ "Clinical research", "Site management", "Data integrity" ], "coreResponsibilities" : "Conduct site visits, Oversee site visits, Ensure protocol adherence, Ensure patient safety, Ensure data accuracy, Collaborate with Principal Investigators, Collaborate with study coordinators, Collaborate with cross-functional teams, Ensure compliance with ICH/GCP, Ensure compliance with IRB requirements, Ensure compliance with internal monitoring plans, Identify data collection issues, Resolve data collection issues, Review data queries, Review data listings, Review data discrepancies, Reconcile data queries, Reconcile data listings, Reconcile data discrepancies, Maintain study documentation, Maintain study files, Lead study team meetings, Contribute to protocol development, Contribute to protocol amendments, Support site recruitment, Provide oversight for enrollment goals, Mentor junior CRAs, Provide technical expertise, Assist in SOP development, Assist in workflow development, Assist in template development, Partner to manage timelines, Partner to manage budgets, Partner to manage resources, Liaise with regulatory authorities, Liaise with CROs, Ensure timely execution of monitoring reports, Ensure compliant execution of monitoring reports, Ensure timely execution of trip reports, Ensure compliant execution of trip reports, Ensure timely execution of follow-up letters, Ensure compliant execution of follow-up letters, Monitor site performance metrics, Facilitate stakeholder communication", "teamCollaboration" : "Cross-functional teams; Remote teams", "projectManagementSkills" : [ "Timeline management", "Budget management", "Resource management" ], "domainKnowledge" : "Clinical research; GCP; FDA regulations; ISO standards; Medical terminology; Transplant patients", "domainList" : [ "clinical-research", "gcp", "fda-regulations", "iso-standards", "medical-terminology", "transplant-patients" ], "domainSpecificKnowledge" : [ "Clinical research", "GCP", "FDA regulations", "ISO standards", "Medical terminology", "Transplant patients" ], "toolProficiency" : [ "EDC systems", "CTMS", "Microsoft Office Suite" ], "communicationSkills" : "Interpersonal skills", "documentationSkills" : "Study documentation; Study files", "problemSolvingSkills" : "Analytical skills", "specialRequirements" : "Travel up to 75%", "qualificationsBasic" : "Bachelor’s degree or higher, 5+ years of experience, Knowledge of GCP, Knowledge of FDA regulations, Knowledge of ISO standards, Proficiency in EDC systems, Proficiency in CTMS, Proficiency in Microsoft Office Suite, Excellent understanding of medical terminology, Excellent understanding of clinical trial processes, Proven ability to manage multiple studies, Proven ability to manage priorities, Demonstrated ability to work independently, Demonstrated ability to work collaboratively, Ability to adapt quickly", "qualificationsPreferred" : "Certification (CCRC or CCRA) is a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "CareDx, Inc. is a leading precision medicine solutions company focused on the discovery, development, and commercialization of clinically differentiated, high-value healthcare solutions for transplant patients and caregivers. CareDx offers products, testing services, and digital healthcare solutions along the pre- and post-transplant patient journey, and is the leading provider of genomics-based information for transplant patients. We are seeking a highly skilled and motivated Senior Clinical Research Associate to join our Clinical Operations team. This role is pivotal in ensuring the integrity, quality, and compliance of our clinical trials. The ideal candidate will bring deep expertise in clinical study management, a passion for improving patient outcomes, and the ability to lead and mentor within a fast-paced, collaborative environment. Key Responsibilities Conduct and oversee all types of site visits (e.g., selection, initiation, interim, close-out) to ensure protocol adherence, patient safety, and data accuracy. Collaborate with Principal Investigators, study coordinators, and cross-functional teams to drive study success. Ensure compliance with ICH/GCP, IRB requirements, and internal monitoring plans. Identify and resolve data collection issues within electronic data capture (EDC) systems. Review and reconcile data queries, listings, and discrepancies. Maintain accurate and complete study documentation and files. Lead study team meetings and contribute to protocol development and amendments. Support site recruitment and provide oversight to ensure enrollment goals are met. Mentor junior CRAs and provide technical expertise in clinical programming and data validation. Assist in the development and refinement of SOPs, workflows, and templates. Partner with Clinical Trials Manager to manage timelines, budgets, and resources. Liaise with regulatory authorities and CROs as needed. Ensure timely and compliant execution of monitoring reports, trip reports, and follow-up letters. Monitor site performance metrics and facilitate effective communication across stakeholders. Qualifications Education: Bachelor’s degree or higher in biomedical sciences or a related field. Experience: 5+ years of experience in clinical research within biotech, pharma, medical device, or academia. Strong knowledge of GCP, FDA regulations, and ISO standards. Proficiency in EDC systems, CTMS, and Microsoft Office Suite. Certification (CCRC or CCRA) is a plus. Excellent understanding of medical terminology and clinical trial processes. Proven ability to manage multiple studies and priorities with precision and urgency. Exceptional communication, organizational, and interpersonal skills. Demonstrated ability to work independently and collaboratively in remote, cross-functional teams. Ability to travel up to 75% of the time. What You Bring A proactive mindset and high standards for quality and accuracy. Strong analytical and problem-solving skills. Ability to adapt quickly to changing demands and environments. A customer-focused approach in working with sites and external partners. A commitment to continuous improvement and operational excellence. Additional Details: Every individual at CareDx has a direct impact on our collective mission to improve the lives of organ transplant patients worldwide. We believe in taking great care of our people, so they take even greater care of our patients. Our competitive Total Rewards package for US Employees includes: Competitive base salary and incentive compensation Health and welfare benefits, including a gym reimbursement program 401(k) savings plan match Employee Stock Purchase Plan Pre-tax commuter benefits And more! Please refer to our page to view detailed benefits at https://caredx.com/company/careers/ In addition, we have a Living Donor Employee Recovery Policy that allows up to 30 days of paid leave annually to a full-time employee who makes the selfless act of donating an organ or bone marrow. With products that are making a difference in the lives of transplant patients today and a promising pipeline for the future, it’s an exciting time to be part of the CareDx team. Join us in partnering with transplant patients to transform our future together. CareDx, Inc. is an Equal Opportunity Employer and participates in the E-Verify program. By proceeding with our application and submitting your information, you acknowledge that you have read our U. S. Personnel Privacy Notice and consent to receive email communication from CareDx. ***We do not accept resumes from headhunters, placement agencies, or other suppliers that have not signed a formal agreement with us.*** Certain jurisdictions require notice of how we use and protect your personal information. For more information, please read our Privacy Policy. #LI-Remote This is the anticipated base salary range in the United States. 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, the type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives and restricted stock units. CareDx is a multi-state employer, and this salary range may not reflect positions that work in other states. Remote: US only roles $100,000—$130,000 USD", "summaryDescription" : "Sr. Clinical Research Associate at CareDx, Inc.. Skills: Clinical research, Site management, Data integrity. Conduct site visits. Oversee site visits", "postedDate" : "2026-06-14T04:09:17.593", "createdAt" : "2026-06-14T04:09:17.593", "lastUpdated" : "2026-06-15T09:03:47.243", "ingestTimestamp" : "2026-06-14T04:09:17.593", "mongoId" : "6a2c90fd74d8ee00a0981b0b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 100000, "salaryAnnualMax" : 130000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Protocol adherence", "Patient safety", "Data accuracy", "ICH/GCP compliance", "IRB requirements compliance", "Medical terminology", "Clinical trial processes", "Leadership", "Mentoring", "Problem-solving", "Clinical research", "Site management", "Data integrity", "Clinical study management", "Data collection", "Data reconciliation", "Site recruitment", "Clinical programming", "Data validation", "SOP development", "Workflow development", "Template development", "Timeline management", "Budget management", "Resource management", "Monitoring report execution", "Trip report execution", "Follow-up letter execution", "Site performance monitoring", "Stakeholder communication", "GCP", "FDA regulations", "ISO standards", "Transplant patients", "CCRC", "CCRA", "EDC systems", "CTMS", "Microsoft Office Suite" ], "skillCount" : 39, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2af78274d8ee00a073d5e5", "title" : "Clinical Research Associate", "company" : "AstraZeneca", "industry" : "BioPharmaceutical", "salary" : { "min" : 1200000.0, "max" : 1800000.0, "currency" : "THB", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Research Associate in Bangkok, Thailand, adjusted for the Pharmaceutical industry and a large global company." }, "location" : "Thailand", "locations" : [ "Thailand" ], "timestamp" : "2026-06-15T00:35:58.090", "fingerprint" : "0b22f2c75bb0c2a075c78ec6079cabb281802c9e5ec7ccfb732d9641749554c2", "source" : "workday", "language" : "en", "applyUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Thailand---Bangkok/Clinical-Research-Associate---BioPharmaceutical--Yearly-Contract-_R-254028", "externalId" : "R-254028", "industryFunction" : { }, "locationPoint" : "15.87,100.9925", "structuredLocations" : [ { "city" : "Bangkok", "country" : "Thailand", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "13.7524938,100.4935089" } ], "locationText" : "Bangkok, Thailand", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "professionalSkills" : [ "Study Management", "Clinical Development" ], "hardSkillsList" : [ "Regulatory inspections", "Process management" ], "hardSkills" : [ { "name" : "Regulatory inspections", "level" : "intermediate" }, { "name" : "Process management", "level" : "intermediate" } ], "majorSkills" : "Study Management, Clinical Development", "majorSkillsList" : [ "Study Management", "Clinical Development" ], "coreResponsibilities" : "Ensure processes for Study Delivery are executed, Facilitate the study delivery system, Maintain the system, Ensure delivery of a centrally managed study management, Serve as main contact, Work closely with the Document Management group, Initiate and maintain production of study documents, Ensure template and version compliance, Create or import clinical-regulatory documents, Interface with Data Management Centre representatives, Facilitate the delivery of study related documents, Manage and coordinate tracking of study materials, Monitor administrative tasks during the study process, Act as a technical owner within Patient Safety, Keep own knowledge of best practices up to, Liaise with compliance team members, Improve regulatory processes, Identify opportunities to improve methodology, Provide practical solutions for clinical development", "teamCollaboration" : "External service providers; Regulatory bodies; Study management; Other AstraZeneca employees", "projectManagementSkills" : [ "Study Management" ], "domainKnowledge" : "Clinical Development; Study Management; Patient Safety; Internal regulations", "domainList" : [ "clinical-development", "study-management", "patient-safety", "internal-regulations" ], "domainSpecificKnowledge" : [ "Clinical Development", "Study Management", "Patient Safety", "Internal regulations" ], "toolProficiency" : [ "Global Electronic Library" ], "documentationSkills" : "Study reports; Study documents; Clinical-regulatory documents", "continuousLearning" : "Keep own knowledge of best practices and new relevant developments up to date", "innovationCreativity" : "Identifies opportunities to improve the methodology; Provide practical solutions for clinical development", "problemSolvingSkills" : "Provide practical solutions", "qualificationsBasic" : "Bachelor’s degree in relevant, Experience of Study Management within a pharmaceutical or clinical, Knowledge of relevant legislation and new developments in the area of Clinical Development and Study Management", "qualificationsPreferred" : "Advanced degree within the Professional, Understanding of multiple aspects within Study Management", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Typical Accountabilities: • Ensures the processes for Study Delivery are executed through the development of study reports tools, facilitation of the study delivery system and maintenance of the system. • As an expert, ensures delivery of a centrally managed study management service across clinical studies from start up to reporting • Serve as main contact and works closely with the Document Management group until the Clinical Study Report is finalised • Initiates and maintains production of study documents, ensuring template and version compliance • Creates or imports clinical-regulatory documents into the Global Electronic Library according to the Global Document List • Interfaces with Data Management Centre or Data Management Enablement representatives to facilitate the delivery of study related documents • Manages and coordinates tracking of study materials and equipment • Monitors administrative tasks during the study process, audits and regulatory inspections, according to company policies • Acts as a technical owner within Patient Safety with a deep understanding of processes and internal regulations • Keeps own knowledge of best practices and new relevant developments up to date • Liaises with compliance team members to improve regulatory processes within the team • Identifies opportunities to improve the methodology and provide practical solutions for clinical development Typical People Management Responsibility (direct / indirect reports): • Approximate number of people managed in total (all levels) - None What is the global remit? (how many countries will the role operate in?): • Own country Education, Qualifications, Skills and Experience: • Essential: Bachelor’s degree in relevant discipline; Experience of Study Management within a pharmaceutical or clinical background; Knowledge of relevant legislation and new developments in the area of Clinical Development and Study Management • Desirable: Advanced degree within the field; Professional certification; Understanding of multiple aspects within Study Management Key Relationship to reach solutions: • Internal (to AZ or team): Study management function; Other AstraZeneca employees • External (to AZ): External service providers and regulatory bodies **Date Posted** 11-Jun-2026 **Closing Date** 30-Jul-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 Research Associate at AstraZeneca. Skills: Study Management, Clinical Development. Ensure processes for Study Delivery are executed. Facilitate the study delivery system", "postedDate" : "2026-06-12T04:58:28.906", "createdAt" : "2026-06-12T04:58:28.889", "lastUpdated" : "2026-06-15T00:35:58.090", "ingestTimestamp" : "2026-06-12T04:58:28.889", "mongoId" : "6a2af78274d8ee00a073d5e5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Thailand---Bangkok/Clinical-Research-Associate---BioPharmaceutical--Yearly-Contract-_R-254028", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Regulatory inspections", "Process management", "Study Management", "Clinical Development", "Patient Safety", "Internal regulations", "Global Electronic Library" ], "skillCount" : 7, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "BioPharmaceutical" }, { "id" : "6a2ad31774d8ee00a0714cc0", "title" : "Clinical Research Associate", "company" : "Iqvia", "industry" : "Healthcare", "salary" : { "min" : 45000.0, "max" : 65000.0, "currency" : "GBP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Research Associate in Bath, United Kingdom, adjusted for the Biotech industry and company size." }, "location" : "Bath, United Kingdom", "locations" : [ "Bath, United Kingdom" ], "timestamp" : "2026-06-14T23:31:06.216", "fingerprint" : "697a8aabea8053df9f8ee72012d016429352818385a0904d81621156d67e72a2", "source" : "workday", "language" : "en", "applyUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Bath-United-Kingdom/Clinical-Research-Associate--South-West-England_R1550620", "externalId" : "R1550620", "industryFunction" : { }, "locationPoint" : "51.3751,-2.36172", "structuredLocations" : [ { "city" : "Bath", "country" : "United Kingdom", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "51.3813864,-2.3596963" } ], "locationText" : "Bath, United Kingdom", "employmentType" : "FULL_TIME", "technicalSkills" : "AI", "professionalSkills" : [ "Clinical research", "Site monitoring", "Regulatory requirements", "Protocol management", "Data query resolution", "Site documentation" ], "hardSkillsList" : [ "Site monitoring", "Protocol training", "Quality evaluation", "Regulatory submissions", "Data query resolution", "Visit reports", "Follow-up letters" ], "softSkillsList" : [ "Mentorship" ], "hardSkills" : [ { "name" : "Site monitoring", "level" : "intermediate" }, { "name" : "Protocol training", "level" : "intermediate" }, { "name" : "Quality evaluation", "level" : "intermediate" }, { "name" : "Regulatory submissions", "level" : "intermediate" }, { "name" : "Data query resolution", "level" : "intermediate" }, { "name" : "Visit reports", "level" : "intermediate" }, { "name" : "Follow-up letters", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Mentorship" } ], "majorSkills" : "Site monitoring, Clinical research, Regulatory compliance", "majorSkillsList" : [ "Site monitoring", "Clinical research", "Regulatory compliance" ], "coreResponsibilities" : "Perform site monitoring visits, Work with sites to adapt recruitment plan, Administer protocol and related study training, Establish regular lines of communication with sites, Evaluate quality and integrity of study site practices, Escalate quality issues, Manage progress of assigned studies, Track regulatory submissions and approvals, Track recruitment and enrollment, Track case report form completion, Track data query generation and resolution, Support start-up phase, Ensure site documents are available for filing, Verify Investigator's Site File maintenance, Create and maintain documentation regarding site management, Submit regular visit reports, Generate follow-up letters, Collaborate and liaise with study team members", "teamCollaboration" : "Study team members", "domainKnowledge" : "Good Clinical Practice; ICH guidelines; Interventional studies", "domainList" : [ "good-clinical-practice", "ich-guidelines", "interventional-studies" ], "domainSpecificKnowledge" : [ "Good Clinical Practice", "ICH guidelines", "Interventional studies" ], "documentationSkills" : "Study documentation; Visit reports; Follow-up letters", "continuousLearning" : "Career development opportunities; AI-powered career advancement; Mentorship opportunities", "specialRequirements" : "25% travel", "qualificationsBasic" : "6 months independent on-site monitoring experience, Experience across start-up, enrolment, maintenance, close-out, Digital literacy, including confidence using AI tools, Degree in scientific discipline / health care or equivalent industry experience, Good knowledge of, and skill in applying, applicable clinical research regulatory requirements, Ability to establish and maintain effective working relationships, Full UK right to work", "qualificationsPreferred" : "AI-powered career advancement experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Join IQVIA on our mission to accelerate innovation for a healthier world!** IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South West England. **Why IQVIA?** * Career development opportunities to grow as we grow * AI‑powered career advancement through our internal talent marketplace, Career Connections * Mentorship opportunities across the organisation via Employee Resource Groups * Flexible working to assist work–life balance and professional success * Well‑being support covering your physical, mental, and financial health **Awards** * 2026 \"Glassdoor Best Place to Work in the UK\" * #1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!) * Brandon Hall Excellence Award for Learning & Development **Responsibilities** * Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines * Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability * Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues * Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase * Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements * Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation * Collaborate and liaise with study team members for project execution support as appropriate **Requirements** * Requires at least 6 months independent on-site monitoring experience of interventional studies * Experience across start-up, enrolment, maintenance, close-out * Digital literacy, including confidence using AI tools in a professional setting * Degree in scientific discipline / health care or equivalent industry experience * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines * Ability to establish and maintain effective working relationships with coworkers and clients * Full UK right to work required, this position is not eligible for visa sponsorship **Apply today and forge a career with greater purpose, make an impact, and never stop learning!** #LI-ADAMTHOMPSON 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 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.", "summaryDescription" : "Clinical Research Associate at Iqvia. Skills: Site monitoring, Clinical research, Regulatory compliance. Perform site monitoring visits. 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Laboratory leadership", "domainKnowledge" : "Clinical laboratory testing; FACT; AABB; ACHI; CAP; FDA; Joint Commission; CLIA 1988", "domainList" : [ "clinical-laboratory-testing", "fact", "aabb", "achi", "cap", "fda", "joint-commission", "clia-1988" ], "domainSpecificKnowledge" : [ "Clinical laboratory testing", "FACT", "AABB", "ACHI", "CAP", "FDA", "Joint Commission", "CLIA 1988" ], "documentationSkills" : "Proper documentation", "problemSolvingSkills" : "Troubleshooting", "qualificationsBasic" : "High-complexity clinical laboratory testing, FACT compliance, AABB compliance, ACHI compliance, CAP compliance, FDA compliance, Joint Commission compliance, CLIA 1988 compliance", "qualificationsPreferred" : "Continued growth in test system analysis, Continued growth in troubleshooting, Continued growth in regulatory proficiency", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "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. This role involves preparing specimens and performing waived to high‑complexity clinical laboratory testing in full compliance with SOPs and all major regulatory standards, including FACT, AABB, ACHI, CAP, FDA, and Joint Commission requirements. The position supports education by assisting in training students and staff, while also demonstrating continued growth in test system analysis, troubleshooting, and regulatory proficiency. It requires a strong understanding of section operations, contributions to staff development and future testing needs, and serving as a technical resource for laboratory personnel and leadership. All work is performed under the authorization of the Laboratory Director in accordance with CLIA 1988 (CFR 493.1445(a)). As a successful candidate, you will: Maintain strong technical proficiency in specimen processing, laboratory testing, equipment operation, and accurate result reporting. Perform and document quality control, quality assurance, and performance improvement activities, including troubleshooting and resolving complex technical issues. Prepare reagents and materials, ensure proper documentation, follow safety protocols, and uphold high standards of integrity and customer service. Draft, revise, validate, and ensure compliance of laboratory policies, procedures, SOPs, and accreditation requirements. Lead or support validation of new instruments, reagents, and tests; analyze data; and participate in inspections, proficiency testing, and regulatory readiness. Oversee workflow, scheduling, staff competency, and quality performance indicators while identifying improvement opportunities and supporting departmental operations. Your qualifications should include: Bachelor’s Degree Minimum 5 years as a certified or licensed clinical laboratory scientist Clinical Laboratory Scientist 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 Laboratory Scientist Lead - Clinical Research at City of Hope. Skills: Clinical laboratory testing, Quality assurance, Regulatory compliance. Prepare specimens. Perform clinical laboratory testing", "createdAt" : "2026-06-14T06:26:43.012", "lastUpdated" : "2026-06-15T11:39:41.135", "ingestTimestamp" : "2026-06-14T06:26:43.012", "mongoId" : "6a1a5cd658b93c861e80fa69", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 115500, "salaryAnnualMax" : 165000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Specimen processing", "Laboratory testing", "Equipment operation", "Result reporting", "Quality control", "Quality assurance", "Performance improvement", "Reagent preparation", "Clinical laboratory testing", "Regulatory compliance", "Test system analysis", "Troubleshooting", "Regulatory proficiency", "Staff development", "Technical resource", "FACT", "AABB", "ACHI", "CAP", "FDA", "Joint Commission", "CLIA 1988" ], "skillCount" : 22, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Lead", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69fd34b84c40e2acd1b2f5ed", "title" : "Clinical Research Nurse-Lymphoma", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 85000.0, "max" : 115000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Clinical Research Nurse in Duarte, California, adjusted for mid-seniority and the healthcare industry." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Clinical Trials Operations", "Onsite, Days, Days" ], "certifications" : [ "RN license", "BLS certification" ], "timestamp" : "2026-06-16T02:13:03.590", "fingerprint" : "d5f495f0341b554ccb0be9dde0bf4f402b6850a4fbb731266d9e7446f5829d69", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=229444", "externalId" : "229444", "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" : 2, "technicalSkills" : "Epic", "professionalSkills" : [ "Clinical documentation", "Patient care" ], "hardSkillsList" : [ "Patient assessment", "Medication administration" ], "hardSkills" : [ { "name" : "Patient assessment", "level" : "intermediate" }, { "name" : "Medication administration", "level" : "intermediate" } ], "majorSkills" : "Clinical research, Lymphoma", "majorSkillsList" : [ "Clinical research", "Lymphoma" ], "coreResponsibilities" : "Provide direct patient care, Administer medications, Monitor patient status, Educate patients and families, Document patient care, Participate in clinical research, Adhere to safety protocols, Collaborate with healthcare team", "teamCollaboration" : "Healthcare team", "domainKnowledge" : "Lymphoma; Clinical trials; HIPAA", "domainList" : [ "lymphoma", "clinical-trials", "hipaa" ], "domainSpecificKnowledge" : [ "Lymphoma", "Clinical trials", "HIPAA" ], "toolProficiency" : [ "Epic EHR" ], "communicationSkills" : "Patient education", "documentationSkills" : "Clinical documentation", "qualificationsBasic" : "2 years experience", "qualificationsPreferred" : "Epic certification preferred, Oncology experience preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "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. Are you a compassionate and detail-oriented Registered Nurse passionate about advancing healthcare? Join our team as a Clinical Research Nurse , where you’ll play a vital role in guiding patients through innovative clinical trials while collaborating with a multidisciplinary team of physicians, Clinical Research Associates (CRA), pharmacists, and coordinators. This is a unique opportunity to blend clinical expertise with research excellence—helping bring groundbreaking treatments to life while delivering exceptional patient-centered care. What You’ll Do Clinical Trial Patient Management Partner with investigators to determine patient eligibility and ensure accurate documentation of clinical trial criteria Assess, monitor, and document patient conditions, treatment responses, and changes in health status in accordance with IRB protocols Coordinate care across the continuum (outpatient, inpatient, and home settings) Triage patient calls and provide proactive communication and support to patients and families Collaborate closely with physicians, nurse practitioners (NPs), physician assistants (PAs), pharmacists, and research teams Plan and execute protocol-specific activities including randomization, assessments, treatments, and follow-ups Ensure all clinical trial documentation is complete, accurate, and compliant to avoid protocol deviations Support and monitor patient adherence to study protocols Patient & Family Education Educate patients and families on clinical trial treatments, procedures, and follow-up care Provide ongoing support to ensure understanding and adherence to treatment plans Informed Consent & Compliance Ensure informed consent processes meet all regulatory requirements (IRB, FDA, institutional, and sponsor guidelines) Participate in patient education during consent and escalate concerns to the Principal Investigator Maintain timely and accurate documentation of consent forms Protocol Oversight & Collaboration Assist with study initiation, monitoring visits, and audits Collaborate with research pharmacy and investigators to develop and implement protocol-specific orders Promote adherence to clinical trial protocols and regulatory standards Coordinate scheduling of patient visits, testing, and follow-ups Educate nursing staff on protocol requirements and safe medication administration Additional Responsibilities Deliver patient-centered care in alignment with organizational policies and the California Nurse Practice Act Maintain a high standard of professionalism, teamwork, and organization Stay current with clinical research regulations, standards, and best practices Serve as a mentor or preceptor for new staff and nursing students Collaborate with internal teams and external partners including physicians, sponsors, and community resources Full time 10 hour days / 40 hour week Your qualifications should include: BSN 2 or more years of experience in oncology. clinical research, research, ICU, other intensive care setting, pediatrics, case management or nurse navigation. Human subjects protection training (can be completed after hire) Required Certification/Licensure: Current California RN License American Heart Association BLS Certification 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 Research Nurse-Lymphoma at City of Hope. Skills: Clinical research, Lymphoma. Provide direct patient care. Administer medications", "createdAt" : "2026-06-14T20:49:19.086", "lastUpdated" : "2026-06-16T02:13:03.590", "ingestTimestamp" : "2026-06-14T20:49:19.086", "mongoId" : "69fd34b84c40e2acd1b2f5ed", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 85000, "salaryAnnualMax" : 115000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Patient assessment", "Medication administration", "Clinical research", "Lymphoma", "Clinical documentation", "Patient care", "Clinical trials", "HIPAA", "RN license", "BLS certification", "Epic EHR" ], "skillCount" : 11, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2a73d574d8ee00a0651721", "title" : "Clinical Research Specialist- External Research Program (ERP)", "company" : "Medtronic", "industry" : "Healthcare", "salary" : { "min" : 52800.0, "max" : 79200.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : false }, "location" : "Maastricht, Limburg, Netherlands", "locations" : [ "Maastricht, Limburg, Netherlands" ], "timestamp" : "2026-06-13T08:46:35.899", "fingerprint" : "b0b948a5d91e31c2fa045f018bbfda67ab8abcd55971748cd733ed7bb8a04355", "source" : "workday", "language" : "en", "applyUrl" : "https://medtronic.wd1.myworkdayjobs.com/MedtronicCareers/job/Maastricht-Limburg-Netherlands/Clinical-Research-Specialist--External-Research-Program--ERP-_R68235", "externalId" : "R68235", "industryFunction" : { }, "locationPoint" : "50.84833,5.68889", "structuredLocations" : [ { "city" : "Maastricht", "state" : "Limburg", "country" : "Netherlands", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "50.8512438,5.6909768" } ], "locationText" : "Maastricht, Limburg, Netherlands", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "professionalSkills" : [ "Investigator-initiated research", "Clinical research operations", "Financial management", "Portfolio reviews" ], "hardSkillsList" : [ "Cardiac rhythm management", "Contracting" ], "hardSkills" : [ { "name" : "Cardiac rhythm management", "level" : "intermediate" }, { "name" : "Contracting", "level" : "intermediate" } ], "majorSkills" : "External research program, Investigator-initiated studies, Clinical research", "majorSkillsList" : [ "External research program", "Investigator-initiated studies", "Clinical research" ], "coreResponsibilities" : "Support execution of External Research Program portfolio, Serve as operational point of contact, Coordinate ERP lifecycle activities, Track documentation, timelines, and milestones, Partner with cross functional stakeholders, Facilitate review of ERP proposals, Support ERP agreements and amendments, Lead financial management of portfolio, Forecast payments, Process payment requests, Manage accruals, Communicate with cost center owners, Monitor study progress, Identify risks, Identify data gaps, Identify documentation gaps, Escalate issues, Conduct portfolio reviews, Liaise on fair market value evaluation, Liaise on contracting, Align terms with operational requirements, Align terms with compliance requirements, Contribute to continuous improvement of ERP tools, Contribute to continuous improvement of ERP templates, Contribute to continuous improvement of ERP workflows, Share learnings across clinical organization, Share best practices across clinical organization, Share learnings across enterprise ERP community, Share best practices across enterprise ERP community, Embrace responsible hyperautomation use, Embrace responsible AI use, Operate with a global mindset, Support ERPs in various countries, Keep in mind cultural norms, Keep in mind cultural expectations, Build optimal relationships, Maintain optimal relationships, Foster effective collaborations", "teamCollaboration" : "Cross functional stakeholders; Medical scientific advisors; Local clinical teams; Internal and external parties", "domainKnowledge" : "Cardiac rhythm management; External research program", "domainList" : [ "cardiac-rhythm-management", "external-research-program" ], "domainSpecificKnowledge" : [ "Cardiac rhythm management", "External research program" ], "communicationSkills" : "Presenting to physicians", "innovationCreativity" : "Innovation", "problemSolvingSkills" : "Creative problem solving", "qualificationsBasic" : "Bachelors in biological science or biomedical engineering, Experience in clinical or laboratory research, Worked in a clinical cardiac setting, Detail oriented, Comfortable presenting to small audiences, Ability to influence colleagues, English fluency", "qualificationsPreferred" : "Master's degree in biological science or biomedical engineering, Additional languages, Aptitude for creative problem solving, Scientific background in Cardiac Rhythm Management, Customer-facing background in Cardiac Rhythm Management", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. # **A Day in the Life** Seeking a dynamic individual interested in advancing the cardiac rhythm management (CRM) operating unit (OU) via support of our external research program (ERP). Ideal role for a candidate that has a keen interest in investigator-initiated research operations on a global scale, with room to grow into some scientific responsibility in the future. **Responsibilities may include the following and other duties may be assigned:** * Support execution of the External Research Program (ERP) portfolio by serving as an operational point of contact for investigator initiated studies and coordinate ERP lifecycle activities (from review through close out) in alignment with Medtronic ERP policy and applicable procedures, ensuring documentation, timelines, and milestones are tracked appropriately * Partner with cross functional stakeholders (e.g., R&T, Clinical, Legal, Compliance, and Finance, etc.) to facilitate review and support of ERP proposals, agreements, and amendments * Lead effective financial management of portfolio, inclusive of forecasting, payment requests, accruals, and proactive communication to cost center owners/stakeholders * Monitor study progress through appropriate tracking tools, proactively identifying risks, data or documentation gaps, and escalating issues per defined processes and conduct routine portfolio reviews with medical scientific advisors, and/or local clinical teams to align on study progress, status, and any watch outs * Liaise with local team or MCRS on fair market value evaluation and contracting, aligning agreed upon terms with operational and compliance requirements and contribute to continuous improvement of ERP tools, templates, and workflows, sharing learnings and best practices across the clinical organization and enterprise ERP community * Embrace responsible hyperautomation and AI use in daily work and operate with a global mindset, supporting ERPs in various countries, keeping in mind cultural norms and expectations * Builds and maintains optimal relationships and effective collaborations with various internal and external parties **Required Knowledge and Experience:** * Bachelors in biological science or biomedical engineering and experience in clinical or laboratory research and/or worked in a clinical cardiac setting * Detail oriented and comfortable presenting to small audiences, including physicians * Ability to influence colleagues of all levels, on both content and timelines * English fluency A master’s degree in biological science or biomedical engineering, additional languages, aptitude for creative problem solving and scientific and/or customer-facing background in Cardiac Rhythm Management are considered an advantage for this role. **Physical Job Requirements** The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. # **Benefits & Compensation** **Medtronic offers a competitive Salary and flexible Benefits Package** A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Netherlands: 52,800.00 EUR - 79,200.00 EUR | This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). # **About Medtronic** # We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity [here](http://www.medtronic.com)", "summaryDescription" : "Clinical Research Specialist- External Research Program (ERP) at Medtronic. Skills: External research program, Investigator-initiated studies, Clinical research. Support execution of External Research Program portfolio. 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Our mission is to drive meaningful innovation in healthcare, improving clinical practice and patients’ quality of life. With over 300 professionals , we deliver end-to-end solutions across clinical research, patient support programs, medical education, and healthcare communication. We’re currently looking for a proactive Clinical Research Associate (CRA) to join our Clinical Operations team in a hybrid role (Milan-based) . Prerequisite What you’ll do Ensure studies are conducted in compliance with protocols, GCP, and regulations Perform site visits (selection, initiation, monitoring, close-out) Oversee patient recruitment, CRF completion, and query management Support sites and manage communication with external vendors Ensure accurate AE reporting and manage protocol deviations Maintain study documentation and files Collaborate across teams and support site payments What we’re looking for ·Degree in life sciences (Pharmacy, Biology, Biochemistry, or related) Certification in accordance with the Italian Ministerial Decree of November 15, 2011. Strong knowledge of GCP and clinical trial regulations Excellent English (additional languages a plus) Availability to travel across Italy A dynamic, organized, and proactive mindset What we offer Permanent contract Hybrid working model Continuous training & development Competitive compensation Real career growth opportunities Supportive and collaborative environment Location: Milan HQ (Hybrid) Ready to make an impact in clinical research? Apply now or reach out to learn more! What are we expecting from you?", "summaryDescription" : "Clinical Research Associate (CRA) at Evidenze. Skills: Clinical research, GCP compliance, Site monitoring. Ensure studies compliance. Perform site visits", "createdAt" : "2026-06-14T00:35:21.210", "lastUpdated" : "2026-06-15T07:43:28.192", "ingestTimestamp" : "2026-06-14T00:35:21.210", "mongoId" : "6a2c72a274d8ee00a09314e7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Site visits", "Patient recruitment", "CRF completion", "Query management", "AE reporting", "Protocol deviations", "Study documentation", "Proactive mindset", "Clinical research", "GCP compliance", "Site monitoring", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "GCP", "Clinical trial regulations", "Certification in accordance with the Italian Ministerial Decree of November 15, 2011" ], "skillCount" : 21, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a454e74d8ee00a05d1966", "title" : "Clinical Research Associate", "company" : "Resilience", "industry" : "Medical", "salary" : { "min" : 42000.0, "max" : 55000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Clinical Research Associate in Paris, France, adjusted for the biotech industry and company size." }, "location" : "Paris", "locations" : [ "Paris", "Biarritz", "Bordeaux", "Grenoble", "Lyon", "Toulouse" ], "certifications" : [ "CRA certification", "Clinical Research certification" ], "timestamp" : "2026-06-14T22:16:11.833", "fingerprint" : "04cbed1297e7107d0c591b3cb3a4a0fcfb941dc2d64f8094df043a0293aa9643", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/Resilience%20Care/f732f7ad-7189-4ed4-a203-ab0e642f6202/application", "externalId" : "f732f7ad-7189-4ed4-a203-ab0e642f6202", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Paris", "country" : "France", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "48.8534951,2.3483915" } ], "locationText" : "Paris, France", "employmentType" : "TEMPORARY", "minimumEducation" : "Bachelor's", "professionalSkills" : [ "Clinical research", "Site operations" ], "hardSkillsList" : [ "Protocol deviation tracking", "CAPA management", "eTMF completeness" ], "softSkillsList" : [ "Rigorous", "Organized", "Agile environments" ], "hardSkills" : [ { "name" : "Protocol deviation tracking", "level" : "intermediate" }, { "name" : "CAPA management", "level" : "intermediate" }, { "name" : "eTMF completeness", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Rigorous" }, { "name" : "Organized" }, { "name" : "Agile environments" } ], "majorSkills" : "Site monitoring, Data quality, Clinical execution", "majorSkillsList" : [ "Site monitoring", "Data quality", "Clinical execution" ], "coreResponsibilities" : "Conduct site monitoring visits, Ensure quality of clinical data, Ensure completeness of clinical data, Ensure quality of eCRFs, Ensure completeness of eCRFs, Track protocol deviations, Manage CAPA, Own eTMF completeness, Monitor recruitment metrics, Oversee timely query resolution, Serve as operational contact for sites, Contribute to site feasibility, Contribute to site qualification, Support visit planning, Coordinate with internal teams, Coordinate with vendors, Participate in study meetings, Follow-up on actions, Implement tracking tools, Implement dashboards, Implement internal process documentation, Contribute to continuous improvement, Share operational insights", "teamCollaboration" : "Collaborative environment; Agile environments", "domainKnowledge" : "ICH-GCP; Clinical site operations", "domainList" : [ "ich-gcp", "clinical-site-operations" ], "domainSpecificKnowledge" : [ "ICH-GCP", "Clinical site operations" ], "toolProficiency" : [ "eCRFs", "eTMF" ], "communicationSkills" : "Clear communication; Professional relationships", "documentationSkills" : "Internal process documentation", "continuousLearning" : "Grow expertise", "innovationCreativity" : "Innovative studies; Digital products; AI-powered tools", "specialRequirements" : "Travel ~40% of time, Travel across France, Travel across Europe", "qualificationsBasic" : "CRA or Clinical Research certification, First experience or internship in clinical research, Good knowledge of ICH-GCP, Knowledge of clinical site operations, Fluency in French, Fluency in English, Valid driving license", "qualificationsPreferred" : "Scientific or paramedical degree, Master's degree, DU FIEC degree, Willingness to travel", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "1️⃣ WHAT YOU'LL BE DOING \uD83D\uDCDD Your job In a few words As a Clinical Research Associate (CRA) at Resilience under a 1-year fixed-term contract (CDD), you will join a committed, fast-growing, and agile team at the forefront of digital, patient-centered clinical research. You will be directly involved in monitoring and managing ambitious multicenter studies across several therapeutic areas. You will play a key role in ensuring quality and compliance at every stage of clinical execution. This is a hands-on role offering strong exposure, autonomy, and the opportunity to grow within a collaborative and impact-driven environment. Your day-to-day responsibilities - Conduct site monitoring visits (initiation, routine, close-out) according to study plans - Ensure quality and completeness of clinical data and eCRFs - Protocol deviation tracking & CAPA management - eTMF completeness ownership - Monitor recruitment metrics and oversee timely query resolution - Serve as the key operational contact for investigator sites - Site feasibility & qualification contribution - Support visit planning and coordination with internal teams and vendors - Actively participate in study meetings and follow-up actions - Help implement tracking tools, dashboards, and internal process documentation - Contribute to continuous improvement efforts and share operational insights with the team 2️⃣ What You'll Bring ⚙️ You definitely have - A scientific or paramedical degree (Bachelor’s, Master’s, DU FIEC or equivalent) - A CRA or Clinical Research certification - A first experience or strong internship in clinical research - A good knowledge of ICH-GCP and clinical site operations - Fluency in French and English (oral and written) - A valid driving license and willingness to travel (~40% of your time across France and Europe \uD83D\uDE42 You’re the right person if you - Are rigorous, organized, and proactive - Communicate clearly and build strong professional relationships - Know how to manage multiple priorities at once - Want to grow your expertise while working on innovative, high-impact clinical studies - Thrive in agile and collaborative environments - Are genuinely excited about digital products and AI-powered tools 3️⃣ Recruitment Interview 1 with Elena (20min) Interview 2 with Anne-Julie Eve, Clinical Operations Lead – Introduction and motivation (30min) Interview 3 - Case Study with Anne-Julie, Agathe Combes, Ayelen Gallardo (45min) Interview 4 with Blanche Berneron GDPR : Your personal data will be processed for the purposes of recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. They will be available only for people involved in the process and erased after 2 years of inactivity. Under GDPR and as Resilience attach great importance to privacy, please note that you have the right to request access to your personal data, to request that your personal data be rectified or erased. The Data Protection Officer can be contacted at privacy@resilience.care For more information, please check our privacy policy https://patients.resilience.care/politique-de-confidentialite.", "summaryDescription" : "Clinical Research Associate at Resilience. Skills: Site monitoring, Data quality, Clinical execution. Conduct site monitoring visits. Ensure quality of clinical data", "postedDate" : "2026-06-11T18:16:30.667", "createdAt" : "2026-06-11T18:16:30.667", "lastUpdated" : "2026-06-14T22:16:11.833", "ingestTimestamp" : "2026-06-11T18:16:30.667", "mongoId" : "6a2a454e74d8ee00a05d1966", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Protocol deviation tracking", "CAPA management", "eTMF completeness", "Rigorous", "Organized", "Agile environments", "Site monitoring", "Data quality", "Clinical execution", "Clinical research", "Site operations", "ICH-GCP", "Clinical site operations", "CRA certification", "Clinical Research certification", "eCRFs", "eTMF" ], "skillCount" : 17, "jobCategory" : "other", "jobSubcategory" : "medical---clinical-ops", "dataQualityScore" : 0.8888889, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2a5cee74d8ee00a06172d1", "title" : "Clinical Research Coordinator", "company" : "Care Access", "industry" : "Healthcare", "salary" : { "min" : 48000.0, "max" : 65000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for a Junior Clinical Research Coordinator in Louisiana, United States, with adjustments for the healthcare industry and company size." }, "location" : "Louisiana, United States", "locations" : [ "Louisiana", "United States" ], "certifications" : [ "National phlebotomy certification" ], "timestamp" : "2026-06-14T22:14:07.097", "fingerprint" : "ab96b18c06b2fe3db4c850a6a15d6d85270582b7dabc914ee01c23c9efc60b2c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/careaccess/jobs/4280447009", "externalId" : "4280447009", "industryFunction" : { }, "structuredLocations" : [ { "state" : "Louisiana", "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "Louisiana, United States", "technicalSkills" : "MS Word, MS Excel", "professionalSkills" : [ "Medical terminology", "Research terminology", "Clinical documentation" ], "hardSkillsList" : [ "Phlebotomy", "ECGs", "Vital signs" ], "softSkillsList" : [ "Critical thinker", "Problem solver", "Adaptability" ], "hardSkills" : [ { "name" : "Phlebotomy", "level" : "intermediate" }, { "name" : "ECGs", "level" : "intermediate" }, { "name" : "Vital signs", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Critical thinker" }, { "name" : "Problem solver" }, { "name" : "Adaptability" } ], "majorSkills" : "Good Clinical Practices, Protocol compliance, Patient monitoring", "majorSkillsList" : [ "Good Clinical Practices", "Protocol compliance", "Patient monitoring" ], "coreResponsibilities" : "Screen study subjects, Enroll study subjects, Monitor study subjects, Ensure protocol compliance, Ensure regulatory compliance, Obtain informed consent, Follow SOPs/GCP, Complete documentation accurately, Follow patient privacy protocols, Follow patient safety protocols, Complete visit procedures, Complete basic clinical procedures, Perform blood draws, Record vital signs, Perform ECGs, Review laboratory results, Review ECGs, Review test results, Alert value notification, Ensure investigator review, Discuss study medication, Discuss required procedures, Discuss eligibility criteria, Discuss impact on office flow, Prioritize activities, Maintain adherence to FDA regulations, Maintain adherence to ICH guidelines, Coordinate pre-study visits, Coordinate site initiation visits, Coordinate monitor visits, Identify adverse events, Identify Serious Adverse Events, Notify Principal Investigator, Notify Sponsor, Record data legibly, Enter data in real time, Record study medication inventory, Record medication dispensation, Record patient compliance, Resolve data management queries, Correct source data, Assist regulatory personnel, Assist with filing regulatory documents, Assist in creation of source documents, Assist in review of source documents, Assist with recruitment materials, Assist in development of recruitment plan, Obtain listing of potential candidates, Call participants, Recruit participants, Review protocol, Assess protocol amendments, Ensure training requirements met, Ensure study requirements met, Communicate clearly verbally, Communicate clearly in writing, Attend Investigator meetings, Escalate issues, Own assigned tasks, Meet deadlines, Ensure adequate supplies arrived, Interact professionally with patients, Interact professionally with sponsor representatives, Interact professionally with investigators, Interact professionally with personnel, Maintain effective relationships with participants, Maintain effective relationships with personnel", "teamCollaboration" : "Work with diverse team; Work with site staff; Work with Sponsor/CRO; Work with recruitment team; Work with clinical staff; Work with management", "projectManagementSkills" : [ "Prioritization", "Organization" ], "domainKnowledge" : "Good Clinical Practices; FDA regulations; ICH guidelines; Clinical trials", "domainList" : [ "good-clinical-practices", "fda-regulations", "ich-guidelines", "clinical-trials" ], "domainSpecificKnowledge" : [ "Good Clinical Practices", "FDA regulations", "ICH guidelines", "Clinical trials" ], "toolProficiency" : [ "Clinical trials database", "IVR systems", "Electronic data capture" ], "communicationSkills" : "Verbal communication; Written communication; Professional communication", "documentationSkills" : "Source document creation; Regulatory document filing", "problemSolvingSkills" : "Problem solver; Critical thinker", "specialRequirements" : "Onsite work 5 days, Up to 10% travel, Lifting up to 25 lbs, Walking, Standing, Sitting, Driving", "qualificationsBasic" : "1-year prior Clinical Research Coordinator experience, Recent phlebotomy experience, National phlebotomy certification", "qualificationsPreferred" : "Bachelor's Degree preferred, Epic certification preferred", "workSiteFlexibility" : "Onsite", "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 Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance. How You'll Make An Impact Patient Coordination Prescreen study candidates   Obtain informed consent per Care Access Research SOP .  Follows SOPs/GCP precisely; completes documentation accurately. Demonstrates empathy; follows patient privacy and safety protocols. Complete visit procedures in accordance with protocol.  Complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.  Receives structured mentorship; participates in shadowing and skills validation. Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.  Low complexity; stable protocols with limited procedures and minimal IP handling. Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.  Prioritize activities with specific regard to protocol timelines  Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.  Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.  Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate) Documentation Record data legibly and enter in real time on paper or e-source documents   Accurately record study medication inventory, medication dispensation, and patient compliance.  Resolve data management queries and correct source data within sponsor provided timelines  Assist regulatory personnel with completion and filing of regulatory documents.  Assist in the creation and review of source documents.  Patient Recruitment Assist with planning and creation of appropriate recruitment materials.  Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database.  Actively work with recruitment team in calling and recruiting participants Other Responsibilities Review and assess protocol (including amendments) for clarity, logistical feasibility Ensure that all training and study requirements are met prior to trial conduct.  Communicate clearly verbally and in writing.  Attend Investigator meetings as required.   Adapts to new systems; seeks feedback; escalates issues. Owns assigned tasks; meets deadlines with support. Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)  Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management.  Maintain effective relationships with study participants and other care Access Research personnel. The Expertise Required Ability to understand and follow institutional SOPs.  Excellent working knowledge of medical and research terminology  Excellent working knowledge of federal regulations, good clinical practices (GCP)  Executes tasks with supervision; requires frequent review and guidance for visits, consent support, and complex procedures. Ability to communicate and work effectively with a diverse team of professionals.  Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail  Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.  Critical thinker and problem solver  Friendly, outgoing personality; maintain a positive attitude under pressure.  High level of self-motivation and energy  Excellent professional writing and communication skills  Communicates clearly with guidance; asks questions; responds timely. Ability to work independently in a fast-paced environment with minimal supervision.  Certifications/Licenses, Education, and Experience: Bachelor’s Degree preferred, or equivalent combination of education, training, and experience. A minimum of 1-year prior Clinical Research Coordinator experience required Recent phlebotomy experience required Licenses: Louisiana based roles require National phlebotomy certification by an organization approved by the Louisiana State Board of Medical Examiners  How We Work Together Location: Position requires onsite work 5 days per week Travel: This role requires up to 10% travel within 100 miles of site. Length of travel will depend upon study requirements, staff needs, and company initiatives. Physical demands associated with this position Include: Walking, Standing, Sitting, Lifting (Up to and Overhead 25 lbs), and Driving - 20% each The expected salary range for this role is $55,000 - $85,000 USD per year for full time team members. Benefits & Perks (US Full Time Employees) Paid Time Off (PTO) and Company Paid Holidays 100% Employer paid medical, dental, and vision insurance plan options Health Savings Account and Flexible Spending Accounts Bi-weekly HSA employer contribution Company paid Short-Term Disability and Long-Term Disability 401(k) Retirement Plan, with Company Match 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 Research Coordinator at Care Access. Skills: Good Clinical Practices, Protocol compliance, Patient monitoring. Screen study subjects. 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Now get paid like it. Wellthy connects reliable caregivers with families who need last-minute childcare — school closures, holidays, unexpected work trips. You tell us your preferences (schedule, age of kids), we handle the rest. What's in it for you: 100% Schedule Control: Work twice a week or twice a month. As an independent care provider, you only accept the gigs that fit around your personal life, other opportunities, or commitments. Choose Your Track: Only want to work with toddlers, love babies? Great. Prefer hanging with older kids? Done. You only take opportunities you are comfortable with. Hassle-Free Pay: No awkward money conversations or waiting on Venmo. Get paid competitively and directly to your bank account. Earnings range from $15.00-$30.00 per hour, depending on location, experience, and family needs What You’ll Do (Choose Your Preferred Opportunity): Child Care: Keep kids engaged, safe, and off their screens with fun activities. Assist with basic routines (meals, naps, homework help). What we need from you: Experience: Some demonstrable experience in childcare (babysitting, siblings, nannying, daycare or volunteering counts!). Reliability: You show up on time and communicate clearly. Trust & Safety: To ensure the highest quality of care for our clients, all independent care providers must complete our comprehensive Trust & Safety onboarding process and meet all local, state, and enterprise childcare compliance standards. (CPR/First Aid certification is a plus!) Empathy: You genuinely care about helping families and hanging with kids. Ready to get paid for making a difference? Apply today to join the care network that fits your busy life. For those who require reasonable accommodations, please let us know on your application or email us at backupcare@wellthy.com. Wellthy provides equal platform access to all independent care providers, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristic. For questions on our Applicant Privacy Policy", "summaryDescription" : "Babysitting Opportunities at Wellthy Care Network. Skills: Child Care. Keep kids engaged. 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Now get paid like it. Wellthy connects reliable caregivers with families who need last-minute childcare — school closures, holidays, unexpected work trips. You tell us your preferences (schedule, age of kids), we handle the rest. What's in it for you: 100% Schedule Control: Work twice a week or twice a month. As an independent care provider, you only accept the gigs that fit around your personal life, other opportunities, or commitments. Choose Your Track: Only want to work with toddlers, love babies? Great. Prefer hanging with older kids? Done. You only take opportunities you are comfortable with. Hassle-Free Pay: No awkward money conversations or waiting on Venmo. Get paid competitively and directly to your bank account. Earnings range from $15.00-$30.00 per hour, depending on location, experience, and family needs What You’ll Do (Choose Your Preferred Opportunity): Child Care: Keep kids engaged, safe, and off their screens with fun activities. Assist with basic routines (meals, naps, homework help). What we need from you: Experience: Some demonstrable experience in childcare (babysitting, siblings, nannying, daycare or volunteering counts!). Reliability: You show up on time and communicate clearly. Trust & Safety: To ensure the highest quality of care for our clients, all independent care providers must complete our comprehensive Trust & Safety onboarding process and meet all local, state, and enterprise childcare compliance standards. (CPR/First Aid certification is a plus!) Empathy: You genuinely care about helping families and hanging with kids. Ready to get paid for making a difference? Apply today to join the care network that fits your busy life. For those who require reasonable accommodations, please let us know on your application or email us at backupcare@wellthy.com. Wellthy provides equal platform access to all independent care providers, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristic. For questions on our Applicant Privacy Policy", "summaryDescription" : "Babysitting Opportunities at Wellthy Care Network. Skills: Child Care. Keep kids engaged. Keep kids safe", "postedDate" : "2026-06-14T21:01:29.700", "createdAt" : "2026-06-14T21:01:29.700", "lastUpdated" : "2026-06-16T02:56:32.352", "ingestTimestamp" : "2026-06-14T21:01:29.700", "mongoId" : "6a2ca57c74d8ee00a09b6c19", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 31200, "salaryAnnualMax" : 62400, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Child Care" ], "skillCount" : 1, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.85 }, { "id" : "6a2c5dce74d8ee00a08deb2f", "title" : "Remote Clinical Research Coordinator", "company" : "UniTriTeam", "industry" : "Clinical Research", "salary" : { "min" : 1.1E7, "max" : 1.7E7, "currency" : "ARS", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Research Coordinator in Argentina, adjusted for remote work within U.S. time zones and the healthcare industry." }, "location" : "Mexico, Mexico ", "locations" : [ "Mexico", "Mexico" ], "certifications" : [ "ACRP", "SoCRA" ], "timestamp" : "2026-06-14T22:21:48.796", "fingerprint" : "6ed378710261f1fea69d776b4fffab3b25b0d25100ffdb2b4810aee91b3cfca2", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/utt/jobs/4246961009", "externalId" : "4246961009", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Argentina", "continent" : "sa", "workMode" : "remote" }, { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "Argentina; United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "technicalSkills" : "Microsoft Office Suite", "professionalSkills" : [ "Clinical trial operations", "Regulatory guidelines", "Patient recruitment", "Data entry", "Document management", "IRB submissions", "Sponsor monitoring visits", "CRO monitoring visits", "Site teams", "Study startup", "Study closeout", "Essential documents" ], "hardSkillsList" : [ "Inclusion/exclusion understanding", "Qualifying patients", "Query resolution", "Regulatory document management", "IRB submissions", "Sponsor monitoring", "CRO monitoring", "Audit preparation", "Inspection preparation", "Essential document collection", "Essential document verification" ], "softSkillsList" : [ "Attention to detail" ], "hardSkills" : [ { "name" : "Inclusion/exclusion understanding", "level" : "intermediate" }, { "name" : "Qualifying patients", "level" : "intermediate" }, { "name" : "Query resolution", "level" : "intermediate" }, { "name" : "Regulatory document management", "level" : "intermediate" }, { "name" : "IRB submissions", "level" : "intermediate" }, { "name" : "Sponsor monitoring", "level" : "intermediate" }, { "name" : "CRO monitoring", "level" : "intermediate" }, { "name" : "Audit preparation", "level" : "intermediate" }, { "name" : "Inspection preparation", "level" : "intermediate" }, { "name" : "Essential document collection", "level" : "intermediate" }, { "name" : "Essential document verification", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Attention to detail" } ], "majorSkills" : "Clinical research coordination, Remote patient visits, Clinical trial support", "majorSkillsList" : [ "Clinical research coordination", "Remote patient visits", "Clinical trial support" ], "coreResponsibilities" : "Coordinate day-to-day clinical trial operations, Ensure compliance with study protocols, Ensure compliance with regulatory guidelines, Support remote patient visits, Facilitate remote patient visits, Maintain accurate data entry in EDC, Maintain timely data entry in EDC, Manage query resolution, Assist with regulatory document management, Assist with remote IRB submissions, Assist with remote IRB updates, Prepare for remote sponsor monitoring visits, Prepare for remote CRO monitoring visits, Prepare for remote audits, Prepare for remote inspections, Serve as a virtual liaison with sponsors, Serve as a virtual liaison with CROs, Serve as a virtual liaison with internal site, Support study startup tasks, Support study closeout tasks, Support remote collection of essential documents, Support remote verification of essential documents, Monitor visit schedules, Ensure all subject documentation is complete, Ensure all subject documentation is up to date", "teamCollaboration" : "Virtual liaison with sponsors; Virtual liaison with CROs; Virtual liaison with internal site teams; Global team collaboration", "domainKnowledge" : "Clinical research; GCP; ICH; FDA regulatory requirements", "domainList" : [ "clinical-research", "gcp", "ich", "fda-regulatory-requirements" ], "domainSpecificKnowledge" : [ "Clinical research", "GCP", "ICH", "FDA regulatory requirements" ], "toolProficiency" : [ "CTMS platforms", "CRIO", "Clinical Conductor", "EDC", "Zoom", "Teams" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Documentation accuracy; Regulatory document management; Essential documents", "continuousLearning" : "Professional development; Growth opportunities", "qualificationsBasic" : "2+ years of experience in clinical research coordination or clinical operations, understanding of GCP, ICH, and FDA regulatory requirements, Fluent in English – both verbal and written communication required, Comfortable working independently in a fully remote setting across multiple time zones, Highly organized with attention to detail and documentation accuracy", "qualificationsPreferred" : "Associate or Bachelor’s degree in health sciences or related field, Clinical research certification (e.g., ACRP, SoCRA), Prior experience supporting multi-site trials remotely, Bilingual proficiency is a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Remote Clinical Research Coordinator (Remote – PST/CST/EST Hours) LOCATION: India Job Description: Remote Clinical Research Coordinator Location: Remote – U. S. Time Zones Preferred Client: This position is in partnership with a client of UniTriTeam, a leader in clinical research support and global staffing. About the Role: UniTriTeam is seeking a Remote Clinical Research Coordinator (CRC) to support one of our clinical research site clients. This position is fully remote and does not involve in-person patient interaction, but will require coordination and facilitation of remote patient visits, as well as all behind-the-scenes clinical trial support. The ideal candidate has strong communication skills, is detail-oriented, and has experience using CTMS platforms such as CRIO or Clinical Conductor. Key Responsibilities: Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines. Support and facilitate remote patient visits, including scheduling, documentation, and follow-up. Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone. Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution. Assist with regulatory document management and remote IRB submissions and updates. Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections. Serve as a virtual liaison with sponsors, CROs, and internal site teams. Support study startup and closeout tasks, including remote collection and verification of essential documents. Monitor visit schedules and ensure all subject documentation is complete and up to date. Required Qualifications: 2+ years of experience in clinical research coordination or clinical operations. Strong understanding of GCP, ICH, and FDA regulatory requirements. Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred. Fluent in English – both verbal and written communication required. Comfortable working independently in a fully remote setting across multiple time zones. Highly organized with strong attention to detail and documentation accuracy. Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.). Preferred Qualifications: Associate or Bachelor’s degree in health sciences or related field. Clinical research certification (e.g., ACRP, SoCRA). Prior experience supporting multi-site trials remotely. Bilingual proficiency is a plus. Work Schedule: Full-time (Remote), U. S. time zones (EST to PST) Perks of Working with UniTriTeam: Work with a mission-driven organization transforming the clinical research industry. Fully remote work environment with global team collaboration. Exposure to innovative research sites and a wide variety of protocols. Professional development and growth opportunities. Supportive and inclusive team culture. Why Join Us? UniTriTeam is a global leader in providing operational, administrative, and technology support to clinical research sites. We take pride in our mission to help advance medicine and make a real impact in healthcare. By joining our team, you’ll benefit from: A collaborative and supportive work environment Opportunities for professional growth and advancement A chance to be part of meaningful research initiatives that change lives", "summaryDescription" : "Remote Clinical Research Coordinator at UniTriTeam. Skills: Clinical research coordination, Remote patient visits, Clinical trial support. Coordinate day-to-day clinical trial operations. Ensure compliance with study protocols", "postedDate" : "2026-06-12T21:38:47.870", "createdAt" : "2026-06-12T21:38:47.870", "lastUpdated" : "2026-06-14T22:21:48.796", "ingestTimestamp" : "2026-06-12T21:38:47.870", "mongoId" : "6a2c5dce74d8ee00a08deb2f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Inclusion/exclusion understanding", "Qualifying patients", "Query resolution", "Regulatory document management", "IRB submissions", "Sponsor monitoring", "CRO monitoring", "Audit preparation", "Inspection preparation", "Essential document collection", "Essential document verification", "Attention to detail", "Clinical research coordination", "Remote patient visits", "Clinical trial support", "Clinical trial operations", "Regulatory guidelines", "Patient recruitment", "Data entry", "Document management", "Sponsor monitoring visits", "CRO monitoring visits", "Site teams", "Study startup", "Study closeout", "Essential documents", "Clinical research", "GCP", "ICH", "FDA regulatory requirements", "ACRP", "SoCRA", "CTMS platforms", "CRIO", "Clinical Conductor", "EDC", "Zoom", "Teams" ], "skillCount" : 38, "jobCategory" : "other", "jobSubcategory" : "clinical-research", "dataQualityScore" : 1.0, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Clinical Research" }, { "id" : "6a2c5dce74d8ee00a08deb28", "title" : "Clinical Research Operations Associate", "company" : "UniTriTeam", "industry" : "Clinical Research", "salary" : { "min" : 95000.0, "max" : 135000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Clinical Research Operations Associate in the US Biotech industry, adjusted for remote work and company size." }, "location" : "Mexico, Mexico ", "locations" : [ "Mexico", "Mexico" ], "timestamp" : "2026-06-14T22:53:46.100", "fingerprint" : "582d0fbf4c9f00ed43310dfb0cc79ad2ef49f7e7f98c567582c37c5160c81c9f", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/utt/jobs/4115932009", "externalId" : "4115932009", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Microsoft Office Suite", "professionalSkills" : [ "Clinical research operations", "Trial coordination", "Patient recruitment", "Contracting", "e-Source design", "Study execution", "Site-level processes", "Clinical trial operations", "Project management" ], "hardSkillsList" : [ "Clinical research", "Project management" ], "softSkillsList" : [ "Adaptability" ], "hardSkills" : [ { "name" : "Clinical research", "level" : "intermediate" }, { "name" : "Project management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Adaptability" } ], "majorSkills" : "Clinical research operations, Project management, Operational execution", "majorSkillsList" : [ "Clinical research operations", "Project management", "Operational execution" ], "coreResponsibilities" : "Provide day-to-day operational support to VP of Operations, Relieve workload for VP of Operations, Manage operational projects, Execute operational projects, Ensure project timelines are met, Ensure project deliverables are met, Support patient recruitment, Support contracting, Support study execution, Support development of e-source templates, Support design of e-source workflows, Provide oversight on contracts, Provide input on contracts, Provide oversight on budgets, Provide input on budgets, Provide oversight on site-level processes, Provide input on site-level processes, Serve as subject matter expert across clinical research, Anticipate needs, Proactively resolve issues, Keep projects moving forward, Develop documentation, Develop SOPs, Develop best practices, Support continuous improvement initiatives", "teamCollaboration" : "Cross-functional teams", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Clinical research; Clinical trial operations; Coordinator-level responsibilities", "domainList" : [ "clinical-research", "clinical-trial-operations", "coordinator-level-responsibilities" ], "domainSpecificKnowledge" : [ "Clinical research", "Clinical trial operations", "Coordinator-level responsibilities" ], "toolProficiency" : [ "Microsoft Office Suite", "Project management tools" ], "documentationSkills" : "Develop documentation", "continuousLearning" : "Comprehensive onboarding; Training program", "problemSolvingSkills" : "Problem-solving skills", "qualificationsBasic" : "5 years clinical research experience, Direct knowledge of clinical research coordinator duties, Direct knowledge of patient recruitment, Direct knowledge of contracting, Experience with e-source design and implementation, Understanding of clinical trial operations from startup through closeout, Ability to manage projects independently, Ability to deliver results without extensive supervision, Proficiency in Microsoft Office Suite, Proficiency in project management tools, Central Time Zone alignment", "qualificationsPreferred" : "CRIO experience preferred, Clinical Conductor experience preferred, RealTime experience preferred", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Job Description Title: Clinical Research Operations Associate (Right Hand to VP of Operations) Location: Remote – Central Time Zone alignment required Hours: Full-time Position Summary UniTriTeam is hiring a Clinical Research Operations Associate to serve as the right hand to the VP of Operations at our client, a fast-growing clinical research organization. This role is designed for a seasoned professional with in-depth clinical research experience who can independently manage projects, provide operational support, and reduce workload for the VP of Operations. The ideal candidate has performed multiple roles within clinical research operations — from coordinating trials, to patient recruitment, to contracting, to e-source design — and can bring this knowledge to drive operational excellence. This position requires a proactive, detail-oriented, and adaptable individual who thrives in a fast-paced startup environment and can take ownership with minimal oversight. Key Responsibilities Act as the right hand to the VP of Operations, providing day-to-day operational support and workload relief. Manage and execute operational projects, ensuring timelines and deliverables are consistently met. Leverage expertise in clinical research operations to support patient recruitment, contracting, and study execution. Support the development and design of e-source templates and workflows. Provide oversight and input on contracts, budgets, and site-level processes. Serve as a subject matter expert across the clinical research lifecycle, including coordinator-level responsibilities. Anticipate needs and proactively resolve issues to keep projects moving forward. Develop documentation, SOPs, and best practices to support continuous improvement initiatives. Qualifications Minimum 5 years of clinical research experience, with direct knowledge of clinical research coordinator duties, patient recruitment, and contracting. Experience with e-source design and implementation (CRIO, Clinical Conductor, RealTime strongly preferred). Strong understanding of clinical trial operations from startup through closeout. Demonstrated ability to manage projects independently and deliver results without extensive supervision. Excellent organizational, communication, and problem-solving skills. Adaptability to thrive in a fast-paced startup environment. Ability to work full-time, remote, aligned to Central Time Zone. Proficiency in Microsoft Office Suite and project management tools. Core Competencies Clinical Research Expertise – deep understanding of operations across the trial lifecycle. Operational Execution – ability to turn high-level direction into actionable results. Proactivity – anticipating needs and removing obstacles for leadership. Project Management – ensuring timelines, tasks, and deliverables stay on track. Adaptability – thriving in dynamic environments with shifting priorities. What Sets UniTriTeam Apart At UniTriTeam, we believe in creating win-win-win solutions for our clients, our team members, and the clinical research industry. Every UniTriTeam professional goes through a comprehensive onboarding and training program that includes communication, project management, and AI tool integration — at no additional cost to the client. Our model ensures that team members are fully prepared to integrate seamlessly into client organizations and deliver immediate value. With over 45 years of combined leadership experience in clinical research site operations, UniTriTeam provides unmatched support, scalability, and flexibility to help research sites thrive. Employment Details This position will be employed by UniTriTeam and fully dedicated to supporting Elevate Clinical Research.", "summaryDescription" : "Clinical Research Operations Associate at UniTriTeam. Skills: Clinical research operations, Project management, Operational execution. Provide day-to-day operational support to VP of Operations. Relieve workload for VP of Operations", "postedDate" : "2026-06-12T21:38:39.455", "createdAt" : "2026-06-12T21:38:39.455", "lastUpdated" : "2026-06-14T22:53:46.100", "ingestTimestamp" : "2026-06-12T21:38:39.455", "mongoId" : "6a2c5dce74d8ee00a08deb28", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 135000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Clinical research", "Project management", "Adaptability", "Clinical research operations", "Operational execution", "Trial coordination", "Patient recruitment", "Contracting", "e-Source design", "Study execution", "Site-level processes", "Clinical trial operations", "Coordinator-level responsibilities", "Microsoft Office Suite", "Project management tools" ], "skillCount" : 15, "jobCategory" : "other", "jobSubcategory" : "clinical-research", "dataQualityScore" : 1.0, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Clinical Research" }, { "id" : "69dde45b2beec4dd3d9a3f40", "title" : "Clinical Research Nurse-BSN", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Clinical Research Nurse in Duarte, California, adjusted for the healthcare industry and a large company size." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Population Sciences", "Onsite, Days, Days" ], "timestamp" : "2026-06-16T02:38:17.364", "fingerprint" : "874f671c9093998149a0f1c82d32574d425472676e733577740aa18699518e52", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=232205", "externalId" : "232205", "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" : "Bachelor's", "remoteFriendly" : false, "rawDescription" : "Clinical Research Nurse 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. Work collaboratively with the principal investigator, Clinical Research Associates (CRA), and other Clinical Research Nurses (CRNs) on the conduct of multiple federally-funded trials to test supportive interventions to improve quality of life and quality of care for patients with cancer and their family caregivers. Specifically, the CRN will be responsible for the delivery of telehealth/remote telemonitoring-driven interventions (assessments, telehealth calls, triage management, education) to improve symptom management, quality of life, and reduce caregiving burden for patients with cancer and their family caregivers. The CRN role will also include coordination/communication with patients/family caregivers, oncology team and clinicians (physicians, APPs, supportive care medicine etc). The position will be on a highly collaborative team, with a great support structure, working hard to meet milestones and targets, but taking the time to celebrate victories and supporting each other throughout the work. As a successful candidate, you will: Collaborate with the investigator to ascertain study patient eligibility for clinical trial, including documentation of criteria specified in the clinical trial. Assess, identify and prioritize clinical information to physician, NP, PA and other clinicians for patients who are being evaluated or who are enrolled in to IRB clinical trials. Assess and document signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB protocol assuring that the documentation is complete and accurate in order to avoid protocol deviations. Manage patient/family phone calls – collaborating with MD, NP and/or PA as needed to obtain orders for the management of the patient. Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations. Your qualifications should include: BSN 2 or more years of experience in oncology. clinical research, research, ICU, other intensive care setting, pediatrics, case management or nurse navigation. Human subjects protection training (can be completed after hire) Required Certification/Licensure: Current California RN License American Heart Association BLS Certification City of Hope is an equal opportunity employer. United States-California-Duarte", "summaryDescription" : "Clinical Research Nurse-BSN at City of Hope", "createdAt" : "2026-06-14T20:42:36.723", "lastUpdated" : "2026-06-16T02:38:17.364", "ingestTimestamp" : "2026-06-14T20:42:36.723", "mongoId" : "69dde45b2beec4dd3d9a3f40", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 105000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Junior", "dataQualityScore" : 0.5555556, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a19719958b93c861e516da4", "title" : "Clinical Research Program Navigator", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 75000.0, "max" : 115000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline data for a Mid-level Clinical Research Program Navigator in the Healthcare industry in the United States, adjusted for remote work and company size." }, "location" : "US-Nationwide-USA-Remote", "locations" : [ "US-Nationwide-USA-Remote", "Clinical Research", "Remote, Days, Days" ], "timestamp" : "2026-06-16T00:56:57.864", "fingerprint" : "a93f2d1b62d40cbcee4420b445f5b134e4fb277893f3b48d4fe4a4b7ea3835cd", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=235544", "externalId" : "235544", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "minimumEducation" : "Bachelor's Degree", "coreResponsibilities" : "Manage customer relationships, Drive customer retention, Ensure customer satisfaction, Facilitate customer value realization", "remoteFriendly" : true, "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. Join our Clinical Research team and play a vital role in improving the patient and family experience throughout the clinical trial journey. As a Clinical Research Program Navigator, you will guide patients with cancer and their families by connecting them to resources, removing barriers to care, and ensuring a smooth, supportive experience from start to finish. Collaborate closely with Research teams, care providers and support services to enhance processes, improve outcomes, and ensure patients receive the highest level of coordinated care. As a successful candidate, you will: Serve as a primary point of contact for clinical trial patients and families, providing guidance, education, and ongoing support Introduce patients to available programs, services and resources. Help navigate the care continuum Assess patient and family needs, identify potential barriers, coordinate solutions to support treatment adherence Act as a liaison between research, clinical teams, and support departments to improve the overall care experience Provide proactive follow-up, including post-treatment check-ins and appointment reminders for at-risk patients. Assist with scheduling coordination and ensure efficient, patient-centered care planning Document patient interactions and maintain accurate records Availability to commute 10% of the time to meet with patients Your qualifications should include: Bachelor's Degree 5 years or more of experience working in a hospital/healthcare setting and interacting collaboratively with medical teams Strong customer service skills Demonstrate skills in written and verbal communication including good phone etiquette Good problem solving skills Display sensitivity to patient care, privacy and cultural needs. Preferred education, experience and skills: Master's Degree in Health or Health-related field Knowledge of oncology healthcare and psychosocial needs Previous grant and/or clinical trial experience 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 . US-Nationwide-USA-Remote", "summaryDescription" : "Clinical Research Program Navigator at City of Hope. Manage customer relationships. Drive customer retention", "createdAt" : "2026-06-14T19:42:55.315", "lastUpdated" : "2026-06-16T00:56:57.864", "ingestTimestamp" : "2026-06-14T19:42:55.315", "mongoId" : "6a19719958b93c861e516da4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 115000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "sales", "jobSubcategory" : "customer_success", "seniorityLevel" : "Mid", "dataQualityScore" : 0.5555556, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ca57c74d8ee00a09b6c58", "title" : "Babysitting Opportunities", "company" : "Wellthy Care Network", "industry" : "Hospitality", "salary" : { "min" : 15.0, "max" : 30.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Backup Care", "locations" : [ "Backup Care" ], "timestamp" : "2026-06-15T05:22:08.579", "fingerprint" : "ca66d44edef97059cdd28008aa53a0f4666c90a2de226a037d2f9ecce3281b8c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/wellthy-care-network/jobs/7771756003", "externalId" : "7771756003", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Mountain View", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.3893889,-122.0832101" } ], "locationText" : "Mountain View, California, United States", "majorSkills" : "Child Care", "majorSkillsList" : [ "Child Care" ], "coreResponsibilities" : "Keep kids engaged, Keep kids safe, Assist with basic routines", "specialRequirements" : "Trust & Safety onboarding", "qualificationsBasic" : "Demonstrable childcare experience", "qualificationsPreferred" : "CPR/First Aid certification", "workSiteFlexibility" : "Flexible", "rawDescription" : "Babysitting Opportunities - Mountain View, CA You're already the person families trust with their kids. Now get paid like it. Wellthy connects reliable caregivers with families who need last-minute childcare — school closures, holidays, unexpected work trips. You tell us your preferences (schedule, age of kids), we handle the rest. What's in it for you: 100% Schedule Control: Work twice a week or twice a month. As an independent care provider, you only accept the gigs that fit around your personal life, other opportunities, or commitments. Choose Your Track: Only want to work with toddlers, love babies? Great. Prefer hanging with older kids? Done. You only take opportunities you are comfortable with. Hassle-Free Pay: No awkward money conversations or waiting on Venmo. Get paid competitively and directly to your bank account. Earnings range from $15.00-$30.00 per hour, depending on location, experience, and family needs What You’ll Do (Choose Your Preferred Opportunity): Child Care: Keep kids engaged, safe, and off their screens with fun activities. Assist with basic routines (meals, naps, homework help). What we need from you: Experience: Some demonstrable experience in childcare (babysitting, siblings, nannying, daycare or volunteering counts!). Reliability: You show up on time and communicate clearly. Trust & Safety: To ensure the highest quality of care for our clients, all independent care providers must complete our comprehensive Trust & Safety onboarding process and meet all local, state, and enterprise childcare compliance standards. (CPR/First Aid certification is a plus!) Empathy: You genuinely care about helping families and hanging with kids. Ready to get paid for making a difference? Apply today to join the care network that fits your busy life. For those who require reasonable accommodations, please let us know on your application or email us at backupcare@wellthy.com. Wellthy provides equal platform access to all independent care providers, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristic. For questions on our Applicant Privacy Policy", "summaryDescription" : "Babysitting Opportunities at Wellthy Care Network. Skills: Child Care. Keep kids engaged. Keep kids safe", "postedDate" : "2026-06-14T04:44:56.140", "createdAt" : "2026-06-14T04:44:56.140", "lastUpdated" : "2026-06-15T05:22:08.579", "ingestTimestamp" : "2026-06-14T04:44:56.140", "mongoId" : "6a2ca57c74d8ee00a09b6c58", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 31200, "salaryAnnualMax" : 62400, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Child Care" ], "skillCount" : 1, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.85 }, { "id" : "6a2a765674d8ee00a065bdd0", "title" : "Clinical Research Associate I/ Clinical Research Associate II", "company" : "Precision for Medicine", "industry" : "Life sciences", "salary" : { "min" : 42000.0, "max" : 58000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Junior Clinical Research Associate I/II in the Biotech industry in France, adjusted for seniority and remote work." }, "location" : "Remote (France)", "locations" : [ "Remote (France)" ], "timestamp" : "2026-06-14T23:16:41.131", "fingerprint" : "176e83e4816f63e3f46be34c53424c04c0dcde5aa6bb20f00c313c1084bc0a5c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/pfm/jobs/5807098004", "externalId" : "5807098004", "industryFunction" : { }, "structuredLocations" : [ { "country" : "France", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "France", "minimumEducation" : "Life science degree", "experienceMinYears" : 1, "professionalSkills" : [ "Site management", "Clinical research" ], "hardSkillsList" : [ "Protocol execution", "Regulatory submissions", "Study monitoring" ], "softSkillsList" : [ "Calm", "Thoughtful", "Responsive", "Prepared", "Creative", "Conflict resolution" ], "hardSkills" : [ { "name" : "Protocol execution", "level" : "intermediate" }, { "name" : "Regulatory submissions", "level" : "intermediate" }, { "name" : "Study monitoring", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Calm" }, { "name" : "Thoughtful" }, { "name" : "Responsive" }, { "name" : "Prepared" }, { "name" : "Creative" }, { "name" : "Conflict resolution" } ], "majorSkills" : "Clinical trial execution, Scientific knowledge, Data sciences", "majorSkillsList" : [ "Clinical trial execution", "Scientific knowledge", "Data sciences" ], "coreResponsibilities" : "Monitor study progress at investigative sites, Ensure studies are conducted per protocol, Coordinate study setup activities, Prepare regulatory submissions, Conduct pre-study visits, Conduct initiation visits", "domainKnowledge" : "Oncology; Rare Disease; ICH-GCP; Applicable regulations", "domainList" : [ "oncology", "rare-disease", "ich-gcp", "applicable-regulations" ], "domainSpecificKnowledge" : [ "Oncology", "Rare Disease", "ICH-GCP", "Applicable regulations" ], "communicationSkills" : "Organizational skills", "problemSolvingSkills" : "Identify study risks; Propose mitigation solutions; Overcome difficulties", "specialRequirements" : "Domestic travel up to 50-60%, Overnight stays", "outcomesObjectives" : "Quality and outcomes of work", "qualificationsBasic" : "Life science degree or equivalent experience, 1+ year CRA experience, Site management experience, Oncology studies experience, Availability for domestic travel, Fluency in English, Fluency in local language", "qualificationsPreferred" : "Study start up experience", "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 passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management. We are now recruiting Clinical Research Associate I/ Clinical Research Associate II to join our team in France. This is a remote based position with travel to sites for monitoring visits. We are looking for candidates based in Paris or Paris area. About you: You are calm, thoughtful, and responsive when things don’t go as planned. You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game. You find quick and creative ways of overcoming difficulties. You have an impeccable eye for detail. You identify potential study risks and propose solutions on how to mitigate them. You take responsibility in the quality and outcomes of your work. You are adept at handling conflict by using tried and true resolution strategies. How we will keep you busy and support your growth: You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.). Qualifications: Minimum Required: Life science degree and / or equivalent experience 1 year or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management or equivalent experience in clinical research. Experience managing oncology studies Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions) Other Required: Excellent communication and organizational skills are essential. A team player. Evidence of a client focused approach Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions) Fluency in English and for non-English speaking countries the local language of country where position based Preferred: Study start up activities experience. Please apply in English. #LI-EK1 #LI-Remote 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 Research Associate I/ Clinical Research Associate II at Precision for Medicine. Skills: Clinical trial execution, Scientific knowledge, Data sciences. Monitor study progress at investigative sites. Ensure studies are conducted per protocol", "postedDate" : "2026-06-12T00:38:24.395", "createdAt" : "2026-06-12T00:38:24.395", "lastUpdated" : "2026-06-14T23:16:41.131", "ingestTimestamp" : "2026-06-12T00:38:24.395", "mongoId" : "6a2a765674d8ee00a065bdd0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Protocol execution", "Regulatory submissions", "Study monitoring", "Calm", "Thoughtful", "Responsive", "Prepared", "Creative", "Conflict resolution", "Clinical trial execution", "Scientific knowledge", "Data sciences", "Site management", "Clinical research", "Oncology", "Rare Disease", "ICH-GCP", "Applicable regulations" ], "skillCount" : 18, "jobCategory" : "other", "jobSubcategory" : "clinical-solutions", "dataQualityScore" : 0.7777778, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Life sciences" }, { "id" : "6a2c5dce74d8ee00a08deb2e", "title" : "Remote Clinical Research Coordinator", "company" : "UniTriTeam", "industry" : "Clinical Research", "salary" : { "min" : 1.1E7, "max" : 1.7E7, "currency" : "ARS", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Research Coordinator in Argentina, adjusted for remote work within U.S. time zones and the healthcare industry." }, "location" : "Mexico, Mexico ", "locations" : [ "Mexico", "Mexico" ], "certifications" : [ "ACRP", "SoCRA" ], "timestamp" : "2026-06-14T22:35:16.959", "fingerprint" : "fc927bec9541765ee505c4e7714329008bf993ebbe13f076ecd073eb84905db6", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/utt/jobs/4246956009", "externalId" : "4246956009", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Argentina", "continent" : "sa", "workMode" : "remote" }, { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "Argentina; United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "technicalSkills" : "Microsoft Office Suite", "professionalSkills" : [ "Clinical trial operations", "Patient recruitment", "Regulatory document management", "Study startup", "Study closeout" ], "hardSkillsList" : [ "Data entry", "Query resolution" ], "hardSkills" : [ { "name" : "Data entry", "level" : "intermediate" }, { "name" : "Query resolution", "level" : "intermediate" } ], "majorSkills" : "Clinical research coordination, Remote patient visits", "majorSkillsList" : [ "Clinical research coordination", "Remote patient visits" ], "coreResponsibilities" : "Coordinate day-to-day clinical trial operations in a remote, Ensure compliance with study protocols and regulatory guidelines, Support and facilitate remote patient visits, Maintain accurate and timely data entry in EDC, Manage query resolution, Assist with regulatory document management, Assist with remote IRB submissions and updates, Prepare for and participate in remote sponsor/CRO monitoring, Prepare for and participate in remote audits and, Serve as a virtual liaison with sponsors, CROs,, Support study startup tasks, Support study closeout tasks, Collect and verify essential documents remotely, Monitor visit schedules, Ensure all subject documentation is complete and up", "teamCollaboration" : "Virtual liaison with sponsors; Virtual liaison with CROs; Virtual liaison with internal site teams; Global team collaboration", "domainKnowledge" : "GCP; ICH; FDA regulatory requirements; Clinical research protocols", "domainList" : [ "gcp", "ich", "fda-regulatory-requirements", "clinical-research-protocols" ], "domainSpecificKnowledge" : [ "GCP", "ICH", "FDA regulatory requirements", "Clinical research protocols" ], "toolProficiency" : [ "CTMS platforms", "CRIO", "Clinical Conductor", "EDC", "Zoom", "Teams" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Documentation accuracy", "continuousLearning" : "Professional development; Growth opportunities", "qualificationsBasic" : "2+ years of experience in clinical research coordination or clinical operations, understanding of GCP, ICH, and FDA regulatory requirements, Fluent in English – both verbal and written communication required, Comfortable working independently in a fully remote setting across multiple time zones, Highly organized with attention to detail and documentation accuracy", "qualificationsPreferred" : "Associate or Bachelor’s degree in health sciences or related field, Clinical research certification (e.g., ACRP, SoCRA), Prior experience supporting multi-site trials remotely, Bilingual proficiency is a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Remote Clinical Research Coordinator (Remote – PST/CST/EST Hours) LOCATION: Brazil Job Description: Remote Clinical Research Coordinator Location: Remote – U. S. Time Zones Preferred Client: This position is in partnership with a client of UniTriTeam, a leader in clinical research support and global staffing. About the Role: UniTriTeam is seeking a Remote Clinical Research Coordinator (CRC) to support one of our clinical research site clients. This position is fully remote and does not involve in-person patient interaction, but will require coordination and facilitation of remote patient visits, as well as all behind-the-scenes clinical trial support. The ideal candidate has strong communication skills, is detail-oriented, and has experience using CTMS platforms such as CRIO or Clinical Conductor. Key Responsibilities: Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines. Support and facilitate remote patient visits, including scheduling, documentation, and follow-up. Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone. Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution. Assist with regulatory document management and remote IRB submissions and updates. Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections. Serve as a virtual liaison with sponsors, CROs, and internal site teams. Support study startup and closeout tasks, including remote collection and verification of essential documents. Monitor visit schedules and ensure all subject documentation is complete and up to date. Required Qualifications: 2+ years of experience in clinical research coordination or clinical operations. Strong understanding of GCP, ICH, and FDA regulatory requirements. Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred. Fluent in English – both verbal and written communication required. Comfortable working independently in a fully remote setting across multiple time zones. Highly organized with strong attention to detail and documentation accuracy. Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.). Preferred Qualifications: Associate or Bachelor’s degree in health sciences or related field. Clinical research certification (e.g., ACRP, SoCRA). Prior experience supporting multi-site trials remotely. Bilingual proficiency is a plus. Work Schedule: Full-time (Remote), U. S. time zones (EST to PST) Perks of Working with UniTriTeam: Work with a mission-driven organization transforming the clinical research industry. Fully remote work environment with global team collaboration. Exposure to innovative research sites and a wide variety of protocols. Professional development and growth opportunities. Supportive and inclusive team culture. Why Join Us? UniTriTeam is a global leader in providing operational, administrative, and technology support to clinical research sites. We take pride in our mission to help advance medicine and make a real impact in healthcare. By joining our team, you’ll benefit from: A collaborative and supportive work environment Opportunities for professional growth and advancement A chance to be part of meaningful research initiatives that change lives", "summaryDescription" : "Remote Clinical Research Coordinator at UniTriTeam. Skills: Clinical research coordination, Remote patient visits. Coordinate day-to-day clinical trial operations in a remote. 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S. Time Zones Preferred Client: This position is in partnership with a client of UniTriTeam, a leader in clinical research support and global staffing. About the Role: UniTriTeam is seeking a Remote Clinical Research Coordinator (CRC) to support one of our clinical research site clients. This position is fully remote and does not involve in-person patient interaction, but will require coordination and facilitation of remote patient visits, as well as all behind-the-scenes clinical trial support. The ideal candidate has strong communication skills, is detail-oriented, and has experience using CTMS platforms such as CRIO or Clinical Conductor. Key Responsibilities: Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines. Support and facilitate remote patient visits, including scheduling, documentation, and follow-up. Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone. Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution. Assist with regulatory document management and remote IRB submissions and updates. Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections. Serve as a virtual liaison with sponsors, CROs, and internal site teams. Support study startup and closeout tasks, including remote collection and verification of essential documents. Monitor visit schedules and ensure all subject documentation is complete and up to date. Required Qualifications: 2+ years of experience in clinical research coordination or clinical operations. Strong understanding of GCP, ICH, and FDA regulatory requirements. Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred. Fluent in English – both verbal and written communication required. Comfortable working independently in a fully remote setting across multiple time zones. Highly organized with strong attention to detail and documentation accuracy. Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.). Preferred Qualifications: Associate or Bachelor’s degree in health sciences or related field. Clinical research certification (e.g., ACRP, SoCRA). Prior experience supporting multi-site trials remotely. Bilingual proficiency is a plus. Work Schedule: Full-time (Remote), U. S. time zones (EST to PST) Perks of Working with UniTriTeam: Work with a mission-driven organization transforming the clinical research industry. Fully remote work environment with global team collaboration. Exposure to innovative research sites and a wide variety of protocols. Professional development and growth opportunities. Supportive and inclusive team culture. Why Join Us? UniTriTeam is a global leader in providing operational, administrative, and technology support to clinical research sites. We take pride in our mission to help advance medicine and make a real impact in healthcare. By joining our team, you’ll benefit from: A collaborative and supportive work environment Opportunities for professional growth and advancement A chance to be part of meaningful research initiatives that change lives", "summaryDescription" : "Remote Clinical Research Coordinator at UniTriTeam. Skills: Clinical trial operations, Remote patient visits, Data entry. Coordinate day-to-day clinical trial operations. 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Virtual liaison with CROs; Virtual liaison with internal site teams; Global team collaboration", "domainKnowledge" : "Clinical research; GCP; ICH; FDA regulations", "domainList" : [ "clinical-research", "gcp", "ich", "fda-regulations" ], "domainSpecificKnowledge" : [ "Clinical research", "GCP", "ICH", "FDA regulations" ], "toolProficiency" : [ "CRIO", "Clinical Conductor", "EDC", "Microsoft Office Suite", "Zoom", "Teams" ], "communicationSkills" : "English verbal communication; English written communication", "documentationSkills" : "Data entry; Regulatory document management; Essential documents", "continuousLearning" : "Professional development; Growth opportunities", "specialRequirements" : "Remote – U. S. Time Zones, PST/EST/CST Timezone", "qualificationsBasic" : "2+ years clinical research coordination, 2+ years clinical operations, GCP, ICH, and FDA regulatory requirements understanding, Proficiency with CTMS platforms, Fluent in English, Comfortable working independently, Highly organized, Attention to detail, Documentation accuracy, Proficient in Microsoft Office Suite, Proficient in remote communication platforms", "qualificationsPreferred" : "Associate degree in health sciences, Bachelor's degree in health sciences, Clinical research certification, Prior experience supporting multi-site trials remotely, Bilingual proficiency", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Remote Clinical Research Coordinator (Remote – PST/CST/EST Hours) LOCATION: Mexico Job Description: Remote Clinical Research Coordinator Location: Remote – U. S. Time Zones Preferred Client: This position is in partnership with a client of UniTriTeam, a leader in clinical research support and global staffing. About the Role: UniTriTeam is seeking a Remote Clinical Research Coordinator (CRC) to support one of our clinical research site clients. This position is fully remote and does not involve in-person patient interaction, but will require coordination and facilitation of remote patient visits, as well as all behind-the-scenes clinical trial support. The ideal candidate has strong communication skills, is detail-oriented, and has experience using CTMS platforms such as CRIO or Clinical Conductor. Key Responsibilities: Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines. Support and facilitate remote patient visits, including scheduling, documentation, and follow-up. Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone. Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution. Assist with regulatory document management and remote IRB submissions and updates. Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections. Serve as a virtual liaison with sponsors, CROs, and internal site teams. Support study startup and closeout tasks, including remote collection and verification of essential documents. Monitor visit schedules and ensure all subject documentation is complete and up to date. Required Qualifications: 2+ years of experience in clinical research coordination or clinical operations. Strong understanding of GCP, ICH, and FDA regulatory requirements. Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred. Fluent in English – both verbal and written communication required. Comfortable working independently in a fully remote setting across multiple time zones. Highly organized with strong attention to detail and documentation accuracy. Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.). Preferred Qualifications: Associate or Bachelor’s degree in health sciences or related field. Clinical research certification (e.g., ACRP, SoCRA). Prior experience supporting multi-site trials remotely. Bilingual proficiency is a plus. Work Schedule: Full-time (Remote), U. S. time zones (EST to PST) Perks of Working with UniTriTeam: Work with a mission-driven organization transforming the clinical research industry. Fully remote work environment with global team collaboration. Exposure to innovative research sites and a wide variety of protocols. Professional development and growth opportunities. Supportive and inclusive team culture. Why Join Us? UniTriTeam is a global leader in providing operational, administrative, and technology support to clinical research sites. We take pride in our mission to help advance medicine and make a real impact in healthcare. By joining our team, you’ll benefit from: A collaborative and supportive work environment Opportunities for professional growth and advancement A chance to be part of meaningful research initiatives that change lives", "summaryDescription" : "Remote Clinical Research Coordinator at UniTriTeam. Skills: Clinical research coordination, Clinical operations, CTMS platforms. Coordinate day-to-day clinical trial operations. 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S. Time Zones Preferred Client: This position is in partnership with a client of UniTriTeam, a leader in clinical research support and global staffing. About the Role: UniTriTeam is seeking a Remote Clinical Research Coordinator (CRC) to support one of our clinical research site clients. This position is fully remote and does not involve in-person patient interaction, but will require coordination and facilitation of remote patient visits, as well as all behind-the-scenes clinical trial support. The ideal candidate has strong communication skills, is detail-oriented, and has experience using CTMS platforms such as CRIO or Clinical Conductor. Key Responsibilities: Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines. Support and facilitate remote patient visits, including scheduling, documentation, and follow-up. Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone. Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution. Assist with regulatory document management and remote IRB submissions and updates. Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections. Serve as a virtual liaison with sponsors, CROs, and internal site teams. Support study startup and closeout tasks, including remote collection and verification of essential documents. Monitor visit schedules and ensure all subject documentation is complete and up to date. Required Qualifications: 2+ years of experience in clinical research coordination or clinical operations. Strong understanding of GCP, ICH, and FDA regulatory requirements. Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred. Fluent in English – both verbal and written communication required. Comfortable working independently in a fully remote setting across multiple time zones. Highly organized with strong attention to detail and documentation accuracy. Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.). Preferred Qualifications: Associate or Bachelor’s degree in health sciences or related field. Clinical research certification (e.g., ACRP, SoCRA). Prior experience supporting multi-site trials remotely. Bilingual proficiency is a plus. Work Schedule: Full-time (Remote), U. S. time zones (EST to PST) Perks of Working with UniTriTeam: Work with a mission-driven organization transforming the clinical research industry. Fully remote work environment with global team collaboration. Exposure to innovative research sites and a wide variety of protocols. Professional development and growth opportunities. Supportive and inclusive team culture. Why Join Us? 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Now get paid like it. Wellthy connects reliable caregivers with families who need last-minute childcare — school closures, holidays, unexpected work trips. You tell us your preferences (schedule, age of kids), we handle the rest. What's in it for you: 100% Schedule Control: Work twice a week or twice a month. As an independent care provider, you only accept the gigs that fit around your personal life, other opportunities, or commitments. Choose Your Track: Only want to work with toddlers, love babies? Great. Prefer hanging with older kids? Done. You only take opportunities you are comfortable with. Hassle-Free Pay: No awkward money conversations or waiting on Venmo. Get paid competitively and directly to your bank account. Earnings range from $15.00-$30.00 per hour, depending on location, experience, and family needs What You’ll Do (Choose Your Preferred Opportunity): Child Care: Keep kids engaged, safe, and off their screens with fun activities. Assist with basic routines (meals, naps, homework help). What we need from you: Experience: Some demonstrable experience in childcare (babysitting, siblings, nannying, daycare or volunteering counts!). Reliability: You show up on time and communicate clearly. Trust & Safety: To ensure the highest quality of care for our clients, all independent care providers must complete our comprehensive Trust & Safety onboarding process and meet all local, state, and enterprise childcare compliance standards. (CPR/First Aid certification is a plus!) Empathy: You genuinely care about helping families and hanging with kids. Ready to get paid for making a difference? Apply today to join the care network that fits your busy life. For those who require reasonable accommodations, please let us know on your application or email us at backupcare@wellthy.com. 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B2 level, MS Office skills", "qualificationsPreferred" : "German min. B2, Experience with SAP", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Join Our Team at Mercedes-Benz! Are you ready to drive your career forward with one of the most prestigious automotive brands in the world? Mercedes-Benz is looking for talented and passionate individuals to join our dynamic team. Whether you're an experienced professional or a recent graduate, we have exciting opportunities waiting for you! Why Mercedes-Benz? · Innovation: Be part of a company that leads the way in automotive technology and design. · Growth: We offer continuous learning and development opportunities to help you reach your full potential. · Culture: Join a diverse and inclusive workplace where your ideas and contributions are valued. · Impact: Work on projects that make a real difference in the automotive industry and beyond. Opportunities Available: · Purchase Requisition Services · Asset Accounting · Intercompany Accounting · Product Costing · VAN Sales Master Data · PTP Process Management What We’re Looking For: · English min. B2 level, · German min. B2 would be an asset, · Experience with SAP would be an asset, · MS Office skills (Excel, Outlook, Teams), · Excellent communication skills, · Collaborative team player attitude. If you are interested to join Mercedes-Benz Group Services Poland, apply here. We will be happy to review your resume. Drive Your Future with Mercedes-Benz! Mercedes-Benz Group Services Poland Sp. z o.o.", "summaryDescription" : "Future Opportunities at Mercedes-Benz. Manage Purchase Requisition Services. 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"Lead study design, Lead study planning, Lead study execution, Author clinical protocols, Author case report forms, Author study documents, Provide operational oversight, Ensure compliance with SOPs, Ensure compliance with GCP, Ensure compliance with regulations, Support budget development, Interpret clinical data, Oversee clinical data, Manage operational components, Manage clinical supply operations, Manage site selection, Manage vendor selection, Coordinate with partners, Serve as clinical research representative, Build relationships with investigators, Build relationships with customers, Build relationships with regulatory authorities, Drive local evidence dissemination, Incorporate regional feedback", "teamCollaboration" : "Cross-functional partners; External vendors; Internal partners; Investigators; Customers; Regulatory authorities", "projectManagementSkills" : [ "Study management" ], "domainKnowledge" : "Pelvic Health; Medical device industry; Regulated healthcare industry; 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clinical trial operations, Communication, stakeholder management, and organizational skills", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. # **A Day in the Life** We are seeking a Principal Clinical Research Specialist to serve as a Study Manager supporting Pelvic Health clinical studies across Europe, including the UK, France, Belgium, and Germany. This role offers the opportunity to lead and shape the execution of meaningful clinical research that directly impacts patient care. As a Study Manager, you will take ownership of multi-site studies from start‑up through close‑out, working closely with investigators, cross‑functional partners, and external vendors to deliver high‑quality, compliant clinical evidence in a dynamic, global environment. This is a remote position that will partner closely with the Pelvic Health clinical team based in Minneapolis, MN. Travel up to 20% is expected to support site engagement and study execution across Europe. **Responsibilities may include the following and other duties may be assigned:** * Lead the design, planning, and execution of registered and non‑registered Pelvic Health clinical studies, including authorship of clinical protocols, case report forms, and related study documents * Provide end‑to‑end operational oversight of multi‑site clinical trials, ensuring compliance with SOPs, GCP, and country‑specific regulations, and supporting clinical trial budget development as needed * Interpret and oversee clinical investigation data to support medical evidence generation, regulatory submissions, and new or expanded device applications * Manage key operational components of clinical studies, including clinical supply operations, site and vendor selection, and cross‑functional coordination with internal and external partners * Serve as a clinical research representative within the assigned region, building strong relationships with investigators, customers, and regulatory authorities, while driving local evidence dissemination and incorporating regional feedback into study execution **Required Knowledge and Experience:** * Extensive experience managing multi‑site, international clinical studies within the medical device or regulated healthcare industry, with demonstrated Study Manager–level accountability * Strong working knowledge of ICH‑GCP, ISO 14155, EU MDR, UK clinical research requirements, and applicable country‑specific regulations, with hands‑on application in study execution * Prior experience authoring and reviewing clinical study documentation, including protocols, CRFs, and clinical reports, and interpreting clinical data to support evidence generation and regulatory needs * Demonstrated ability to manage clinical trial operations, including vendor and site oversight, clinical supplies, budgets, and cross‑functional collaboration in a global environment * Strong communication, stakeholder management, and organizational skills, with the ability to work independently in a remote role **Physical Job Requirements** The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. # **Benefits & Compensation** **Medtronic offers a competitive Salary and flexible Benefits Package** A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: United Kingdom: 64,800.00 GBP - 97,200.00 GBP | This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). # **About Medtronic** # We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity [here](http://www.medtronic.com)", "summaryDescription" : "Principal Clinical Research Specialist at Medtronic. Skills: Study Management, Clinical Research, Regulatory Compliance. Lead study design. 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Are you ready to make a difference in the world of clinical research in a company that follows the science and turns ideas into 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 been delivering the best value to patients for more than 60 years. We advance science to develop life-changing medicines. In Cell Therapy Site Management & Monitoring (SMM), we partner closely with investigators and internal teams to initiate, run and close clinical studies efficiently and compliantly, so patients can access innovative treatments sooner. **What you’ll do** As a Clinical Research Associate (CRA), you will be central to our local study teams. You will play a key role in delivering start‑up and monitoring for new, technically advanced cell therapy studies. You will work alongside Local Study Managers and peers to meet milestones reliably and ethically. You'll be the primary contact for study sites, responsible for monitoring study conduct and ensuring compliance with international guidelines and local regulations. With opportunities for growth and additional responsibilities, this role is perfect for those looking to advance their career in clinical research! This is a full time, 12-month contract position based in Sydney, reporting to the Senior Director, SMM Cell Therapy. You’ll work remotely, travelling to sites and Head office in Sydney as needed. **Key Responsibilities:** * Contribute to selection of potential investigators and support site feasibility. * Manage study start up and regulatory maintenance, including preparing and submitting documents. * Train and support site staff on study requirements, maintain inspection readiness and ensure completion of mandatory trainings. * Initiate, monitor and close study sites in line with AstraZeneca Procedural Documents, protocols and local regulations. * Perform monitoring visits and data checks per the Monitoring Plan, including Source Data Review, Source Data Verification, Case Report Form review, and drug accountability. * Maintain study systems and documentation (e.g., Clinical Trial Management System and electronic Trial Master File) * Report Serious Adverse Events promptly, and support audits and inspections. **Essential for the role:** * Bachelors degree in related discipline, preferably in life science, or equivalent qualification * 1-2 years experience working at CRA level with independent monitoring experience, including site initiation, routine monitoring and close-out. * Strong knowledge of international guidelines ICH‐GCP and good knowledge of Australian regulatory requirements, with the ability to apply these in day-to-day monitoring. * Sound medical knowledge and ability to learn relevant AZ Therapeutic Areas. * Demonstrated experience with Clinical Trial Management Systems and electronic TMF; familiarity with Veeva Clinical Vault or equivalent. * Demonstrated ability to prioritize and manage multiple tasks with conflicting deadlines. * Ability to travel for monitoring visits across Australia with current driving licence. * Clear, confident communication and collaboration skills, with attention to detail and sound judgement in a fast‑paced environment. **Desirable:** * Manages change positively, seeing opportunities to grow. * Ability to look for and champion continuous improvement to deliver high quality trials with reduced budget and in less time. * Oncology or similarly complex monitoring experience. * Experience within a pharmaceutical sponsor environment and comfort working with ambiguity beyond prescribed Contract Research Organisation processes. * Familiarity with risk‑based and remote monitoring approaches and related tools. **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. **Guidance on AI use:** We support you using AI tools responsibly in the recruitment process in order for you to 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** 11-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 Research Associate at AstraZeneca. Skills: Clinical trial monitoring, Site management, Regulatory compliance. Contribute to investigator selection. 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"mid", "dataQualityScore" : 0.8888889, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biopharmaceutical" }, { "id" : "6a2ca67b74d8ee00a09bbb92", "title" : "Senior Clinical Research Associate (CRA)", "company" : "MapLight Therapeutics", "industry" : "Biotech", "salary" : { "min" : 145000.0, "max" : 160000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Remote", "locations" : [ "Remote" ], "timestamp" : "2026-06-15T09:46:26.220", "fingerprint" : "e6222fe5fee75db746ffd4276c7177d64648366f82cc503d763eaad44714cc33", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5255575008", "externalId" : "5255575008", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "EDC, CTMS, ETMF, ECOA, EMR, Microsoft Office", "professionalSkills" : [ "Site monitoring", "Site management", "Data integrity", "Risk management", "Study oversight", "Protocol compliance", "Process improvement", "Study document development" ], "hardSkillsList" : [ "Investigator site monitoring", "Investigator site management", "Centralized monitoring", "Risk-based monitoring", "Trial Master File", "Investigator Site File", "Regulatory requirements", "Clinical systems maintenance" ], "hardSkills" : [ { "name" : "Investigator site monitoring", "level" : "intermediate" }, { "name" : "Investigator site management", "level" : "intermediate" }, { "name" : "Centralized monitoring", "level" : "intermediate" }, { "name" : "Risk-based monitoring", "level" : "intermediate" }, { "name" : "Trial Master File", "level" : "intermediate" }, { "name" : "Investigator Site File", "level" : "intermediate" }, { "name" : "Regulatory requirements", "level" : "intermediate" }, { "name" : "Clinical systems maintenance", "level" : "intermediate" } ], "majorSkills" : "Clinical monitoring, Site management, ICH GCP, Data integrity", "majorSkillsList" : [ "Clinical monitoring", "Site management", "ICH GCP", "Data integrity" ], "coreResponsibilities" : "Perform quality Investigator site monitoring, Perform compliant Investigator site monitoring, Perform relationship-driven Investigator site management, Ensure subject safety, Ensure data integrity, Contribute to risk management, Contribute to inspection readiness, Collaborate with internal stakeholders, Collaborate with external CRO partners, Collaborate with vendor partners, Ensure quality study oversight, Manage assigned Investigator sites, Maintain positive relationships site personnel, Prepare Pre-Study monitoring visits, Conduct Pre-Study monitoring visits, Prepare Initiation monitoring visits, Conduct Initiation monitoring visits, Prepare Interim monitoring visits, Conduct Interim monitoring visits, Prepare Closeout monitoring visits, Conduct Closeout monitoring visits, Support study team milestones, Perform centralized monitoring activities, Ensure timely resolution action items, Oversight study data quality, Oversight study data flow, Proactively identify study risks, Mitigate study risks, Manage study risks, Proactively identify study issues, Mitigate study issues, Manage study issues, Maintain quality documentation site management, Maintain compliant documentation site management, Maintain monitoring visit reports, Maintain centralized monitoring reports, Maintain site contact reports, Reconcile Trial Master File, Reconcile Investigator Site File, Serve as MapLight point contact, Support protocol compliance, Support streamlined communications, Support timely responses site staff needs, Support training needs, Support study team inspections, Support Investigator sites inspections, Support study team audits, Support Investigator sites audits, Perform other assigned tasks, Support study team development study documents, Support study team development study procedures, Support development study monitoring plan, Support maintenance study monitoring plan, Support development study templates, Support maintenance study templates, Support development study tools, Support maintenance study tools, Support set-up study systems, Support testing study systems, Support maintenance study systems, Support related supporting documents, Support eCRF Completion Guidelines, Reconcile Trial Master File assigned sites, Reconcile Investigator Site File assigned sites, Maintain current knowledge regulatory requirements, Maintain current knowledge industry best practices, Support development process improvement monitoring function, Support development SOPs, Support revision SOPs, Support development processes, Support revision processes, Support development templates, Support revision templates, Support development tools, Support revision tools, Support development plans, Support revision plans, Contribute maintenance clinical systems, Contribute improvement clinical systems, Embody MapLight’s core values, Demonstrate MapLight’s core values", "teamCollaboration" : "Cross-functional internal stakeholders; External CRO partners; Vendor partners; Clinical Operations; Medical Monitoring; Data Management; Supply Chain; Clinical Compliance; Quality; Investigator sites", "projectManagementSkills" : [ "Study start up", "Study close out", "Study milestones" ], "domainKnowledge" : "Central nervous system disorders; Optogenetics; In vivo physiology; Spatial transcriptomics; Psychiatric symptoms; CNS; Neuropsychiatry; In-patient schizophrenia; Alzheimer’s disease psychosis; Alzheimer's disease agitation; Good Clinical Practices; ICH GCP; ALCOA+", "domainList" : [ "central-nervous-system-disorders", "optogenetics", "in-vivo-physiology", "spatial-transcriptomics", "psychiatric-symptoms", "cns", "neuropsychiatry", "in-patient-schizophrenia", "alzheimer-s-disease-psychosis", "alzheimer-s-disease-agitation", "good-clinical-practices", "ich-gcp", "alcoa" ], "domainSpecificKnowledge" : [ "Central nervous system disorders", "Optogenetics", "In vivo physiology", "Spatial transcriptomics", "Psychiatric symptoms", "CNS", "Neuropsychiatry", "In-patient schizophrenia", "Alzheimer’s disease psychosis", "Alzheimer's disease agitation", "Good Clinical Practices", "ICH GCP", "ALCOA+" ], "toolProficiency" : [ "EDC", "CTMS", "ETMF", "ECOA", "EMR", "Microsoft Word", "Microsoft Excel", "Microsoft PowerPoint", "Microsoft Outlook" ], "communicationSkills" : "Oral communication; Written communication", "documentationSkills" : "Monitoring visit reports; Centralized monitoring reports; Site contact reports; Trial Master File; Investigator Site File; ECRF Completion Guidelines", "problemSolvingSkills" : "Risk management; Risk mitigation", "specialRequirements" : "Up to 75% travel, Travel regional, Travel outside region, Periodic travel meetings", "outcomesObjectives" : "Ensure subject safety; Ensure data integrity; Contribute risk management; Contribute inspection readiness; Ensure quality study oversight; Meet study milestones", "qualificationsBasic" : "5 plus years clinical trial industry, 4 years clinical monitoring experience, Working knowledge GCPs, Working knowledge ALCOA+, Working knowledge pertinent regulations, Ability to build relationships, Ability to engage collaboratively, Interpersonal communication skills, Oral communication skills, Written communication skills, Ability to work independently, Ability to work proactively, Core understanding medical terminology, Core understanding clinical trial activities, High attention to detail, Focus on quality, Focus on compliance, Experience working clinical software systems, Proficiency Microsoft Office applications, Ability to travel independently", "qualificationsPreferred" : "CNS experience strongly preferred, Neuropsychiatry experience strongly preferred, In-patient schizophrenia experience preferred, Alzheimer’s disease psychosis experience preferred, Alzheimer's disease agitation experience preferred, Experience working smallerging biotech ideal, Experience managing multiple Investigator sites, Experience managing multiple studies simultaneously, Location near major airport preferred", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. Location: This is a remote role located in the Texas OR Arizona region. Travel: Position will require up to 75% travel with potential to be higher at times of peak activity. Every effort will be made to keep travel regional but travel outside of a region may be required on occasion. Additional periodic travel for meetings is also expected. What You’ll Do: The Sr. CRA will perform quality and compliant Investigator site monitoring and relationship-driven Investigator site management in line with MapLight’s SOPs, our Mission, Vision, and Values, as well as industry quality and regulatory best practices (ICH GCP). The CRA will perform on-site monitoring and centralized monitoring to ensure subject safety, the highest data integrity, and contribute to proactive risk management and inspection readiness. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendor partners to ensure quality study oversight from study start up through close out. CNS and/or neuropsychiatry, specifically in-patient schizophrenia and/or Alzheimer’s disease psychosis or Alzheimer's disease agitation experience strongly preferred. Responsibilities: Effectively manage assigned Investigator sites and maintain positive relationships with site personnel. Prepare for and conduct Pre-Study, Initiation, Interim and Closeout monitoring visits in accordance with MapLight SOPs and procedures, regulatory requirements and industry guidelines and best practices (ICH GCP). Support the study team in meeting study milestones (site activation, DSMB meetings, database lock, etc.). Perform centralized monitoring activities between on-site visits to ensure timely resolution of action items, oversight of study data quality and flow, and proactively identify and mitigate/manage study risks and issues. Maintain quality and compliant documentation related to all aspects of site management including quality and ALCOA+ compliant monitoring visit reports, centralized monitoring reports, site contact reports, Trial Master File/Investigator Site File, etc. Serve as the main MapLight point of contact for Investigator sites to support protocol compliance, streamlined communications, timely responses to site staff needs, and training needs. Support the study team and Investigator sites during inspections or audits, as needed. Perform other assigned tasks, as requested. Support the study team(s) in development of study documents and procedures. As requested: Support the development and maintenance of the study monitoring plan, templates, and tools. Support the set-up, testing, and maintenance of study systems (EDC, eCOA, IRT, etc.) as well as related supporting documents (manuals, eCRF Completion Guidelines, etc.) in collaboration with MapLight and CRO/vendor study team members. Continually review and reconcile the Trial Master File and Investigator Site File for assigned sites to ensure inspection readiness. Maintain current knowledge of regulatory requirements and industry best practices related to monitoring, including centralized monitoring and risk-based monitoring. Support development and process improvement for the MapLight monitoring function. Support development and revision of SOPs, processes, templates, tools, and plans with the aim of continual improvement and streamlining. Contribute to the maintenance and improvement of clinical systems to drive process improvement and efficiency. Embody and demonstrate MapLight’s core values of Integrity, Collaboration, Bravery, and Dedication. Qualifications: Approximately 5 plus years in the clinical trial industry with at least 4 years of clinical monitoring experience including complex therapeutic areas, in-patient trials, and blinded trials. CNS and/or neuropsychiatry, specifically in-patient schizophrenia and/or Alzheimer’s disease psychosis or Alzheimer's disease agitation experience strongly preferred. Experience working in small/emerging biotech is ideal Experience managing multiple Investigator sites and multiple studies simultaneously. Willingness to travel nationally to assigned Investigator sites as needed for required visits. Ability to build relationships between Investigator sites and MapLight to foster strong collaboration, trust, and positive working relationships. Strong working knowledge of Good Clinical Practices (GCPs), ALCOA+, and pertinent regulations. Ability to engage collaboratively with internal and external stakeholders in a professional manner. Strong interpersonal, oral, and written communication skills. A self-starter with the ability to work independently and proactively. Willingness to be a “team player” and take on additional responsibilities as requested. Demonstrates core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan. High attention to detail and focus on quality and compliance in all aspects of assigned work. Experience working in various clinical software systems (EDC, CTMS, eTMF, eCOA, EMR). Proficiency with Microsoft Office applications (Word, Excel, PowerPoint, Outlook). Ability to travel independently by air, car and/or train. Location near a major airport preferred. Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD&D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave. Salary Range $145,000—$160,000 USD EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.", "summaryDescription" : "Senior Clinical Research Associate (CRA) at MapLight Therapeutics. Skills: Clinical monitoring, Site management, ICH GCP, Data integrity. Perform quality Investigator site monitoring. Perform compliant Investigator site monitoring", "postedDate" : "2026-06-14T08:57:42.161", "createdAt" : "2026-06-14T08:57:42.161", "lastUpdated" : "2026-06-15T09:46:26.220", "ingestTimestamp" : "2026-06-14T08:57:42.161", "mongoId" : "6a2ca67b74d8ee00a09bbb92", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 145000, "salaryAnnualMax" : 160000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Investigator site monitoring", "Investigator site management", "Centralized monitoring", "Risk-based monitoring", "Trial Master File", "Investigator Site File", "Regulatory requirements", "Clinical systems maintenance", "Clinical monitoring", "Site management", "ICH GCP", "Data integrity", "Site monitoring", "Risk management", "Study oversight", "Protocol compliance", "Process improvement", "Study document development", "Study start up", "Study close out", "Study milestones", "Central nervous system disorders", "Optogenetics", "In vivo physiology", "Spatial transcriptomics", "Psychiatric symptoms", "CNS", "Neuropsychiatry", "In-patient schizophrenia", "Alzheimer’s disease psychosis", "Alzheimer's disease agitation", "Good Clinical Practices", "ALCOA+", "EDC", "CTMS", "ETMF", "ECOA", "EMR", "Microsoft Word", "Microsoft Excel", "Microsoft PowerPoint", "Microsoft Outlook" ], "skillCount" : 42, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2af78174d8ee00a073d5c5", "title" : "Senior Clinical Research Manager", "company" : "AstraZeneca", "salary" : { "min" : 650000.0, "max" : 1100000.0, "currency" : "CNY", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Clinical Research Manager in China, adjusted for seniority, industry, and company size." }, "location" : "China", "locations" : [ "China" ], "timestamp" : "2026-06-15T00:15:28.747", "fingerprint" : "5fa2ed340a912b5cab8dcdde065b41537090257bc536c0478265b35658ba7ae9", "source" : "workday", "language" : "en", "applyUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/China/Senior-Clinical-Research-Manager_R-254309", "externalId" : "R-254309", "locationPoint" : "35.8617,104.1954", "structuredLocations" : [ { "country" : "China", "continent" : "as", "workMode" : "onsite" } ], "locationText" : "China", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "professionalSkills" : [ "Study delivery", "Hospital strategic cooperation", "Clinical investigator network" ], "hardSkillsList" : [ "Site monitoring", "Feasibility work", "Resource allocation", "Talent development" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Site monitoring", "level" : "intermediate" }, { "name" : "Feasibility work", "level" : "intermediate" }, { "name" : "Resource allocation", "level" : "intermediate" }, { "name" : "Talent development", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Cell therapy studies, Team management, Clinical research", "majorSkillsList" : [ "Cell therapy studies", "Team management", "Clinical research" ], "coreResponsibilities" : "Lead, guide, evaluate, and develop the team, Ensure quality execution and delivery of site monitoring, Build team spirit, Contribute to efficient cell therapy organization, Develop and enhance cell therapy specific training program, Ensure adequate resources allocation for studies, Manage resource conflicts, Build and retain an efficient team, Provide leadership to team members, Provide monitoring to team members, Contribute to quality improvement of study processes, Contribute to quality improvement of other procedures, Oversight relevant system maintained by CRA, Review monitoring reports of CRA, Review follow-up letters of CRA, Perform accompanied site visits for CRA, Assist study team in forecasting study timelines, Assist study team in forecasting study resources, Assist study team in forecasting study recruitment, Assist study team in forecasting study materials, Assist study team in forecasting study drugs, Contribute to high quality feasibility work, Provide guidance to study team on major study, Resolve key issues identified, Contribute to development strategic cooperation of clinical investigator, Maintain good relationship with key sites, Ensure team complying with company policy, Ensure team complying with code of conduct, Manage junior/less experienced CRM, Coach junior/less experienced CRM, Develop junior/less experienced CRM", "teamCollaboration" : "Work closely with team leader; Work with study team; Work with key sites", "projectManagementSkills" : [ "Study timelines", "Resource allocation" ], "domainKnowledge" : "Cell therapy; ICH guidelines; GCP guidelines; Local regulations", "domainList" : [ "cell-therapy", "ich-guidelines", "gcp-guidelines", "local-regulations" ], "domainSpecificKnowledge" : [ "Cell therapy", "ICH guidelines", "GCP guidelines", "Local regulations" ], "documentationSkills" : "Monitoring reports; Follow-up letters", "continuousLearning" : "Training program", "problemSolvingSkills" : "Resolve key issues", "outcomesObjectives" : "Ensure excellent cell therapy study performance; Ensure quality execution and delivery; Build and retain an efficient team; Contribute to quality improvement; Maintain good relationship with key sites; Ensure performance aligns with team requirement", "qualificationsBasic" : "Manage a CRA team, Ensure excellent cell therapy study performance, Comply with AZ Procedural Documents, Comply with ICH guidelines, Comply with GCP guidelines, Comply with relevant local regulations, Develop talents by providing coaching, Develop talents by providing training, Develop talents by providing support, Develop talents by providing monitoring, Contribute to cell therapy study resource allocation, Manage junior/less experienced CRM", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Senior Clinical Research Manager (Sr. CRM) is responsible to manage a CRA team and to ensure excellent cell therapy study performance at site level, complying with AZ Procedural Documents, international guidelines such as ICH and GCP as well asrelevant local regulations. As line manager of CRA, he/she is accountable for developing talents by providing continuously coaching, training, support and monitoring to CRA. Contributes to cell therapy study resource allocation to ensure efficient work of study delivery. Sr. CRM contributes to hospital strategic cooperation for business continuous.Sr. CRM is also responsible to manage junior/less experienced CRM if applicable. **Typical Accountabilities** • Lead, guide, evaluate and develop the team, to ensure the quality execution and delivery of the site monitoring in the cell therapy sites. Build up the team spirit and contribute to efficient cell therapy organisation by working closely with team leader. • Develop and enhance cell therapy specific training program to CRA. • Ensuring adequate resources allocation for the cell therapy studies assigned and manage resource conflicts. • Accountable for build and retain an efficient team by providing leadership and monitoring to team members. • Contribute to the quality improvement of the cell therapy study processes and other procedures. Oversight relevant system which maintained by CRA with high quality. Review of monitoring reports/follow up letters of CRA as per study monitoring and/or local clinical quality management plans. Perform necessary accompanied site visits for CRA. • Assist study team in forecasting cell therapy study timelines, resources, recruitment, study materials and drugs. Contribute to high quality feasibility work. Provide guidance to study team on major study commitments including resolving any key issues identified. • Contribute to development strategic cooperation of clinical investigator network and maintain good relationship with key sites as assigned. • Ensure team complying with company policy and code of conduct. • Manage, coach and develop junior/less experienced CRM if applicable, ensuring their performance aligns with team requirement 【AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised. 阿斯利康是一家提供平等机会的企业，我们将考虑所有符合条件的求职者就业。不因残疾、性别或性取向、怀孕或产假状况、种族或民族或族裔出身、年龄、宗教或信仰、性别认同或变更、婚姻或伴侣关系、受保护的退伍军人身份（如果适用）及任何其他受法律保护的特征而产生歧视。】 **Date Posted** 11-6月-2026 **Closing Date** 29-6月-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" : "Senior Clinical Research Manager at AstraZeneca. Skills: Cell therapy studies, Team management, Clinical research. Lead, guide, evaluate, and develop the team. Ensure quality execution and delivery of site monitoring", "postedDate" : "2026-06-12T04:57:12.200", "createdAt" : "2026-06-12T04:57:12.194", "lastUpdated" : "2026-06-15T00:15:28.747", "ingestTimestamp" : "2026-06-12T04:57:12.194", "mongoId" : "6a2af78174d8ee00a073d5c5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/China/Senior-Clinical-Research-Manager_R-254309", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Site monitoring", "Feasibility work", "Resource allocation", "Talent development", "Leadership", "Mentoring", "Cell therapy studies", "Team management", "Clinical research", "Study delivery", "Hospital strategic cooperation", "Clinical investigator network", "Study timelines", "Cell therapy", "ICH guidelines", "GCP guidelines", "Local regulations" ], "skillCount" : 17, "jobCategory" : "other", "seniorityLevel" : "manager", "dataQualityScore" : 1.0, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false }, { "id" : "6a2b123b74d8ee00a07680c9", "title" : "Clinical Research Associate", "company" : "Biomapas", "industry" : "Pharmaceuticals", "salary" : { "min" : 1500000.0, "max" : 2500000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a mid-level Clinical Research Associate in India, adjusted for the biotech industry and remote work." }, "location" : "Remote", "locations" : [ "Remote" ], "timestamp" : "2026-06-15T00:42:36.247", "fingerprint" : "10b85de9201918e4471e54076af00a216d9eba77ea5db5eae6724667213f4036", "source" : "workable", "language" : "en", "applyUrl" : "https://apply.workable.com/j/6CD2309A3D/apply", "externalId" : "6CD2309A3D", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "employmentType" : "FULL_TIME", "minimumEducation" : "University degree", "technicalSkills" : "MS Office, EDC", "professionalSkills" : [ "Clinical research", "Protocol knowledge", "Regulatory requirements" ], "hardSkillsList" : [ "Site monitoring", "Site management", "Feasibilities", "Study documentation", "Regulatory document review", "Clinical trial documents", "Budget negotiation" ], "hardSkills" : [ { "name" : "Site monitoring", "level" : "intermediate" }, { "name" : "Site management", "level" : "intermediate" }, { "name" : "Feasibilities", "level" : "intermediate" }, { "name" : "Study documentation", "level" : "intermediate" }, { "name" : "Regulatory document review", "level" : "intermediate" }, { "name" : "Clinical trial documents", "level" : "intermediate" }, { "name" : "Budget negotiation", "level" : "intermediate" } ], "majorSkills" : "Clinical Research Associate, Site monitoring, Regulatory compliance", "majorSkillsList" : [ "Clinical Research Associate", "Site monitoring", "Regulatory compliance" ], "coreResponsibilities" : "Study site monitoring, Study site management, Perform feasibilities, Support start-up phase, Create study documentation, Maintain study documentation, Ensure clinical trials conducted, Administer protocol training, Administer study training, Perform regulatory document review, Prepare clinical trial documents, Store correspondence, Archive correspondence, Negotiate study budgets, Assist in agreements", "domainKnowledge" : "Clinical research; GCP; ICH-GCP", "domainList" : [ "clinical-research", "gcp", "ich-gcp" ], "domainSpecificKnowledge" : [ "Clinical research", "GCP", "ICH-GCP" ], "toolProficiency" : [ "MS Office", "EDC" ], "documentationSkills" : "Study documentation; Clinical documentation", "continuousLearning" : "Professional growth; Career opportunities", "qualificationsBasic" : "University degree in Life Science, Fluent English and local language, Independent monitoring experience as a CRA, In depth therapeutic and protocol knowledge, Deep knowledge in clinical research regulatory requirements, Excellent skills in MS Office, Excellent skills in EDC, Excellent skills in other clinical trial related systems and platforms, Attention to detail, Time-management skills", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "### Join our dynamic team at Biomapas as a **Clinical Research Associate (CRA) in Ukraine.** Your role will be crucial in overseeing clinical trials and ensuring that they are conducted in compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. **Role is combined with office and home-based in Ukraine. All CV's needs to be submitted in English language.** ### **Responsibilities:** * Study site monitoring and management (site selection, initiation, monitoring and close-out visits) * Perform feasibilities and support start-up phase * Create and maintain required study documentation (site management, monitoring, etc.) * Ensure that clinical trials are conducted according to requirements (protocol, ICH-GCP, etc.) * Administer protocol and related study training to assigned sites * Perform regulatory document review * Prepare clinical trial documents and store, archive correspondence * Negotiate study budgets with potential investigators/sites, assit in agreements **Requirements** * University degree in Life Science field * Fluent English and local language * Independent monitoring experience as a CRA * In depth therapeutic and protocol knowledge * Deep knowledge in clinical research regulatory requirements (GCP and ICH) * Excellent skills in MS Office, EDC and other clinical trial related systems and platforms * Attention to detail and time-management skills **Benefits** * Professional growth and career opportunities * International team and environment * Bonus based on annual performance * Personal accident and business trip insurance * Additional health insurance * Remote/home based * Complimentary health and wellness benefits, such as influenza vaccines * Rewarding referral policy * Workplace establishment allowance (fully remote) * Team building, global meetings, B active events", "summaryDescription" : "Clinical Research Associate at Biomapas. Skills: Clinical Research Associate, Site monitoring, Regulatory compliance. Study site monitoring. Study site management", "postedDate" : "2026-06-11T00:00:00.000", "createdAt" : "2026-06-12T04:55:14.170", "lastUpdated" : "2026-06-15T00:42:36.247", "ingestTimestamp" : "2026-06-12T04:55:14.170", "mongoId" : "6a2b123b74d8ee00a07680c9", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://apply.workable.com/j/6CD2309A3D", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Site monitoring", "Site management", "Feasibilities", "Study documentation", "Regulatory document review", "Clinical trial documents", "Budget negotiation", "Clinical Research Associate", "Regulatory compliance", "Clinical research", "Protocol knowledge", "Regulatory requirements", "GCP", "ICH-GCP", "MS Office", "EDC" ], "skillCount" : 16, "jobCategory" : "other", "jobSubcategory" : "pharmaceuticals", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a2a53f474d8ee00a0600be0", "title" : "Clinical Research Coordinator II", "company" : "Iterative Health", "industry" : "Healthcare Technology", "salary" : { "min" : 68000.0, "max" : 92000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Research Coordinator II in New Albany, United States, adjusted for industry and company size." }, "location" : "New Albany, Indiana, United States", "locations" : [ "New Albany", "Indiana", "United States" ], "timestamp" : "2026-06-14T19:40:28.839", "fingerprint" : "8420bc151219004651aba09df112d2835e3dab7dc153905805311870ed070880", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/iterativehealth/jobs/4687399006", "externalId" : "4687399006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New Albany", "state" : "Indiana", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.2856247,-85.8241312" } ], "locationText" : "New Albany, Indiana, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Associate's", "experienceMinYears" : 3, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "professionalSkills" : [ "Protocol management", "Data entry", "Data verification", "Quality control" ], "hardSkillsList" : [ "ECGs", "Blood draws", "Specimen processing", "Specimen shipping" ], "hardSkills" : [ { "name" : "ECGs", "level" : "intermediate" }, { "name" : "Blood draws", "level" : "intermediate" }, { "name" : "Specimen processing", "level" : "intermediate" }, { "name" : "Specimen shipping", "level" : "intermediate" } ], "majorSkills" : "Clinical research, Patient recruitment, Protocol adherence", "majorSkillsList" : [ "Clinical research", "Patient recruitment", "Protocol adherence" ], "coreResponsibilities" : "Manage clinical trials, Coordinate study visits, Lead patient recruitment, Perform chart reviews, Discuss protocols with patients, Verify informed consent, Schedule patient research visits, Conduct patient visits, Dispense study medication, Collect vital signs, Perform ECGs, Process specimens, Ship specimens, Enter study information into CTMS, Maintain study files, Enter data, Act as point of contact, Adhere to Research SOPs, Adhere to Good Clinical Practices, Adhere to study protocols, Communicate with CRO, Communicate with sponsor, Communicate with participants, Communicate with Site Manager, Communicate with central team, Communicate with PI, Resolve sponsor issues, Resolve CRO issues, Review safety data, Maintain inventory of supplies, Contribute to status updates, Implement ideas to improve site performance, Assist with data verification, Assist with quality control, Resolve data queries, Schedule monitor visits, Prepare for monitor visits, Protect human research participants, Cooperate with compliance efforts, Cooperate with monitoring efforts, Complete case report forms, Review case report forms", "teamCollaboration" : "Work with other employees; Work with customers; Work with suppliers; Team contributor; Coordinate work efforts", "domainKnowledge" : "Clinical trials; Gastrointestinal therapies; Hepatology therapies; Good Clinical Practices; IATA regulations; FDA guidelines; Human research participants", "domainList" : [ "clinical-trials", "gastrointestinal-therapies", "hepatology-therapies", "good-clinical-practices", "iata-regulations", "fda-guidelines", "human-research-participants" ], "domainSpecificKnowledge" : [ "Clinical trials", "Gastrointestinal therapies", "Hepatology therapies", "Good Clinical Practices", "IATA regulations", "FDA guidelines", "Human research participants" ], "toolProficiency" : [ "CTMS" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Clinical documentation; Source documentation; Progress notes; Case report forms; Investigational accountability forms", "problemSolvingSkills" : "Problem solving", "specialRequirements" : "Lift up to 25 pounds", "qualificationsBasic" : "3 years clinical research experience, IBD experience", "qualificationsPreferred" : "Medical Assistant preferred, LPN preferred, Associate's degree preferred, Bachelor's degree preferred, Experience in phlebotomy preferred", "workSiteFlexibility" : "Onsite", "rawDescription" : "Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. Responsibilities: Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals Schedule all patient research visits and procedures consistent with protocol requirements Conduct patient visits as outlined within each study protocol Dispense study medication, collect vital signs and perform ECGs Perform blood draws, process and ship specimens per study protocol and IATA regulations Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines Act as point of contact for study participants Adhere to Research SOPs, Good Clinical Practices, and the study protocols Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently Ensure all safety data is reviewed by the PI in a timely manner Maintain inventory of study equipment and supplies onsite at all times Contribute to status updates to management; contribute and implement ideas to improve site performance Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality. Schedule and prepare for monitor visits Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy Iterative Health Expectations All employees are expected to: Perform quality work within deadlines with or without direct supervision Interact professionally with other employees, customers and suppliers Work effectively as a team contributor on all assignments Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations Qualifications Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred Minimum 3 years of clinical research experience IBD experience is a must Ability to own issues and problem solve independently Experience in phlebotomy preferred Strong written and verbal communication skils Ability to read, interpret, and apply clinic policies and research protocols Ability to use standard office software Must be able to lift up to 25 pounds At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health. At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.", "summaryDescription" : "Clinical Research Coordinator II at Iterative Health. Skills: Clinical research, Patient recruitment, Protocol adherence. Manage clinical trials. Coordinate study visits", "postedDate" : "2026-06-12T00:05:58.621", "createdAt" : "2026-06-12T00:05:58.621", "lastUpdated" : "2026-06-14T19:40:28.839", "ingestTimestamp" : "2026-06-12T00:05:58.621", "mongoId" : "6a2a53f474d8ee00a0600be0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 68000, "salaryAnnualMax" : 92000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "ECGs", "Blood draws", "Specimen processing", "Specimen shipping", "Clinical research", "Patient recruitment", "Protocol adherence", "Protocol management", "Data entry", "Data verification", "Quality control", "Clinical trials", "Gastrointestinal therapies", "Hepatology therapies", "Good Clinical Practices", "IATA regulations", "FDA guidelines", "Human research participants", "CTMS" ], "skillCount" : 19, "jobCategory" : "other", "jobSubcategory" : "clinical-services", "dataQualityScore" : 1.0, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare Technology" }, { "id" : "6a2a53f474d8ee00a0600bdf", "title" : "Clinical Research Coordinator II", "company" : "Iterative Health", "industry" : "Healthcare", "salary" : { "min" : 68000.0, "max" : 92000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Clinical Research Coordinator II in Hermitage, United States, adjusted for mid-seniority and healthcare industry." }, "location" : "Hermitage, TN", "locations" : [ "Hermitage", "TN" ], "timestamp" : "2026-06-14T19:20:57.936", "fingerprint" : "fc7a240e8e81a329b0fb48fcc586d5ff291c899867f82044690ea6e5d36ad787", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/iterativehealth/jobs/4687408006", "externalId" : "4687408006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Hermitage", "state" : "Tennessee", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "36.1961664,-86.6224959" } ], "locationText" : "Hermitage, Tennessee, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Associate's", "experienceMinYears" : 3, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "professionalSkills" : [ "Clinical research", "Protocol management", "Data entry", "Data integrity", "Data query resolution" ], "hardSkillsList" : [ "Perform ECGs", "Blood draws", "Specimen processing", "Specimen shipping", "Chart reviews", "Informed consent", "Case report forms" ], "hardSkills" : [ { "name" : "Perform ECGs", "level" : "intermediate" }, { "name" : "Blood draws", "level" : "intermediate" }, { "name" : "Specimen processing", "level" : "intermediate" }, { "name" : "Specimen shipping", "level" : "intermediate" }, { "name" : "Chart reviews", "level" : "intermediate" }, { "name" : "Informed consent", "level" : "intermediate" }, { "name" : "Case report forms", "level" : "intermediate" } ], "majorSkills" : "Clinical trials, Patient recruitment, Protocol adherence", "majorSkillsList" : [ "Clinical trials", "Patient recruitment", "Protocol adherence" ], "coreResponsibilities" : "Manage clinical trials, Coordinate study visits, Lead patient recruitment, Perform chart reviews, Discuss protocols with patients, Verify informed consent, Schedule patient research visits, Conduct patient visits, Dispense study medication, Collect vital signs, Perform ECGs, Perform blood draws, Process specimens, Ship specimens, Enter information into CTMS, Maintain documentation study files, Enter data, Act as point of contact, Adhere to Research SOPs, Adhere to Good Clinical Practices, Adhere to study protocols, Maintain communication with CRO, Maintain communication with sponsor, Maintain communication with participants, Maintain communication with Site Manager, Maintain communication with central team, Maintain communication with PI, Resolve sponsor issues, Resolve CRO issues, Review safety data, Maintain inventory of supplies, Contribute to status updates, Implement ideas to improve site performance, Assist with data verification, Assist with quality control, Schedule monitor visits, Prepare for monitor visits, Protect rights of participants, Protect welfare of participants, Cooperate with compliance efforts, Cooperate with monitoring efforts, Complete case report forms, Maintain case report forms, Review case report forms", "teamCollaboration" : "Work with other employees; 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The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. Responsibilities: Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals Schedule all patient research visits and procedures consistent with protocol requirements Conduct patient visits as outlined within each study protocol Dispense study medication, collect vital signs and perform ECGs Perform blood draws, process and ship specimens per study protocol and IATA regulations Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines Act as point of contact for study participants Adhere to Research SOPs, Good Clinical Practices, and the study protocols Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently Ensure all safety data is reviewed by the PI in a timely manner Maintain inventory of study equipment and supplies onsite at all times Contribute to status updates to management; contribute and implement ideas to improve site performance Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality. Schedule and prepare for monitor visits Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy Iterative Health Expectations All employees are expected to: Perform quality work within deadlines with or without direct supervision Interact professionally with other employees, customers and suppliers Work effectively as a team contributor on all assignments Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations Qualifications Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred Minimum 3 years of clinical research experience IBD experience is a must Ability to own issues and problem solve independently Experience in phlebotomy preferred Strong written and verbal communication skils Ability to read, interpret, and apply clinic policies and research protocols Ability to use standard office software Must be able to lift up to 25 pounds At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health. At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.", "summaryDescription" : "Clinical Research Coordinator II at Iterative Health. Skills: Clinical trials, Patient recruitment, Protocol adherence. Manage clinical trials. Coordinate study visits", "postedDate" : "2026-06-11T23:05:29.716", "createdAt" : "2026-06-11T23:05:29.716", "lastUpdated" : "2026-06-14T19:20:57.936", "ingestTimestamp" : "2026-06-11T23:05:29.716", "mongoId" : "6a2a53f474d8ee00a0600bdf", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 68000, "salaryAnnualMax" : 92000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Perform ECGs", "Blood draws", "Specimen processing", "Specimen shipping", "Chart reviews", "Informed consent", "Case report forms", "Clinical trials", "Patient recruitment", "Protocol adherence", "Clinical research", "Protocol management", "Data entry", "Data integrity", "Data query resolution", "Gastrointestinal therapies", "Hepatology therapies", "Good Clinical Practices", "IATA regulations", "FDA guidelines", "PHI regulations", "CTMS system" ], "skillCount" : 22, "jobCategory" : "other", "jobSubcategory" : "clinical-services", "dataQualityScore" : 1.0, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2a53f474d8ee00a0600bdd", "title" : "Clinical Research Coordinator II", "company" : "Iterative Health", "salary" : { "min" : 65000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on 2024-2025 market data for a Mid-level Clinical Research Coordinator II in Flowood, United States, within the Healthcare industry, adjusted for company size and experience." }, "location" : "Flowood, Mississippi, United States", "locations" : [ "Flowood", "Mississippi", "United States" ], "timestamp" : "2026-06-14T23:12:41.882", "fingerprint" : "9f3ae90b114b7cbec69f74ec53dba4abceaeaa2ed9ab4c7b64fac3c85e72900c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/iterativehealth/jobs/4687404006", "externalId" : "4687404006", "structuredLocations" : [ { "city" : "Flowood", "state" : "Mississippi", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.3092861,-90.1386811" } ], "locationText" : "Flowood, Mississippi, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Associate's", "experienceMinYears" : 3, "professionalSkills" : [ "Clinical trials", "Protocol management", "Data entry", "Data integrity", "Data query resolution" ], "hardSkillsList" : [ "Phlebotomy", "ECG", "Blood draws", "Specimen processing", "Specimen shipping" ], "hardSkills" : [ { "name" : "Phlebotomy", "level" : "intermediate" }, { "name" : "ECG", "level" : "intermediate" }, { "name" : "Blood draws", "level" : "intermediate" }, { "name" : "Specimen processing", "level" : "intermediate" }, { "name" : "Specimen shipping", "level" : "intermediate" } ], "majorSkills" : "Clinical research, Patient recruitment, Protocol adherence", "majorSkillsList" : [ "Clinical research", "Patient recruitment", "Protocol adherence" ], "coreResponsibilities" : "Manage clinical trial activities, Coordinate study visits, Lead patient recruitment, Perform chart reviews, Discuss protocols with patients, Verify informed consent, Schedule patient research visits, Conduct patient visits, Dispense study medication, Collect vital signs, Perform ECGs, Process specimens, Ship specimens, Enter study information into CTMS, Maintain study files, Complete case report forms, Maintain data quality, Resolve data queries, Prepare for monitor visits, Protect human research participants, Report instances of noncompliance, Review case report forms, Maintain inventory of study supplies", "teamCollaboration" : "Communicate with CRO; Communicate with sponsor; Communicate with participants; Communicate with Site Manager; Communicate with central team; Communicate with PI; Work with study team; Work with research participants", "domainKnowledge" : "Gastrointestinal; Hepatology; Good Clinical Practices; FDA guidelines; IATA regulations", "domainList" : [ "gastrointestinal", "hepatology", "good-clinical-practices", "fda-guidelines", "iata-regulations" ], "domainSpecificKnowledge" : [ "Gastrointestinal", "Hepatology", "Good Clinical Practices", "FDA guidelines", "IATA regulations" ], "toolProficiency" : [ "CTMS", "IATA regulations" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Clinical documentation; Source documentation; Progress notes; Case report forms; Informed consent documentation", "problemSolvingSkills" : "Problem solve independently", "specialRequirements" : "Lift up to 25 pounds", "outcomesObjectives" : "Meet enrollment targets; Achieve enrollment goals; Meet data query resolution times", "qualificationsBasic" : "3 years clinical research experience, IBD experience, Lift up to 25 pounds", "qualificationsPreferred" : "Medical Assistant degree, LPN, Associate's degree, Bachelor's degree, Clinical or scientific-related discipline, Phlebotomy experience", "workSiteFlexibility" : "Onsite", "rawDescription" : "Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. Responsibilities: Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals Schedule all patient research visits and procedures consistent with protocol requirements Conduct patient visits as outlined within each study protocol Dispense study medication, collect vital signs and perform ECGs Perform blood draws, process and ship specimens per study protocol and IATA regulations Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines Act as point of contact for study participants Adhere to Research SOPs, Good Clinical Practices, and the study protocols Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently Ensure all safety data is reviewed by the PI in a timely manner Maintain inventory of study equipment and supplies onsite at all times Contribute to status updates to management; contribute and implement ideas to improve site performance Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality. Schedule and prepare for monitor visits Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy Iterative Health Expectations All employees are expected to: Perform quality work within deadlines with or without direct supervision Interact professionally with other employees, customers and suppliers Work effectively as a team contributor on all assignments Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations Qualifications Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred Minimum 3 years of clinical research experience IBD experience is a must Ability to own issues and problem solve independently Experience in phlebotomy preferred Strong written and verbal communication skils Ability to read, interpret, and apply clinic policies and research protocols Ability to use standard office software Must be able to lift up to 25 pounds At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health. At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.", "summaryDescription" : "Clinical Research Coordinator II at Iterative Health. Skills: Clinical research, Patient recruitment, Protocol adherence. Manage clinical trial activities. Coordinate study visits", "postedDate" : "2026-06-11T22:13:32.073", "createdAt" : "2026-06-11T22:13:32.073", "lastUpdated" : "2026-06-14T23:12:41.882", "ingestTimestamp" : "2026-06-11T22:13:32.073", "mongoId" : "6a2a53f474d8ee00a0600bdd", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 85000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Phlebotomy", "ECG", "Blood draws", "Specimen processing", "Specimen shipping", "Clinical research", "Patient recruitment", "Protocol adherence", "Clinical trials", "Protocol management", "Data entry", "Data integrity", "Data query resolution", "Gastrointestinal", "Hepatology", "Good Clinical Practices", "FDA guidelines", "IATA regulations", "CTMS" ], "skillCount" : 19, "jobCategory" : "other", "jobSubcategory" : "clinical-services", "dataQualityScore" : 0.8888889, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2c5f4c74d8ee00a08eac5b", "title" : "Director, Research - Evaluation & Training", "company" : "Snorkel AI", "industry" : "Technology", "salary" : { "min" : 220000.0, "max" : 330000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director, Research - Evaluation & Training in San Francisco, adjusted for seniority, company size, and the technology industry." }, "location" : "San Francisco", "locations" : [ "San Francisco" ], "timestamp" : "2026-06-14T22:21:08.575", "fingerprint" : "b0792dbc0bd5486acee1ee0ccfe36c6135a2afadd1e1b2e80745bc4080985c7c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/snorkelai/jobs/6020877004", "externalId" : "6020877004", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.7879363,-122.4075201" } ], "locationText" : "San Francisco, California, United States", "experienceLevel" : "Director", "technicalSkills" : "AI, ML", "professionalSkills" : [ "Business judgment", "Market judgment" ], "hardSkillsList" : [ "Evaluation techniques", "Error analysis", "Data valuation" ], "softSkillsList" : [ "Leadership", "Communication", "Storytelling" ], "hardSkills" : [ { "name" : "Evaluation techniques", "level" : "intermediate" }, { "name" : "Error analysis", "level" : "intermediate" }, { "name" : "Data valuation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Communication" }, { "name" : "Storytelling" } ], "majorSkills" : "Data-centric research, Model evaluation, Data valuation", "majorSkillsList" : [ "Data-centric research", "Model evaluation", "Data valuation" ], "coreResponsibilities" : "Own multi-quarter roadmap, Synthesize trends from model-failure analysis, Share trends into recommendations, Quantify how Snorkel data improves model performance, Lead and grow team of researchers, Set high bar for quality, Set high bar for rigor, Set high bar for speed of execution, Act as bridge between findings and Product, Act as bridge between findings and GTM, Act as bridge between findings and customers", "teamCollaboration" : "Bridge findings to Product; Bridge findings to GTM; Bridge findings to customers", "projectManagementSkills" : [ "Roadmap planning" ], "domainKnowledge" : "LLM evaluation; Benchmarking; Model behavior analysis; Data-centric methods", "domainList" : [ "llm-evaluation", "benchmarking", "model-behavior-analysis", "data-centric-methods" ], "domainSpecificKnowledge" : [ "LLM evaluation", "Benchmarking", "Model behavior analysis", "Data-centric methods" ], "communicationSkills" : "Make technical results legible; Make technical results persuasive", "problemSolvingSkills" : "Error analysis; Model failure analysis", "qualificationsBasic" : "7+ years in applied AI, ML, or research, 4+ years managing technical teams, SQL proficiency", "qualificationsPreferred" : "Familiarity with data valuation or data attribution research, Experience working with frontier labs, Experience with public benchmarks, Experience with commercial AI data/eval products", "rawDescription" : "About Snorkel At Snorkel, we believe meaningful AI doesn’t start with the model, it starts with the data. We’re on a mission to help enterprises transform expert knowledge into specialized AI at scale. The AI landscape has gone through incredible changes since 2015, when Snorkel started as a research project in the Stanford AI Lab, to the generative AI breakthroughs of today. But one thing has remained constant: the data you use to build AI is the key to achieving differentiation, high performance, and production-ready systems. We work with some of the world’s largest organizations to empower scientists, engineers, financial experts, product creators, journalists, and more to build custom AI with their data faster than ever before. Excited to help us redefine how AI is built? Apply to be the newest Snorkeler! Snorkel AI came out of the Stanford AI lab and is built on the principle that data development is the core of AI. For years, we have pioneered data-centric methods that power the world’s most sophisticated AI implementations from top enterprises to frontier AI labs. We are looking for a Senior Manager of Research to lead a team focused on data-centric research. About the Role We're looking for a manager to lead a team of researchers to focus on data evaluation, error analysis and data valuation methods to predict model performance. This team is responsible for showcasing the value and quality of Snorkel’s data for model training and evaluation, understanding where today's frontier models fall short, and turning that understanding into a point of view on what benchmarks and datasets these models will benefit from. You and your team will be responsible for Snorkel’s data design flywheel by analyzing model failures, finding capability and skill gaps in current models, suggesting the next benchmarks to invest in and then proving the value of this data for our customers. Main Responsibilities Own a multi-quarter roadmap centered on novel evaluation, error analysis, and data valuation techniques Synthesize and share trends from model-failure analysis and benchmarking into recommendations on the datasets the community should focus on and the ones Snorkel should invest in — making this team a primary input to the company's data strategy. Focus on data valuation techniques that quantify how Snorkel data meaningfully improves model performance Lead and grow a team of researchers, setting a high bar for quality, rigor and speed of execution Act as the primary bridge between the team's findings and Product, GTM, and our customers What We’re Looking For 7+ years in applied AI, ML, or research roles, with 4+ years managing technical teams. A leader who has repeatedly turned research and analysis into business outcomes, and who instinctively connects technical findings to market and customer needs. Strong business and market judgment in the AI/ML space — you understand the competitive and frontier-lab landscape and can prioritize accordingly. Technically conversant and credible: enough depth in LLM evaluation, benchmarking, and model behavior analysis to set direction, judge experimental quality, and pressure-test results — without needing to be the deepest technical expert in the room. A nose for trends: able to look across many evaluation results and failure cases and extract the signal that should drive what gets built next. Excellent communication and storytelling skills, with the ability to make technical results legible and persuasive to non-research audiences. Familiarity with data valuation or data attribution research is a strong plus. Bonus: experience working with frontier labs, public benchmarks, or commercial AI data/eval products. Be Your Best at Snorkel Joining Snorkel AI means becoming part of a company that has market proven solutions, robust funding, and is scaling rapidly—offering a unique combination of stability and the excitement of high growth. As a member of our team, you’ll have meaningful opportunities to shape priorities and initiatives, influence key strategic decisions, and directly impact our ongoing success. Whether you’re looking to deepen your technical expertise, explore leadership opportunities, or learn new skills across multiple functions, you’re fully supported in building your career in an environment designed for growth, learning, and shared success. Snorkel AI is proud to be an Equal Employment Opportunity employer and is committed to building a team that represents a variety of backgrounds, perspectives, and skills. Snorkel AI embraces diversity and provides equal employment opportunities to all employees and applicants for employment. Snorkel AI prohibits discrimination and harassment of any type on the basis of race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local law. All employment is decided on the basis of qualifications, performance, merit, and business need. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.", "summaryDescription" : "Director, Research - Evaluation & Training at Snorkel AI. Skills: Data-centric research, Model evaluation, Data valuation. Own multi-quarter roadmap. Synthesize trends from model-failure analysis", "postedDate" : "2026-06-12T22:26:10.687", "createdAt" : "2026-06-12T22:26:10.687", "lastUpdated" : "2026-06-14T22:21:08.575", "ingestTimestamp" : "2026-06-12T22:26:10.687", "mongoId" : "6a2c5f4c74d8ee00a08eac5b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 220000, "salaryAnnualMax" : 330000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Evaluation techniques", "Error analysis", "Data valuation", "Leadership", "Communication", "Storytelling", "Data-centric research", "Model evaluation", "Business judgment", "Market judgment", "Roadmap planning", "LLM evaluation", "Benchmarking", "Model behavior analysis", "Data-centric methods" ], "skillCount" : 15, "jobCategory" : "other", "jobSubcategory" : "316---research", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology" }, { "id" : "6a2a530b74d8ee00a05fc993", "title" : "Senior/Clinical Research Associate", "company" : "Precision for Medicine", "industry" : "Healthcare", "salary" : { "min" : 7.2E7, "max" : 1.08E8, "currency" : "KRW", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Clinical Research Associate in South Korea, adjusted for the biotech industry and senior experience level." }, "location" : "Remote (South Korea)", "locations" : [ "Remote (South Korea)" ], "timestamp" : "2026-06-14T23:36:21.299", "fingerprint" : "efbdb4e352230c330a42330bb5bb77837af712f5973718a51466f0951dcf0692", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/pfm/jobs/6019361004", "externalId" : "6019361004", "industryFunction" : { }, "structuredLocations" : [ { "country" : "South Korea", "continent" : "as", "workMode" : "remote" } ], "locationText" : "South Korea", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Microsoft Office, EDC CRF", "professionalSkills" : [ "Clinical trial execution", "Scientific knowledge", "Laboratory expertise", "Data sciences", "Study site management", "Audit readiness", "Site start up", "Regulatory documents", "Patient informed consents", "Study budgets", "Investigator contracts", "Informed consent", "Clinical data integrity", "Monitoring reports", "Project documents", "Subject recruitment", "Subject retention", "Investigator site file", "Trial master file", "Essential documents archiving", "Investigational product", "Data review activities", "Data management", "Clinical data quality", "Serious adverse events", "SAE reporting", "Site risks", "Investigator meetings" ], "hardSkillsList" : [ "GCP", "GPP", "ICH-GCP", "Precision SOPs", "Pharmacovigilance issues", "Drug development process", "Regulatory guidance" ], "softSkillsList" : [ "Independent judgment", "Critical thinking", "Interpersonal skills", "Self-motivation", "Team environment" ], "hardSkills" : [ { "name" : "GCP", "level" : "intermediate" }, { "name" : "GPP", "level" : "intermediate" }, { "name" : "ICH-GCP", "level" : "intermediate" }, { "name" : "Precision SOPs", "level" : "intermediate" }, { "name" : "Pharmacovigilance issues", "level" : "intermediate" }, { "name" : "Drug development process", "level" : "intermediate" }, { "name" : "Regulatory guidance", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Independent judgment" }, { "name" : "Critical thinking" }, { "name" : "Interpersonal skills" }, { "name" : "Self-motivation" }, { "name" : "Team environment" } ], "majorSkills" : "Clinical research, Study site management, ICH-GCP", "majorSkillsList" : [ "Clinical research", "Study site management", "ICH-GCP" ], "coreResponsibilities" : "Provide overall support to study sites, Support clinical project teams, Adhere to applicable protocols, Adhere to SOPs, Adhere to guidelines, Adhere to regulatory requirements, Act as point of contact for study sites, Execute core responsibilities consistently, Work independently as study team member, Oversee study site management aspects, Ensure patient safety is protected, Ensure quality of data generated, Provide guidance towards audit readiness, Support preparation for audit, Support required follow-up actions, Update study specific trial management tools, Track study specific trial management tools, Maintain study specific trial management tools, Update status reports, Track status reports, Maintain status reports, Manage site start up procedures, Recruit potential investigators, Prepare EC/IRB submissions, Collect regulatory documents, Review regulatory documents, Review Patient Informed Consents, Adapt Patient Informed Consents, Notify IRB, Notify EC, Notify regulatory authorities, Translate study related documentation, Organize meetings, Assist negotiation of study budgets, Execute investigator contracts, Verify informed consent process, Assess factors affecting subject safety, Assess factors affecting data integrity, Conduct pre-study visits, Conduct qualification visits, Conduct initiation visits, Conduct routine monitoring visits, Conduct close-out visits, Prepare monitoring reports, Submit monitoring reports, Document activities via confirmation letters, Document activities via follow-up letters, Document activities via trip reports, Document activities via communication logs, Document activities via project documents, Support subject recruitment strategies, Support subject retention strategies, Support subject awareness strategies, Enter data into tracking systems, Track all observations, Track ongoing status, Track assigned action items, Resolve assigned action items, Review Investigator Site File, Reconcile Investigator Site File, Reconcile Trial Master File, Ensure investigator site is aware of archiving requirements, Communicate protocol/study issues, Communicate deviations, Implement necessary actions, Develop working relationship with investigators, Develop working relationship with study staff, Serve as ambassador for Precision, Perform investigational product inventory, Perform investigational product reconciliation, Review investigational product storage, Review investigational product security, Verify IP dispensed to subjects, Verify IP administered to subjects, Verify issues associated with blinded information, Verify risks associated with blinded information, Verify issues associated with randomized information, Verify risks associated with randomized information, Apply knowledge to ensure IP labelled, Apply knowledge to ensure IP imported, Apply knowledge to ensure IP released, Apply knowledge to ensure IP returned, Perform data review activities, Review remote EDC CRF, Review patient profiles, Resolve queries, Assist data management personnel, Assist clinical data quality personnel, Resolve data discrepancies, Identify Serious Adverse Events, Process Serious Adverse Events, Identify site risks, Escalate site risks, Suggest contingencies for risks, Own resolution of risks, Prepare for Investigator Meetings, Attend Investigator Meetings, Attend sponsor face-to-face meetings, Participate in global clinical monitoring meetings, Participate in project staff meetings, Attend clinical training sessions, Travel as necessary, Perform other duties as assigned", "teamCollaboration" : "Study sites; Clinical project teams; Site personnel; Precision Project Management; Clinical Trial Management; Site personnel; Project team", "projectManagementSkills" : [ "Clinical Trial Management", "Project Management" ], "domainKnowledge" : "Oncology; Rare Disease; ICH-GCP; GPP; Country regulations; Drug development process", "domainList" : [ "oncology", "rare-disease", "ich-gcp", "gpp", "country-regulations", "drug-development-process" ], "domainSpecificKnowledge" : [ "Oncology", "Rare Disease", "ICH-GCP", "GPP", "Country regulations", "Drug development process" ], "toolProficiency" : [ "Microsoft Office package", "Outlook", "Word", "Excel", "PowerPoint" ], "communicationSkills" : "English communication; Verbal communication; Written communication; Presentation skills", "documentationSkills" : "Regulatory documents; Patient Informed Consents; Study related documentation; Monitoring reports; Confirmation letters; Follow-up letters; Trip reports; Communication logs; Project documents; Investigator Site File; Trial Master File; Essential documents", "problemSolvingSkills" : "Critical thinking; Independent judgment; Problem resolution", "specialRequirements" : "60-70% travel", "outcomesObjectives" : "Consistently low query levels; Acceptable Quality Assurance reports", "qualificationsBasic" : "Bachelor's degree or equivalent, Minimum 2 years on-site monitoring, Fluency in English communication", "qualificationsPreferred" : "1 year oncology experience, Solid experience in clinical research, Ability to work efficiently remotely", "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. Precision for Medicine is looking for a Senior/Clinical Research Associate. Position Summary: The CRA provides overall support to study sites and clinical project teams engaged in clinical research studies. Adheres to applicable protocols, standard operating procedures (SOPs) and all applicable guidelines and regulatory requirements (e.g., International Council for Harmonization (ICH) -Good Clinical Practice (GCP), Good Pharmacoepidemiology Practice (GPP), and country/region-specific regulations). Acts as point of contact for study sites. The CRA is a solid team member who can execute all core responsibilities consistently across several studies using independent judgment and critical thinking. Individual works independently as study team member with minimum support in complex activities. Essentials functions of the job included but not limited to: Oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports. Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions. Updates, tracks and maintains study specific trial management tools/systems, and status reports. If required, manages site start up procedures including the feasibility and recruitment of potential investigators, preparation of EC/IRB submissions, collection and review of regulatory documents, review and adaptation in Patient Informed Consents, notifications to IRB, EC and regulatory authorities, as appropriate, translation of study related documentation, organization of meetings and other tasks as instructed by the Clinical Trial Manager/Project Manager. If required, assists the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee. Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Independently conducts all forms of site visits, including pre-study/ qualification, initiation, routine monitoring, and close-out visits, in accordance with the protocol, local laws, ICH-GCP and Precision SOPs. Prepares and submits for review, accurate and timely monitoring reports from all site visits (on-site and remote). Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs, Clinical Monitoring Plan/Site Management Plan and client requirements. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Communicates effectively and proactively with both site personnel and Precision Project and Clinical Trial Management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues. Develops and maintains good working relationship with investigators and study staff, serving as an ambassador to promote Precision high quality and professional image. Performs investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned. Performs data review activities, including remote EDC CRF and patient profiles review, query resolution, and assists data management and clinical data quality personnel to resolve data discrepancies Identifies and processes Serious Adverse Events according to the procedures defined by the study team. Also demonstrates a full understanding of the SAE reporting process. Identifies site risks and escalates those to Clinical Trial Manager/Project Manager with suggested contingencies. Owns the timely and appropriate resolution of the risk with minimal support from project team. Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. Travels as necessary according to project needs. Performs other duties as assigned by management. Qualifications: Minimum Required: Bachelor's degree / international equivalent or equivalent combination of education and experience ideally in a business, scientific or healthcare discipline. Minimum of 2 years of on-site monitoring experience; 1 year oncology experience preferred Other required: High in proficiency in the Microsoft Office package of programs (Outlook, Word, Excel, and PowerPoint). Customer service demeanour; demonstrate flexibility and teamwork. Ability to focus on detail for extended periods of time, high attention to accuracy. Fluency in English communication, verbally and in writing. Working knowledge of the drug development process. Travelling required (60-70%) Preferred: Solid experience in clinical research or related experience. Excellent organizational skills. Ability to work efficiently in a remote work environment. Competencies: Good knowledge and utilization of ICH-GCP, Precision SOPs, and regulatory guidance. Demonstrates solid interpersonal skills. Exhibits strong self-motivation, is detail-oriented and able to work and plan independently as well as in a team environment. Good written and verbal communication skills and presentation skills. Ability to deliver on commitments. Commitment to performing professionally consistent with Precision Principles. We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company. 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" : "Senior/Clinical Research Associate at Precision for Medicine. Skills: Clinical research, Study site management, ICH-GCP. Provide overall support to study sites. Support clinical project teams", "postedDate" : "2026-06-11T21:25:48.672", "createdAt" : "2026-06-11T21:25:48.672", "lastUpdated" : "2026-06-14T23:36:21.299", "ingestTimestamp" : "2026-06-11T21:25:48.672", "mongoId" : "6a2a530b74d8ee00a05fc993", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "GCP", "GPP", "ICH-GCP", "Precision SOPs", "Pharmacovigilance issues", "Drug development process", "Regulatory guidance", "Independent judgment", "Critical thinking", "Interpersonal skills", "Self-motivation", "Team environment", "Clinical research", "Study site management", "Clinical trial execution", "Scientific knowledge", "Laboratory expertise", "Data sciences", "Audit readiness", "Site start up", "Regulatory documents", "Patient informed consents", "Study budgets", "Investigator contracts", "Informed consent", "Clinical data integrity", "Monitoring reports", "Project documents", "Subject recruitment", "Subject retention", "Investigator site file", "Trial master file", "Essential documents archiving", "Investigational product", "Data review activities", "Data management", "Clinical data quality", "Serious adverse events", "SAE reporting", "Site risks", "Investigator meetings", "Clinical Trial Management", "Project Management", "Oncology", "Rare Disease", "Country regulations", "Microsoft Office package", "Outlook", "Word", "Excel", "PowerPoint" ], "skillCount" : 51, "jobCategory" : "other", "jobSubcategory" : "clinical-solutions", "dataQualityScore" : 0.8888889, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "69dde45b2beec4dd3d9a3f34", "title" : "Clinical Research Associate - Medical Oncology", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 65000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Clinical Research Associate in Duarte, California, adjusted for the healthcare industry and a large company size." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Research", "Hybrid, Days, Days" ], "timestamp" : "2026-06-15T09:11:22.902", "fingerprint" : "6909b7794dda8c6e899322fee53ea064ec21400be4cb7ebbe3ab7aa6c86d6440", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=226305", "externalId" : "226305", "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" : "Associate's Degree", "majorSkills" : "Clinical research, Data analysis, Protocol management", "majorSkillsList" : [ "Clinical research", "Data analysis", "Protocol management" ], "teamCollaboration" : "Institutional teams; PI/supervisor; PI/nurse/supervisor", "projectManagementSkills" : [ "Protocol management" ], "domainKnowledge" : "Clinical research; Oncology; Cancer research; Patient confidentiality", "domainList" : [ "clinical-research", "oncology", "cancer-research", "patient-confidentiality" ], "domainSpecificKnowledge" : [ "Clinical research", "Oncology", "Cancer research", "Patient confidentiality" ], "documentationSkills" : "Protocol documentation; Regulatory documents", "continuousLearning" : "Seminars; Workshops; Professional affiliations", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Join the forefront of groundbreaking research 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. 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. Come join us as a Clinical Research Associate I under which you will manage an assigned set of clinical research studies and protocols to assure efficiency and regulatory compliance. As a successful candidate, you will: Work on data abstraction and analysis. Interface with existing institutional resources/teams, including Posiedon, Honest Broker, STATA, RedCap, Excel, and others. Download and manipulate data from external sources, including National Cancer Database and SEER. Provide project management for computational projects. Assist PI/supervisor with write up of results, and notify them of any roadblocks. Conduct protocol management for an assigned set of clinical studies within the department. Maintain current and accurate protocol documentation. Notify PI/supervisor of pertinent protocol changes and other data management issues or problem areas. Complete and maintain regulatory documents for IRB, DSMB, and PRMC/CPRMC. Compile and submit data on appropriate forms according to protocol. Play active role in recruitment of patients to department studies. Establish and maintain interpersonal relationships with patients, visitors, and other COH personnel, while assuring confidentiality of patient information. Works with PI/nurse/supervisor to schedule protocol-related tests and evaluations. Perform other duties as outlined in the approved protocol. Collect and deliver specimens for analysis, using appropriate materials and procedures specified in the protocol. Ensure proper labeling and obtain pertinent clinical and protocol information on request forms. Develop and maintain knowledge of various aspects of processing specimens, paying particular attention to safety practices and shipping instructions. Maintain professional growth and development through seminars, workshops, and professional affiliations to maintain certification/licensure, and/or keep abreast of latest trends in the field. Ensure work environment is organized and functions efficiently. Attend and participate in meetings as required. Provide staff relief as required to meet the needs of the department. Work with supervisor to ensure appropriate levels of quality are maintained. Your qualifications should include: Associate’s Degree. Experience may substitute for minimum education requirements. One-year experience working in a health care setting, preferably in research. Preferred qualifications: Bachelor’s Degree. Medical Record, Health Information Systems, clinical trials exposure or related health field. 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 Research Associate - Medical Oncology at City of Hope. Skills: Clinical research, Data analysis, Protocol management", "createdAt" : "2026-06-14T07:53:38.069", "lastUpdated" : "2026-06-15T09:11:22.902", "ingestTimestamp" : "2026-06-14T07:53:38.069", "mongoId" : "69dde45b2beec4dd3d9a3f34", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 85000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Clinical research", "Data analysis", "Protocol management", "Oncology", "Cancer research", "Patient confidentiality" ], "skillCount" : 6, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Junior", "dataQualityScore" : 0.6666667, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a53f474d8ee00a0600c0d", "title" : "Senior Clinical Research Coordinator", "company" : "Iterative Health", "industry" : "Healthcare Technology", "salary" : { "min" : 85000.0, "max" : 125000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Clinical Research Coordinator in Dayton, United States, adjusted for seniority and industry." }, "location" : "Dayton, Ohio, United States", "locations" : [ "Dayton", "Ohio", "United States" ], "certifications" : [ "CCRC®", "CCRP®" ], "timestamp" : "2026-06-14T19:57:23.594", "fingerprint" : "c53f5e362d4aa5ca1afb1428f04f6a59a34c990d4746f9c82aadf9b9b9e5fa06", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/iterativehealth/jobs/4686992006", "externalId" : "4686992006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Dayton", "state" : "Ohio", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.7589478,-84.1916069" } ], "locationText" : "Dayton, Ohio, United States", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : 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"Laboratory specimens processing", "level" : "intermediate" }, { "name" : "IATA regulations", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Mentorship" } ], "majorSkills" : "Clinical trials management, Patient care, Regulatory compliance", "majorSkillsList" : [ "Clinical trials management", "Patient care", "Regulatory compliance" ], "coreResponsibilities" : "Manage complex clinical trials, Coordinate study visit schedules, Ensure compliance with study timelines, Ensure compliance with regulatory requirements, Lead patient recruitment initiatives, Lead patient retention initiatives, Support enrollment performance, Support patient engagement, Mentor junior coordinators, Support junior coordinators, Mentor research staff, Support research staff, Conduct protocol-required patient visits, Conduct protocol-required assessments, Perform clinical procedures, Process laboratory specimens, Prepare specimen shipments, Maintain study documentation, Maintain source records, Maintain informed consent forms, Update CTMS, Maintain case report forms, Ensure high-quality data entry, Resolve sponsor data queries, Resolve CRO data queries, Serve as primary point of contact, Build relationships with investigators, Build relationships with referring physicians, Build relationships with sponsors, Build relationships with CRO partners, Prepare for monitoring visits, Support monitoring visits, Prepare for audit visits, Support audit visits, Prepare for inspection visits, Support inspection visits, Review safety reports, Ensure investigator review, Ensure documentation of safety reports, Maintain inventory of study equipment, Maintain oversight of study equipment, Maintain inventory of study supplies, Maintain oversight of study supplies, Maintain inventory of investigational products, Maintain oversight of investigational products, Assess operational challenges, Identify solutions, Recommend process improvements, Enhance site performance, Enhance protocol adherence, Support site performance initiatives, Support enrollment initiatives, Support screen failures initiatives, Support protocol compliance initiatives, Support patient retention initiatives, Contribute to onboarding activities, Contribute to training activities, Contribute to mentorship activities, Support protection of human research participants, Maintain compliance with site SOPs, Maintain compliance with privacy standards, Maintain compliance with research protocols, Perform job related duties", "teamCollaboration" : "Cross-functional collaboration; Work with staff", "projectManagementSkills" : [ "Study start-up", "Study closeout" ], "domainKnowledge" : "Clinical trials; GCP guidelines; HIPAA; Gastrointestinal; Hepatology; Obesity; Cardiology", "domainList" : [ "clinical-trials", "gcp-guidelines", "hipaa", "gastrointestinal", "hepatology", "obesity", "cardiology" ], "domainSpecificKnowledge" : [ "Clinical trials", "GCP guidelines", "HIPAA", "Gastrointestinal", "Hepatology", "Obesity", "Cardiology" ], "toolProficiency" : [ "CTMS", "EDC systems", "Office software" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Study documentation; Source records; Informed consent forms; Case report forms; Safety reports", "problemSolvingSkills" : "Problem-solving", "specialRequirements" : "Sit for extended periods, Stand for extended periods, Move for extended periods, Lift up to 25 pounds", "outcomesObjectives" : "Successful study execution; Enrollment performance; Regulatory compliance; High-quality patient experiences; Patient engagement goals; Site performance; Protocol adherence", "qualificationsBasic" : "5+ years clinical research experience, GCP understanding, FDA regulations understanding, Clinical research operations understanding", "qualificationsPreferred" : "Associate's degree in scientific discipline, Bachelor's degree in scientific discipline, Gastroenterology therapeutic areas experience, Hepatology therapeutic areas experience, Cardiology therapeutic areas experience, CCRC® certification, CCRP® certification, Equivalent clinical research certification", "workSiteFlexibility" : "Onsite", "rawDescription" : "Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide. At Iterative Health, you’ll have the opportunity to help shape the future of clinical research while working alongside a collaborative, mission-driven team. We believe research changes lives, and every team member plays a critical role in improving patient access to innovative therapies. Why This Role Matters As a Senior Clinical Research Coordinator (Sr. CRC) at Iterative Health you will serve as a key team member within the clinical research site, overseeing complex studies while supporting staff development, operational performance, and high-quality patient experiences. This role combines hands-on study coordination with mentorship, process improvement, and cross-functional collaboration to help drive successful study execution, enrollment performance, and regulatory compliance. Where You’ll Drive Impact Lead and independently manage complex industry-sponsored clinical trials from study start-up through closeout Coordinate complex study visit schedules and protocol-related activities while ensuring compliance with study timelines and regulatory requirements Lead patient recruitment and retention initiatives to support enrollment performance and patient engagement goals Mentor and support junior coordinators and research staff on clinical trial processes, patient interactions, sponsor communication, and operational best practices Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations Maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms Ensure high-quality data entry and timely resolution of sponsor and CRO data queries Serve as a primary point of contact for study participants, sponsors, CROs, investigators, and site leadership Build strong relationships with investigators, referring physicians, sponsors, and CRO partners to support study success and patient engagement Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections Review safety reports and ensure timely investigator review and documentation Maintain inventory and oversight of study equipment, supplies, and investigational products onsite Assess operational challenges, identify solutions, and recommend process improvements to enhance site performance and protocol adherence Support site performance initiatives related to enrollment, screen failures, protocol compliance, and patient retention Contribute to onboarding, training, and mentorship activities for new research staff Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies Maintain compliance with all site SOPs, privacy standards, and research protocols Perform job related duties as requested What You Bring to the Team Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline preferred 5+ years of clinical research or healthcare experience Experience in [gastroenterology, hepatology, cardiology] therapeutic areas preferred CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred Strong understanding of GCP, FDA regulations, and clinical research operations Demonstrated ability to independently manage complex clinical trials and competing priorities Experience mentoring or supporting junior research staff Strong written and verbal communication skills Strong organizational skills, attention to detail, and problem-solving capabilities Proficiency with CTMS, EDC systems, and standard office software applications Physical Requirements Ability to sit, stand, and move throughout clinical and office environments for extended periods of time Ability to lift and move up to 25 pounds as needed At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.", "summaryDescription" : "Senior Clinical Research Coordinator at Iterative Health. Skills: Clinical trials management, Patient care, Regulatory compliance. Manage complex 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. A Clinical Research Associate I role is available under Dr Ravi Salgia, a thoracic oncologist. You will support the clinical and translational research program by performing a broad range of research activities. Clinical duties include patient screening and enrollment, informed consent, protocol coordination, and monitoring across oncology clinical trials. You will be responsible for abstracting and managing clinical, pathological, and outcomes data from electronic health records into research databases, ensuring accuracy and regulatory compliance throughout. This role also involves contributing to the preparation and submission of peer-reviewed manuscripts, conference abstracts, and presentations by conducting literature reviews, compiling data, and supporting writing and revision cycles. Additionally, you will assist in the development of research proposals and grant applications for federal and foundation funding mechanisms, including preparation of supporting documents and coordination of timely submissions. This position offers an excellent opportunity for a motivated professional to contribute meaningfully to impactful oncology research while developing expertise across the full spectrum of clinical research operations. As a successful candidate, you will: · Conduct protocol management for an assigned set of multiple research protocols. · Complete and maintain regulatory documents for IRB, DSMB and PRMC/CPRMC · Recruit patients to study and establish and maintain relationships with patients, visitors and other hospital personnel, while assuring confidentiality of patient information · Compile and submit data on appropriate forms according to protocol requirements · Collect and deliver specimens for analysis using specified equipment and ensure proper labeling. Your qualifications should include: · Associates degree. Experience may substitute for minimum education requirements. Bachelors preferred. · One year of experience working in a health care setting, preferably in clinical research · Experience with medical record review, health information systems, and/or clinical trials is preferred · Superb communication and problem-solving skills and able to function independently and proficiently · Demonstrable computer skills in Microsoft Word, Excel, and/or Microsoft Access as well as skills in data management and analyses. 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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baseline for Clinical Research Coordinator II in Tennessee, United States, adjusted for mid-seniority and healthcare industry." }, "location" : "Tennessee, United States", "locations" : [ "Tennessee", "United States" ], "timestamp" : "2026-06-13T22:20:16.260", "fingerprint" : "6c945550b5078930fb3b43c1d5bc1500c469e2d46b0775eab9484656a78d03de", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/careaccess/jobs/4280446009", "externalId" : "4280446009", "industryFunction" : { }, "structuredLocations" : [ { "state" : "Tennessee", "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "Tennessee, United States", "professionalSkills" : [ "Medical terminology", "Research terminology" ], "hardSkillsList" : [ "FDA regulations", "ICH guidelines", "Phlebotomy", "ECGs", "Laboratory results review", "Study medication inventory", "Regulatory documents completion", "Source documents creation", "Informed consent", "Clinical 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"coreResponsibilities" : "Screen study subjects, Enroll study subjects, Monitor clinical research study subjects, Ensure protocol compliance, Ensure regulatory compliance, Coordinate patient activities, Maintain adherence to FDA regulations, Maintain adherence to ICH guidelines, Maintain relationships with study participants, Maintain relationships with Care Access Research personnel, Address patient concerns, Monitor quality, Resolve queries, Interact with patients, Interact with representatives, Interact with investigators, Interact with Care Access Research personnel, Interact with management, Coordinate pre-study site visits, Coordinate site initiation visits, Coordinate monitor visits, Mentor CRC I, Provide onboarding guidance, Provide day-to-day guidance, Identify adverse events, Identify Serious Adverse Events, Notify Principal Investigator, Notify Sponsor, Moderate mixed visit types, Moderate active IP workflows, Moderate AE/SAE workflows, Operate as solo CRC onsite, Prescreen study candidates, Obtain informed consent, Complete visit procedures, Complete basic clinical procedures, Perform blood draws, Record vital signs, Perform ECGs, Review laboratory results, Review ECGs, Review test results, Alert value review, Ensure investigator review, Discuss study medication, Discuss required procedures, Discuss eligibility criteria, Discuss impact on office flow, Record data legibly, Enter data in real time, Record study medication inventory, Record medication dispensation, Record patient compliance, Resolve data management queries, Correct source data, Assist regulatory personnel, Complete regulatory documents, File regulatory documents, Create source documents, Review source documents, Assist with recruitment material planning, Assist with recruitment material creation, Assist in development of recruitment plan, Obtain listing of potential candidates, Call subjects for recruitment, Recruit subjects, Review protocol, Review protocol amendments, Ensure training requirements are met, Ensure study requirements are met, Communicate clearly verbally, Communicate clearly in writing, Anticipate change, Propose change, Manage change, Attend Investigator meetings, Own competing priorities, Prioritize competing priorities, Ensure adequate supplies have arrived", "teamCollaboration" : "Work effectively with diverse team", "domainKnowledge" : "Clinical trials; GCP; FDA regulations; ICH guidelines", "domainList" : [ "clinical-trials", "gcp", "fda-regulations", "ich-guidelines" ], "domainSpecificKnowledge" : [ "Clinical trials", "GCP", "FDA regulations", "ICH guidelines" ], "toolProficiency" : [ "Clinical trials database", "IVR systems", "Electronic data capture", "MS Word", "MS Excel" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Source document creation; Regulatory document completion", "problemSolvingSkills" : "Problem solver; Critical thinker", "specialRequirements" : "Regional commute requirements, Up to 10% travel, Regional travel, Use keyboards, Use computer equipment, Walking, Standing, Sitting, Lifting up to 25lbs, Lifting overhead, Driving", "qualificationsBasic" : "3 years prior Clinical Research Coordinator experience, Recent phlebotomy experience", "qualificationsPreferred" : "Bachelor’s Degree preferred, 1 year of experience as a Care Access Research Clinical Research Coordinator", "workSiteFlexibility" : "Onsite", "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 Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance. How You'll Make An Impact Patient Coordination Prioritize activities with specific regard to protocol timelines  Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.  Maintain effective relationships with study participants and other care Access Research personnel.  Balances protocol needs with patient experience; proactively addresses concerns. Monitors quality metrics; prevents deviations; resolves queries quickly. Interact in a positive, professional manner with patients, .representatives, investigators and Care Access Research personnel and management.  Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.  Mentors CRC I peers; provides onboarding and day‑to‑day guidance. Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)  Moderate complexity; mixed visit types, active IP and AE/SAE workflows. Can operate as solo CRC onsite. Prescreen study candidates   Obtain informed consent per Care Access Research SOP .  Complete visit procedures in accordance with protocol.  Complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.  Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.  Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.  Documentation Record data legibly and enter in real time on paper or e-source documents   Accurately record study medication inventory, medication dispensation, and patient compliance.  Resolve data management queries and correct source data within sponsor provided timelines  Assist regulatory personnel with completion and filing of regulatory documents.  Assist in the creation and review of source documents.  Patient Recruitment Assist with planning and creation of appropriate recruitment materials.  Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database.  Actively work with recruitment team in calling and recruiting subjects   Review and assess protocol (including amendments) for clarity, logistical feasibility Ensure that all training and study requirements are met prior to trial conduct.  Communicate clearly verbally and in writing.  Anticipates needs; proposes solutions; manages change effectively. Attend Investigator meetings as required.   Owns studies; prioritizes competing demands; mentors CRC I. Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)  The Expertise Required Ability to understand and follow institutional SOPs.  Excellent working knowledge of medical and research terminology  Excellent working knowledge of federal regulations, good clinical practices (GCP)  Operates independently for most study activities; escalates complex issues as needed. Ability to communicate and work effectively with a diverse team of professionals.  Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail  Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.  Critical thinker and problem solver  Friendly, outgoing personality; maintain a positive attitude under pressure.  High level of self-motivation and energy  Excellent professional writing and communication skills  Manages stakeholder communications; facilitates visits and meetings. Ability to work independently in a fast-paced environment with minimal supervision.  Certifications/Licenses, Education, and Experience: Bachelor’s Degree preferred, or equivalent combination of education, training and experience.  A minimum of 3 years prior Clinical Research Coordinator experience required  Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator Recent phlebotomy experience required  How We Work Together Location: This is an on-site position with regional commute requirements Travel: This role requires up to 10% travel requirements further explained below. Length of travel will depend upon study requirements, staff needs, and company initiatives. Type of travel required: Regional (within 100 miles) Physical demands associated with this position Include: The ability to use keyboards and other computer equipment. Walking, Standing, Sitting, Lifting (up to 25lbs and overhead), Driving - 20% The expected salary range for this role is $60,000 - $90,000 USD per year for full time team members. Benefits & Perks (US Full Time Employees) Paid Time Off (PTO) and Company Paid Holidays 100% Employer paid medical, dental, and vision insurance plan options Health Savings Account and Flexible Spending Accounts Bi-weekly HSA employer contribution Company paid Short-Term Disability and Long-Term Disability 401(k) Retirement Plan, with Company Match Relocation Support Provided 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 Research Coordinator II at Care Access. Skills: Clinical research, Patient monitoring, Protocol compliance. Screen study subjects. 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Collaborate with health care team; Assist with primary CRC III", "projectManagementSkills" : [ "Clinical trials management" ], "domainKnowledge" : "Drug Development Program; Cancer Clinical Research; ICH/GCP guidelines; Oncology; Clinical research protocols; Laboratory procedures; IATA shipping regulations", "domainList" : [ "drug-development-program", "cancer-clinical-research", "ich-gcp-guidelines", "oncology", "clinical-research-protocols", "laboratory-procedures", "iata-shipping-regulations" ], "domainSpecificKnowledge" : [ "Drug Development Program", "Cancer Clinical Research", "ICH/GCP guidelines", "Oncology", "Clinical research protocols", "Laboratory procedures", "IATA shipping regulations" ], "toolProficiency" : [ "MS Office", "MS Word", "MS Excel" ], "communicationSkills" : "Verbal communication; Written communication; Patient teaching; Family teaching", "documentationSkills" : "Source documentation", "continuousLearning" : "Work towards certification", "problemSolvingSkills" : "Analytical; Problem solving; Clinical critical thinking", "specialRequirements" : "Occasional Saturdays", "qualificationsBasic" : "Bachelor's degree required, Current certificate of competence required, Registered Nurse required, 3 years experience required, Excellent phlebotomy skills, Excellent IV skills, Excellent CVL skills, Nursing process utilization, Good physical assessment skill, Good psychosocial assessment skill, Good patient/family teaching skill, Autonomous clinical critical thinking, Analytical skills, Problem solving skills, Excellent interpersonal skills, Excellent verbal skills, Excellent written skills, Ability to set priorities, Work independently with accuracy, 3 years clinical experience oncology", "qualificationsPreferred" : "CNA certification in Oncology, DeSouza Chemoio certification, Clinical research certification, IATA shipping regulations knowledge, Basic laboratory procedures knowledge, Previous clinical research experience, Training in ICH/GCP guidelines, MS Office proficiency desired, MS Word proficiency desired, MS Excel proficiency desired", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "UHN is Canada’s #1 hospital and the world’s #1 publicly funded hospital. With 10 sites and more than 44,000 TeamUHN members, UHN consists of Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute, The Michener Institute of Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care. UHN has the largest hospital-based research program in Canada, with major research in neurosciences, cardiology, transplantation, oncology, surgical innovation, infectious diseases, genomic medicine and rehabilitation medicine. UHN is a research hospital affiliated with the University of Toronto. UHN’s vision is to build A Healthier World and it’s only because of the talented and dedicated people who work here that we are continually bringing that vision closer to reality. [www.uhn.ca](https://www.uhn.ca/) Union: Non-Union Number of Vacancies: 1 New or Replacement Position: Replacement Site: Princess Margaret Cancer Centre Department: Cancer Clinical Research Unit (CCRU) Nursing Reports to: Clinical Research Nurse Manager Salary Range: $84,779 - $105,968 per year Hours: 37.5 Hours Per Week Shifts: Monday to Friday, and occasional Saturdays Status: Permanent Full-time Closing Date: July 3, 2026 Position Summary: The Clinical Research Coordinator collaborates with Investigators and health care team to assume responsibility for the overall patient management and coordination of several clinical studies for the Drug Development Program at Princess Margaret Cancer Centre. Studies include pharma-sponsored, cooperative group sponsored (such as NCIC) as well as Investigator initiated trials. Duties: * Coordination of patient activities such as sample collection including processing and shipment of samples according to clinical trials protocols * Assessments, vital signs, ECG’s, monitoring and administration of treatments as per study protocol * Assists the primary Clinical Research Coordinator III with clinical care for patients participating in clinical trials and the implementation and coordination of all aspects of data collection and source documentation, as per UHN policy and ICH/GCP guidelines ## Qualifications * Bachelor’s degree, or recognized equivalent, and current certificate of competence (licensure/registration) from a college legislated under the Regulated Health Professions Act, required * Registered Nurse with a minimum of 3 (three) years experience. * Excellent phlebotomy, IV and CVL skills * CNA certification in Oncology preferred * deSouza Chemo/Bio certification preferred * Excellent organizational and time management skills required * Demonstrated knowledge and ability to utilize the nursing process in planning, implementing and evaluating patient care * Evidence of good physical assessment, psychosocial assessment and patient/family teaching skill * Autonomous clinical critical thinking ability * Recognized certification in clinical research (ACRP or SOCRA) obtained or plans to work towards. * Knowledge of IATA shipping regulations and basic laboratory procedures an asset * Minimum one (3) year clinical experience in oncology with strong knowledge base * Previous clinical research experience preferred * Training in ICH/GCP guidelines an asset. * Strong analytical and problem solving skills * Excellent interpersonal, verbal and written communication skills required * Ability to set priorities and work independently with accuracy in a dynamic environment * Proficiency with MS Office software - Word and Excel desired. ## Additional Information Why join UHN? In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of benefits, programs and perks. It is the comprehensiveness of these offerings that makes it a differentiating factor, allowing you to find value where it matters most to you, now and throughout your career at UHN. * Competitive offer packages * Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP ) * Close access to Transit and UHN shuttle service * A flexible work environment * Opportunities for development and promotions within a large organization * Additional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on-site gyms, etc.) Current UHN employees must have successfully completed their probationary period, have a good employee record along with satisfactory attendance in accordance with UHN's attendance management program, to be eligible for consideration. All applications must be submitted before the posting close date. UHN uses email to communicate with selected candidates. Please ensure you check your email regularly. Please be advised that a Criminal Record Check may be required of the successful candidate. Should it be determined that any information provided by a candidate be misleading, inaccurate or incorrect, UHN reserves the right to discontinue with the consideration of their application. UHN is an equal opportunity employer committed to an inclusive recruitment process and workplace. Requests for accommodation can be made at any stage of the recruitment process. Applicants need to make their requirements known. We thank all applicants for their interest, however, only those selected for further consideration will be contacted.", "summaryDescription" : "Clinical Research Coordinator III (PK) at University Health Network. Skills: Patient management, Clinical studies coordination, Data collection, Oncology clinical research. Coordinate patient activities. 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MEADOWS ELEMENTARY SCHOOL (110)
12037 PENDER LANE
MEADOWS PLACE, 77477

" ], "timestamp" : "2026-06-16T02:08:17.344", "fingerprint" : "dbe14311d67a36cb321c918184ab4b2975657cf6ff0163be8a26cbfe7ae9fd3a", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa210.taleo.net/careersection/ex/jobdetail.ftl?job=191913", "externalId" : "191913", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Meadows Place", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "29.6513439,-95.5880005" } ], "locationText" : "Meadows Place, Texas, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Instructional strategies", "Lesson planning", "Student behavior management", "Progress monitoring", "Data evaluation", "Instructional techniques", "Evidence based strategies" ], "hardSkillsList" : [ "Early childhood education", "Progress documentation", "Student assessment", "Instructional planning", "Behavioral intervention", "Housekeeping tasks", "Cultural responsiveness", "Trauma-informed practices" ], "hardSkills" : [ { "name" : "Early childhood education", "level" : "intermediate" }, { "name" : "Progress documentation", "level" : "intermediate" }, { "name" : "Student assessment", "level" : "intermediate" }, { "name" : "Instructional planning", "level" : "intermediate" }, { "name" : "Behavioral intervention", "level" : "intermediate" }, { "name" : "Housekeeping tasks", "level" : "intermediate" }, { "name" : "Cultural responsiveness", "level" : "intermediate" }, { "name" : "Trauma-informed practices", "level" : "intermediate" } ], "majorSkills" : "Early childhood development, Instructional delivery, Student assessment, Collaboration", "majorSkillsList" : [ "Early childhood development", "Instructional delivery", "Student assessment", "Collaboration" ], "coreResponsibilities" : "Co-plan instructional strategies, Implement instructional activities, Cater to diverse learning styles, Accommodate developmental levels, Use age-appropriate materials, Use technology to enhance learning, Co-develop lesson plans, Develop daily routines, Incorporate playful learning experiences, Assess student abilities, Maintain documentation, Evaluate student achievement, Track student development, Use data to evaluate achievement, Manage learner behaviors, Ensure conducive learning environment, Supervise students, Manage student behavior, Intervene to control disruptive behavior, Report disruptive behavior, Manage allotted learning time, Delegate responsibilities, Provide for basic student needs, Perform housekeeping tasks, Sanitize student work areas, Sanitize instructional materials, Maintain clean learning environment, Support school-wide student activities, Participate in social events, Participate in fund-raising, Employ instructional techniques, Use research to meet student needs, Collaborate with BakerRipley staff, Deliver Pre-K 3 Head Start expectations, Maintain professional communication with families, Inform families of student progress, Engage families in instructional expectations, Coordinate with professional staff, Maximize learning opportunities, Implement daily lessons, Work in various capacities, Seek assistance from resource personnel, Participate in professional development activities, Attend continuing education courses, Implement evidence based strategies, Receive coaching support", "teamCollaboration" : "Head Start Co-Teacher; BakerRipley staff; Other professionals; Instructional assistants; Parents", "domainKnowledge" : "Early childhood growth; Early childhood development; Head Start program", "domainList" : [ "early-childhood-growth", "early-childhood-development", "head-start-program" ], "domainSpecificKnowledge" : [ "Early childhood growth", "Early childhood development", "Head Start program" ], "toolProficiency" : [ "CIRCLE" ], "communicationSkills" : "Written communication; Oral communication", "documentationSkills" : "Student progress documentation; Student achievement documentation", "continuousLearning" : "Professional development activities; Continuing education courses", "specialRequirements" : "Occasional walking, Occasional standing, Occasional sitting, Occasional bending, Occasional stooping, Occasional kneeling, Occasional crouching, Occasional crawling, Lifting less than 40 pounds, Use hands to finger, Handle objects, Feel objects, Use tools, Reach with hands, Talk or hear, Close vision, Color vision, Adjust focus, Attendance at conferences, Attendance at professional development, Normal safety precautions, Prolonged hours, Irregular hours, Emotional control under stress, Travel to various campuses, Travel to district meeting sites, Travel to conferences, Travel out of state, Work after reporting hours, Work weekends, Exposure to bodily fluids, Exposure to childhood illnesses, Frequent interruptions, Engagement with families, Engagement with public", "outcomesObjectives" : "Meet educational goals; Meet reporting requirements", "qualificationsBasic" : "Bachelor's degree in education, Excellent communication skills in English, Good knowledge of FBISD program, Good knowledge of content, curriculum, methods, materials, and equipment, Good knowledge of early childhood growth and development", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Job Overview The Pre-K 3 Collaboration Teacher plays a key role in the partnership between Fort Bend ISD and BakerRipley Head Start, delivering instruction and educational support to three- and four-year-old students at collaboration campuses. In partnership with the Head Start Co-Teacher, this role involves planning lessons, managing student behavior, assessing progress, and adapting instruction to meet individual needs. The teacher will use resources from both FBISD and Head Start to support eligible children and their families. Ongoing, professional collaboration with the BakerRipley Co-Teacher is essential. Both educators are equal partners in creating a cohesive, inclusive, and supportive learning environment. These responsibilities highlight a collaborative partnership between the Pre-K 3 collaboration teacher and Head Start co-teacher, ensuring a comprehensive and cohesive educational experience for young children. This partnership addresses student's intellectual, social, and physical development while adhering to regulatory standards and fostering an engaging learning environment. Position Description Essential Duties and Responsibilities Instruction/Planning Co-plan and implement instructional strategies and activities that cater to and accommodate diverse learning styles and cognitive and physical developmental levels, using a variety of age-appropriate instructional materials and technology to enhance learning; Co-develop lesson plans and daily routines informed by observations and documentation of children's interests and current levels of functioning; Co-implement instructional programs that incorporate purposeful and developmentally appropriate playful learning experiences, considering different learning styles and a range of learning curves; Co-assess student abilities, maintain documentation, and continually evaluate student achievement to meet educational goals and reporting requirements; Use CIRCLE and other district-provided progress monitoring tools to track student development and whole group and individualized instruction; Maintain documentation of student progress and use data to continually evaluate achievement and meet reporting requirements. Student Support/ Supervision Manage learner behaviors within an instructional setting to ensure the environment is conducive to the learning process; Supervise students and manage student behavior during instructional and non-instructional periods throughout the school or center and intervene to control and modify disruptive behavior, reporting to the appropriate administrator as appropriate; Manage allotted learning time to maximize student achievement; May delegate responsibilities to instructional assistants, parents, and student volunteers; Provide for the basic needs of students unable to care for themselves including, but not limited to toilet training and support with self-feeding; Perform housekeeping tasks, such as sanitizing student work areas and instructional materials in order to maintain a clean and orderly learning environment; Support or participate in school-wide student activities, social events and approved fund-raising activities; Employ a variety of instructional techniques and media based on performance-based assessment and research to meet the needs of individual students or groups. Collaboration and Coordination Collaborate with BakerRipley staff and other professionals to deliver Pre-K 3 Head Start instructional expectations and related activities; Maintain consistent, professional communication with families, both written and oral to inform them of student(s) progress; Engage families in understanding and supporting instructional expectations during parent meetings and weekly communication and other settings such as online conferences and school events; Coordinate with other professional staff to maximize learning opportunities and implement daily lesson plans; Work in various capacities (self-contained, team, departmental, itinerant, or fieldwork site) and seek assistance from resource personnel as needed. Professional Development Participate in all required/assigned FBISD and BakerRipley Head Start in-service/professional development activities and/ or staff meetings; Attend all required continuing education courses, and implement evidence based strategies with in class coaching support from an instructional coach, and/or assigned FBISD/BakerRipley Head Start staff. Supervisory Responsibilities None Qualification Requirements To perform this job successfully, an individual must be able to perform each of the above essential duties satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or abilities, required unless otherwise stated as preferred. Reasonable accommodations may be made to enable individuals with disabilities to perform the essentials functions. Bachelor's degree in education, required. Master's degree degree in early childhood education or early childhood special education, preferred. Valid Teaching Certification Issued by Texas Education Agency appropriate to subject and grade level of assignment Early Childhood Teaching Certification (Gen. Ed or Bilingual) in addition to one of the 7 options listed in this job description is required to teach prekindergarten in FBISD, per high-quality PreK components per TEC §29.167 (b) and 19 TAC §102.1003 (d), and §102.1003 (f) (4) Valid Bilingual Certification is needed for for the Bilingual program. Valid Texas ESL Certification is needed for English/ESL program. Texas Food Handler's Certificate obtained within 30 days of hire. Minimum of 3 years Early Childhood Ability to establish and maintain effective relationships; Ability to collect and analyze data for instruction and program evaluation purposes; Excellent communication skills, both orally and in writing, in English and Spanish; Good knowledge of the FBISD program of students related to assignments and public-school mission, goals, and organization; Good knowledge of content, curriculum, methods, materials, and equipment of instructional specialty(ies) to which assigned; Good knowledge of early childhood growth and development. Physical Requirements/Working Conditions The work environment characteristics and physical demands described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Work is performed in classrooms, offices, work stations and meeting rooms. The position requires occasional walking, standing, sitting, bending, stooping, kneeling, crouching, crawling, and lifting/carrying work related items weighing less than 40 pounds, such as books, papers and presentation materials. The employee is regularly required to use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; and talk or hear. Specific vision abilities required by this job include close vision, color vision, and the ability to adjust focus. Attendance at conferences and professional development is required. Work involves everyday risks and discomforts which require normal safety precautions when operating equipment or performing job duties. May work prolonged or irregular hours and must be able to maintain emotional control under stress. Additional Information This position may require travel to various campuses, district meeting sites and conferences/meetings in and out of state. This position may require work after normal reporting hours and weekends. Exposure to bodily fluids and frequent childhood, pre-teen, or teen illnesses may occur. Frequent interruptions and engagement with families and the public are part of the role. Cultural responsiveness and trauma-informed practices are highly valued in this position. TEXAS-MEADOWS PLACE", "summaryDescription" : "Teacher Pre-K-3 Collaboration at Fort Bend ISD. Skills: Early childhood development, Instructional delivery, Student assessment, Collaboration. Co-plan instructional strategies. Implement instructional activities", "createdAt" : "2026-06-14T18:50:52.589", "lastUpdated" : "2026-06-16T02:08:17.344", "ingestTimestamp" : "2026-06-14T18:50:52.589", "mongoId" : "6a1614ed58b93c861e8d877e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 52000, "salaryAnnualMax" : 75000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Early childhood education", "Progress documentation", "Student assessment", "Instructional planning", "Behavioral intervention", "Housekeeping tasks", "Cultural responsiveness", "Trauma-informed practices", "Early childhood development", "Instructional delivery", "Collaboration", "Instructional strategies", "Lesson planning", "Student behavior management", "Progress monitoring", "Data evaluation", "Instructional techniques", "Evidence based strategies", "Early childhood growth", "Head Start program", "CIRCLE" ], "skillCount" : 21, "jobCategory" : "education", "jobSubcategory" : "support", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Education", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2abb3074d8ee00a06e89db", "title" : "Senior Clinical Research Associate", "company" : "Ergomed", "industry" : "Pharmaceuticals", "salary" : { "min" : 135000.0, "max" : 175000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Clinical Research Associate in San Francisco, adjusted for industry and company size." }, "location" : "San Fransisco, California, United States", "locations" : [ "San Fransisco", "California", "United States" ], "timestamp" : "2026-06-14T23:15:07.893", "fingerprint" : "2cb063b00d761d58752d125fe8ac64ca4ae318499bfc70c8b9b7fcc9ff01aae9", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/Ergomed/744000131599447-senior-clinical-research-associate-california-", "externalId" : "744000131599447", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.7879363,-122.4075201" } ], "locationText" : "San Francisco, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "College/University degree", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Life Sciences", "Clinical study conduct" ], "hardSkillsList" : [ "Oncology", "Rare Disease" ], "softSkillsList" : [ "Problem-solving" ], "hardSkills" : [ { "name" : "Oncology", "level" : "intermediate" }, { "name" : "Rare Disease", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Problem-solving" } ], "majorSkills" : "Clinical Research, Oncology, Rare Disease", "majorSkillsList" : [ "Clinical Research", "Oncology", "Rare Disease" ], "coreResponsibilities" : "Perform monitoring visit activities, Identify investigators, Verify investigator qualifications, Train investigational site staff, Support regulatory submissions, Support EC submissions, Participate in mentoring new staff, Perform co-monitoring visits", "teamCollaboration" : "Dynamic team environment", "domainKnowledge" : "Oncology; Rare Disease", "domainList" : [ "oncology", "rare-disease" ], "domainSpecificKnowledge" : [ "Oncology", "Rare Disease" ], "documentationSkills" : "Clinical documentation", "continuousLearning" : "Training and career development opportunities; Personal and professional growth", "problemSolvingSkills" : "Problem-solving", "specialRequirements" : "Travel nationally", "outcomesObjectives" : "Make a positive impact in patient’s lives", "qualificationsBasic" : "College/University degree, Extensive on-site monitoring experience, Full working proficiency in English", "qualificationsPreferred" : "Experience in phase 2/3 trials, Experience of complex trials in oncology or rare disease", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you have a voice!) creative contribution and realistic career development. We have nourished a true international culture here at Ergomed. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. Come and join us in this exciting journey to make a positive impact in patient’s lives. * Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study * Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period. * Trains investigational site staff as necessary * When applicable, supports preparation of regulatory and / or EC submissions * Participates in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance. ## Qualifications * College/University degree in Life Sciences or an equivalent combination of education, training & experience * Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials in oncology or rare disease * Full working proficiency in English * Ability to plan, multitask and work in a dynamic team environment * Communication, collaboration, and problem-solving skills * Ability to travel nationally ## Additional Information We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. We offer: * Training and career development opportunities internally * Strong emphasis on personal and professional growth * Friendly, supportive working environment * Opportunity to work with colleagues based all over the world, with English as the company language Our core values are key to how we operate, and if you feel they resonate with you then Ergomed is a great company to join! Quality Integrity & Trust Drive & Passion Agility & Responsiveness Belonging Collaborative Partnerships We look forward to welcoming your application.", "summaryDescription" : "Senior Clinical Research Associate at Ergomed. Skills: Clinical Research, Oncology, Rare Disease. Perform monitoring visit activities. Identify investigators", "postedDate" : "2026-06-11T07:02:51.000", "createdAt" : "2026-06-12T01:53:38.581", "lastUpdated" : "2026-06-14T23:15:07.893", "ingestTimestamp" : "2026-06-12T01:53:38.581", "mongoId" : "6a2abb3074d8ee00a06e89db", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 135000, "salaryAnnualMax" : 175000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Oncology", "Rare Disease", "Problem-solving", "Clinical Research", "Life Sciences", "Clinical study conduct" ], "skillCount" : 6, "jobCategory" : "research", "jobSubcategory" : "Clinical Monitoring", "dataQualityScore" : 1.0, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" } ], "status" : 200, "message" : "evaluate potential external clinical research collaboration opportunities jobs", "metadata" : { "title" : "evaluate potential external clinical research collaboration opportunities" }, "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 16282, "totalPages" : 326, "hasNext" : true, "hasPrevious" : false } }

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