{ "count" : 58079, "data" : [ { "id" : "6a308763f292fd229c0887a4", "title" : "Clinical Trial Manager / Associate Clinical Trial Manager", "company" : "ClinChoice", "salary" : { "min" : 95000.0, "max" : 145000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Clinical Trial Manager in the United States, adjusted for mid-seniority and the biotech industry." }, "location" : "United States ", "locations" : [ "United States" ], "timestamp" : "2026-06-16T12:20:07.242", "fingerprint" : "3fb43a822fe7bf18678448f6e62bbd872c977735382e496f4e72ffdfbb159e29", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/clinchoice/jobs/4898549101", "externalId" : "4898549101", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "hybrid" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceLevel" : "Manager", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "ClinChoice is seeking a Clinical Trial Manager / Associate Clinical Trial Manager to join one of our sponsor partners, a Boston-based biotech company focused on CNS disorders. This is a direct-hire, hybrid position requiring three days per week in the office. In this role, you will partner closely with Clinical Operations leadership to support the planning and execution of global clinical trials across multiple indications. It is a highly visible, hands-on opportunity with significant impact on study delivery and operational success. The ideal candidate will have 5+ years of clinical operations experience in biotech or pharma, with a strong background managing outsourced global Phase I–III clinical trials and supporting study start-up activities. They will be highly organized, collaborative professional with expertise in CRO/vendor oversight, trial execution, GCP compliance, and cross-functional coordination to support the successful delivery of a global Phase III study. ClinChoice is a global full-service CRO with a strong focus on quality and professional development. As a client-facing role, we are looking for confident candidates with the ability to work independently while establishing a high-trust environment with their client counterparts. Main Job Tasks and Responsibilities: Provide support to the Clinical Operations Lead (COL) in the planning, execution, and oversight of a global phase 3 clinical trial from study start-up to close-out. Support the development, review and tracking of study-related documents (protocols, ICFs, investigative brochure, monitoring visit reports, etc.) with cross functional team collaboration. Support start-up activities to help accelerate country and site activations. Oversee CRO and vendors, monitor performance metrics, and ensure timely and high-quality deliverables. Track study timelines, enrollment, protocol deviations, data trends, and sample management in partnership with CRO and internal stakeholders. Maintain and organize trial documentation (e.g., TMF/eTMF oversight, trackers, meeting minutes) ensuring that study documentation is in a continuous state of inspection readiness. Contribute to inspection readiness activities and ensure compliance with GCP and SOPs. Help identify and resolve site risks and/or issues to foster positive site relationships. Coordinate internal team meetings and participate in cross-functional study meetings. Proactively communicate study updates with key internal and external stakeholders. Education, Experience and Skills: The Application Process Bachelor’s degree is preferably in life sciences or healthcare related field. 5+ years of clinical operations experience within the biotech or pharma industry required Experience managing outsourced global clinical trials across Phase I–III. Prior involvement in study start-up activities strongly preferred Solid understanding of GCP, ICH guidelines, and the clinical development process. Experience with clinical trial management systems (CTMS), eTMF, and other operational tools. Ability to multitask and flex across projects as priorities and deadlines shift. Highly organized with excellent communication and interpersonal skills. Strong attention to detail and ability to multitask in a dynamic, fast-paced setting. A collaborative team player that takes initiative. Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical devices, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key Words: Clinical Trial Manager, Associate Clinical Trial Manager, Clinical Trial Management, Global, Clinical Study Management, Clinical Trials, Phase III Studies, CRO Oversight, Study Start-Up, Vendor Management, TMF, GCP/ICH Compliance, eTMF/CTMS, Clinical Operations, Site Activation, Inspection Readiness, Risk Management, Cross-Functional Collaboration, Protocol Deviations, Enrollment Management, Biotech/Pharma, CNS, Trial Execution. #LI-VH #LI-Hybrid #Clinical Trial Manager # Permanent", "summaryDescription" : "Clinical Trial Manager / Associate Clinical Trial Manager at ClinChoice", "postedDate" : "2026-06-16T01:21:02.433", "createdAt" : "2026-06-16T01:21:02.433", "lastUpdated" : "2026-06-16T12:20:07.242", "ingestTimestamp" : "2026-06-16T01:21:02.433", "mongoId" : "6a308763f292fd229c0887a4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 145000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 971.4454, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a306bbbf292fd229cfd1899", "title" : "Alternance - Assistant / Assistante administratif", "company" : "Artelia", "industry" : "Mechanical Or Industrial Engineering", "salary" : { "min" : 10000.0, "max" : 12000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level administrative assistant in Melun, France, adjusted for the engineering industry and full-time employment." }, "location" : "Melun, IDF, France", "locations" : [ "Melun", "IDF", "France" ], "timestamp" : "2026-06-16T13:06:02.764", "fingerprint" : "93e1db4365a0e94f88896975863cf9fc4cb861ec50d0a2d3dbff0654ba2af093", "source" : "smartrecruiters", "language" : "fr", "applyUrl" : "https://jobs.smartrecruiters.com/Artelia/744000132143160-alternance-assistant-assistante-administratif-", "externalId" : "744000132143160", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Melun", "state" : "Ile-de-France", "country" : "France", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "48.5399270,2.6608169" } ], "locationText" : "Melun, Ile-de-France, France", "employmentType" : "FULL_TIME", "experienceLevel" : "not-applicable", "professionalSkills" : [ "Analyse", "Synthèse" ], "coreResponsibilities" : "Enregistrer les commandes, Gérer les accusés réception, Traiter les factures, Effectuer les relances clients, Consulter les fournisseurs, Rédiger les commandes, Relancer les fournisseurs, Gérer les litiges fournisseurs, Pointer les éléments mensuels, Préparer les éléments de paie, Contrôler les notes de frais, Suivre les absences, Suivre les déplacements, Suivre le mouvement du personnel, Gérer les courriers, Suivre les véhicules, Suivre le parc informatique, Suivre les formations professionnelles, Gérer la documentation projet, Gérer le secrétariat QSSE", "domainKnowledge" : "Ingénierie bâtiment; 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Nous sommes un groupe d'ingénierie , acteur majeur dans les domaines du bâtiment , de l’eau , de l’énergie , de l’industrie et de la mobilité. Détenu à 100% par nos salariés , nous sommes unis par une même passion, celle d’exercer un métier qui allie l’art de concevoir avec ingéniosité et de réaliser avec engagement. Nos 11 000 collaborateurs et collaboratrices , dans plus de 40 pays , créent chaque jour des solutions pour une vie positive au travers de nos enjeux stratégiques pour la planète et l’humanité. Nos équipes sont à taille humaine, privilégiant la proximité, les échanges quotidiens et le partage d’expérience. Dans le cadre de ce poste, vous rejoignez ARTELIA INDUSTRIE, composé de 850 collaborateurs passionnés, répartis sur plus de 30 implantations en France, Belgique, Suisse et Maroc. Ensemble, nous concevons, adaptons et modernisons les installations industrielles pour répondre aux défis de demain : production, performance économique, transition énergétique et sécurité des installations. * Un savoir-faire reconnu : Nous excellons dans la mise en œuvre des différents procédés de production en nous appuyant sur nos expertises pointues en équipements, tuyauteries, mécanique, électricité, instrumentation, automatisme, structures métalliques, génie civil et bâtiment. * Une activité diverse avec des projets d’envergure et des projets de proximité : Nos équipes interviennent sur des secteurs stratégiques tels que le Raffinage et recyclage carbone, la Pétrochimie, la Chimie, la Pharmacie, le Nucléaire, le Gaz, l’Offshore, l’Aéronautique, le Ferroviaire, la Construction navale et spatiale, la Sidérurgie, les Mines, la Microélectronique et la Défense. Pour faciliter la lecture, l’écriture inclusive n’est pas utilisée dans le corps de cette annonce, les termes employés au masculin se réfèrent aussi bien aux femmes, hommes qu'aux personnes non binaires. Vos missions Votre tuteur accompagnera votre progression sur les missions suivantes : * L’administration clients/ fournisseurs : * Enregistrement des commandes, accusé réception, factures, relances clients … * Consultation fournisseurs, rédaction des commandes, relance, factures et litiges fournisseurs… * La gestion du personnel : pointage mensuels, préparation des éléments de paie, contrôle des notes de frais, suivi des absences, des déplacements, le suivi du mouvement du personnel, … * Le suivi administratif : courriers, suivi des véhicules, suivi du parc informatique, suivi des formations professionnelles, … * Le secrétariat technique : Gestion documentaire sur Projet et secrétariat QSSE sur plateforme interne Votre équipe En intégrant l’établissement de Saint-Ouen (93), vous rejoignez une équipe dynamique et ambitieuse, où chaque projet est une opportunité de monter en compétences et d’évoluer dans un environnement stimulant. ## Qualifications Vos atouts Vous êtes le candidat idéal / la candidate idéale si vous préparez une formation Bac+2 à Bac+3 type BTS/DUT Gestion de la PME ou Licence/Bachelor en gestion ou équivalent. Vous êtes une personne rigoureuse, méthodique avec une bonne capacité d’analyse et de synthèse. Vous aimez le travail en équipe et savez facilement vous intégrer à un groupe. Vous maitrisez les outils informatiques tels que le pack office La maîtrise de l’anglais est un plus ## Additional Information Nous vous offrons : * Un tremplin pour votre future carrière chez Artelia * Un tuteur proche de vous au sein d'une équipe à taille humaine * Des experts métiers pour vous accompagner * Une montée en compétences en travaillant sur des projets variés, de différentes tailles, y compris sur des projets emblématiques * Une entreprise sociale et citoyenne : accords diversité & inclusion, protection sociale et couverture mutuelle de qualité, un engagement via la Fondation Artelia * Une politique de partage des résultats : intéressement et participation, nombreux avantages et réductions pour les activités via les œuvres sociales, forfait mobilité durable... * Une équipe RH dédiée pour vous guider durant votre alternance Notre process de recrutement : Mieux se connaître pour se choisir, c’est ce que nous vous proposons lors des 2 étapes de notre processus de recrutement : 1. Echange téléphonique / Entretien avec un recruteur pour mieux cerner vos attentes et orienter votre candidature. L’objectif est de vous présenter notre groupe, les perspectives de carrière, les contours du poste envisagé, et surtout comprendre qui vous êtes, vos aspirations, vos motivations, votre projet professionnel 2. Entretien avec un manager opérationnel : il vous présentera plus en détail les missions, ce qu’il attend de vous, le mode de fonctionnement de l’équipe, les projets. #LI-SR1", "summaryDescription" : "Alternance - Assistant / Assistante administratif at Artelia. Enregistrer les commandes. 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Architecture teams; R&D leadership; Executive stakeholders; International stakeholders", "projectManagementSkills" : [ "Roadmap development", "Portfolio decisions" ], "domainKnowledge" : "Healthcare solutions; Clinical portfolio; Health IT; Regulated environments; AI in healthcare", "domainList" : [ "healthcare-solutions", "clinical-portfolio", "health-it", "regulated-environments", "ai-in-healthcare" ], "domainSpecificKnowledge" : [ "Healthcare solutions", "Clinical portfolio", "Health IT", "Regulated environments", "AI in healthcare" ], "communicationSkills" : "Executive presence; Simplify technical issues; Influence strategic decisions", "documentationSkills" : "Documentation creation; Cross-training documentation", "continuousLearning" : "Continuous learning culture; Dedicated training time; Skill development platform; Access to tools", "innovationCreativity" : "Explore and innovate; Next generation solutions", "problemSolvingSkills" : "Root cause analysis; Troubleshooting; Risk assessment", "outcomesObjectives" : "Improve delivery predictability; Improve execution performance; Achieve measurable productivity gains; Reduce production incidents; Reduce customer defects; High team engagement; Organizational resilience", "qualificationsBasic" : "15+ years progressive software engineering, Management of managers experience, Multi-product environments experience, Improve delivery performance at scale, Improve production stability at scale, Improve organizational productivity at scale, Full command of French, Full command of English", "qualificationsPreferred" : "Health IT experience, Regulated environments experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Depuis plus de 40 ans, LGI développe des solutions logicielles en santé. Aujourd'hui, l'IA est au cœur de notre façon de développer et s'intègre dans la prochaine génération de nos solutions — pas une finalité, mais le levier pour contribuer à la mission qui nous anime : améliorer la performance des établissements de soins de santé. On cherche des talents exceptionnels — passionnés de technologie, curieux par nature, exigeants par cnviction. Des gens pour qui explorer et innover est un réflexe, et qui veulent mettre leur énergie au service d'une mission qui va au-delà du développement du code et qui impacte des décisions, des processus, des humains. Directeur(trice) principal(e), R &D – Solutions cliniques Chez LGI Solutions Santé, nous ne faisons pas que développer des logiciels — nous permettons aux organisations de santé d’opérer avec confiance, précision et résilience. À titre de Directeur(trice) principal(e), R&D – Solutions cliniques, vous façonnerez la prochaine phase d’évolution de notre portefeuille clinique et aurez un impact mesurable sur le système de santé. À QUOI RESSEMBLERONT VOS JOURNÉES? Le rôle de Directeur(trice) principal(e), R&D – Solutions cliniques est responsable de l’exécution et de la performance opérationnelle du portefeuille clinique de LGI (15+ produits couvrant plusieurs piles technologiques), tout en contribuant aux décisions de portefeuille et d’architecture grâce à une collaboration étroite avec les équipes Produit, Architecture et le Chef de la direction R&D. Relevant du Chef de la direction R&D, vous dirigerez quatre gestionnaires R&D et superviserez plus de 60 employés (internes et consultants). Vous alignerez l’ingénierie sur les priorités corporatives, assurerez une exécution rigoureuse et améliorerez en continu la productivité, la qualité et la scalabilité. Vous êtes imputable d’une performance mesurable en production, garantissant que nos solutions cliniques demeurent fiables, sécuritaires et performantes au moment où cela compte le plus : dans des environnements de soins réels où la stabilité et la rapidité ont un impact direct sur la prestation des soins. COMMENT VOS CONTRIBUTIONS SERONT-ELLES MISES EN VALEUR? Leadership stratégique et vision * Définir et exécuter la stratégie R&D clinique alignée sur les priorités corporatives. * Collaborer avec les leaders en Architecture et en Produit pour orienter les choix technologiques; mettre en lumière les risques, les options et les propositions d’investissement liés à la dette technique, à la modernisation et à la pérennité. * Soutenir les décisions exécutives en structurant clairement les arbitrages (innovation, risque, coûts, délais et valeur à long terme). Excellence opérationnelle et impact * Assurer une livraison prévisible et de haute qualité à l’échelle du portefeuille. * Mettre en place une cadence de KPI couvrant la livraison, la productivité, les défauts et la performance en production. * Renforcer la surveillance, la discipline de mise en production et la gestion des incidents afin de réduire les défauts. * Déployer des outils, de l’automatisation et des pratiques augmentant l’efficacité de l’ingénierie. Organisation et talents * Concevoir et faire évoluer l’organisation pour maximiser l’impact et l’alignement. * Décliner les objectifs corporatifs en cibles d’équipe mesurables et gérer la performance avec rigueur. * Maintenir un haut niveau d’engagement tout en adressant la sous-performance avec fermeté. * Développer de manière proactive les capacités nécessaires à l’atteinte des objectifs du portefeuille par une planification stratégique de la main-d’œuvre, la gestion de la relève, des embauches ciblées et le développement continu des compétences. * Réduire les points uniques de défaillance par la documentation et la formation croisée. L’IA comme accélérateur stratégique * Promouvoir une adoption responsable et mesurable des outils d’IA pour accroître la productivité en ingénierie. * Identifier, piloter et déployer à grande échelle des cas d’usage IA à fort impact, avec des indicateurs de succès clairs et des mécanismes de contrôle des risques. ## Qualifications CE QUE VOUS APPORTEREZ À LGI SOLUTIONS SANTÉ POUR RÉUSSIR DANS CE RÔLE : • Plus de 15 ans d’expérience progressive en ingénierie logicielle, incluant la gestion de gestionnaires dans des environnements multi-produits. • Capacité démontrée à améliorer la performance de livraison, la stabilité en production et la productivité organisationnelle à grande échelle. • Une expérience en TI de la santé ou dans des environnements réglementés constitue un atout important. • Forte présence exécutive : à l’aise avec les parties prenantes de haut niveau; capable de simplifier des enjeux techniques complexes et d’influencer des décisions stratégiques. • Ce rôle exige une maîtrise complète du français et de l’anglais, puisque la personne sélectionnée travaillera avec de la documentation dans les deux langues et communiquera, à l’oral comme à l’écrit, avec des clients, partenaires, fournisseurs, collègues et parties prenantes internationales francophones et anglophones. LA RÉUSSITE DANS CE RÔLE SERA MESURÉE PAR UN IMPACT RÉEL ET VISIBLE : • Amélioration de la prévisibilité des livraisons et de la performance d’exécution. • Gains mesurables de productivité appuyés par des indicateurs clairs. • Réduction des incidents en production et des défauts en clientèle. • Fort engagement des équipes et résilience organisationnelle. ## Additional Information Pourquoi joindre LGI ? * Un environnement fondé sur la confiance, l'autonomie et la collaboration; * L’opportunité d’évoluer, de performer et de travailler avec des collègues curieux et talentueux; * Une culture d'apprentissage continu offrant du temps dédié à la formation, une plateforme reconnue de développement de vos compétences et l'accès à des outils de pointe; * Des projets stimulants qui contribuent à l'évolution des technologies de la santé et soutiennent le travail de plus de 320 000 professionnels, au bénéfice de plus de 6 millions de patients; * Un programme complet d'avantages sociaux incluant une assurance collective dès le premier jour, un REER collectif avec participation de l'employeur, la télémédecine 24/7, un programme d'aide aux employés et à leur famille, ainsi qu'un minimum de 3 semaines de vacances par année Chez LGI Solutions Santé, nous valorisons la diversité, l’équité et l’inclusion. Nous croyons que la diversité des expériences, des perspectives et des parcours contribue à notre succès. Nous nous engageons à favoriser un environnement de travail inclusif, équitable et respectueux, où chaque personne peut s’épanouir et réaliser son plein potentiel. Nous encourageons toutes les personnes qualifiées à soumettre leur candidature. Venez vous joindre à nous!", "summaryDescription" : "Directeur(trice) principal(e), R&D – Solutions cliniques at LGI Healthcare Solutions Santé Inc.. Skills: Clinical solutions, R&D leadership, AI strategy. Define clinical R&D strategy. Execute clinical R&D strategy", "postedDate" : "2026-06-15T15:54:36.000", "createdAt" : "2026-06-15T23:44:20.296", "lastUpdated" : "2026-06-16T08:43:32.814", "ingestTimestamp" : "2026-06-15T23:44:20.296", "mongoId" : "6a305d5df292fd229cf6631d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "KPI development", "Incident management", "Automation deployment", "Cross-functional alignment", "Performance management", "Risk control", "Leadership", "Vision", "Clinical solutions", "R&D leadership", "AI strategy", "Portfolio management", "Architecture decisions", "Technical debt", "Modernization", "Investment proposals", "Executive decision support", "Operational excellence", "Delivery execution", "Productivity improvement", "Quality improvement", "Scalability improvement", "Production performance", "Solution reliability", "Solution security", "Solution performance", "Solution stability", "Solution speed", "Organizational design", "Workforce planning", "Succession planning", "Skill development", "Cross-training", "Risk mitigation", "AI adoption", "AI deployment", "Roadmap development", "Portfolio decisions", "Healthcare solutions", "Clinical portfolio", "Health IT", "Regulated environments", "AI in healthcare" ], "skillCount" : 43, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Executive", "dataQualityScore" : 1.0, "_score" : 816.6167, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a305cb1f292fd229cf631f9", "title" : "Technicien d'Etudes cliniques H/F", "company" : "QIMA", "industry" : "Cosmetics", "salary" : { "min" : 38000.0, "max" : 52000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Research Technician in Nice, France, adjusted for the Biotech industry." }, "location" : "Nice, Provence-Alpes-Côte d'Azur, France", "locations" : [ "Nice", "Provence-Alpes-Côte d'Azur", "France" ], "timestamp" : "2026-06-16T08:00:39.216", "fingerprint" : "f86e799187fc8e6fb691feded41543949f7fe1c2951b1ff89479ec002f88b74a", "source" : "smartrecruiters", "language" : "fr", "applyUrl" : "https://jobs.smartrecruiters.com/QIMA/744000132226979-technicien-d-etudes-cliniques-h-f-", "externalId" : "744000132226979", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Nice", "state" : "Provence-Alpes-Côte d'Azur", "country" : "France", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "43.7009358,7.2683912" } ], "locationText" : "Nice, Provence-Alpes-Côte d'Azur, France", "employmentType" : "FULL_TIME", "minimumEducation" : "Associate's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Clinical data collection", "Patient recruitment", "Logistics management", "Clinical trial monitoring", "Data entry", "Laboratory sample management", "Procedure writing", "Technical sheet writing", "Instrument calibration", "Biomedical equipment maintenance", "Human biology analysis", "Medical supply management" ], "hardSkillsList" : [ "Clinical study follow-up", "Patient screening", "Consent collection", "Data management", "Investigator binder update", "Site initiation", "Mock report writing", "Subcontracting analysis" ], "softSkillsList" : [ "Relationship building", "Applied", "Curious", "Team spirit" ], "hardSkills" : [ { "name" : "Clinical study follow-up", "level" : "intermediate" }, { "name" : "Patient screening", "level" : "intermediate" }, { "name" : "Consent collection", "level" : "intermediate" }, { "name" : "Data management", "level" : "intermediate" }, { "name" : "Investigator binder update", "level" : "intermediate" }, { "name" : "Site initiation", "level" : "intermediate" }, { "name" : "Mock report writing", "level" : "intermediate" }, { "name" : "Subcontracting analysis", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Relationship building" }, { "name" : "Applied" }, { "name" : "Curious" }, { "name" : "Team spirit" } ], "majorSkills" : "Clinical study logistics, Data collection, Patient follow-up", "majorSkillsList" : [ "Clinical study logistics", "Data collection", "Patient follow-up" ], "coreResponsibilities" : "Assist investigator in patient follow-up, Participate in patient screening, Recruit patients, Apply products on skin, Take measurements, Prepare trial materials, Calibrate measurement instruments, Enter data into tools, Follow up with patients by phone, Manage patient logistics, Organize patient appointments, Manage treatment delivery, Manage patient visit flow, Manage lab sample collection, Prepare for ARC visits, Provide study documents, Manage corrections, Follow up on actions, Resolve clarification requests, Update investigator binder, Attend investigator meetings, Gather site initiation documents, Organize study setup visit, Write specific procedures, Write technical sheets, Participate in SMQ improvement, Participate in mock report writing, Manage instrument selection, Manage equipment qualification, Manage equipment use, Manage equipment maintenance, Manage biomedical equipment, Manage analysis subcontracting, Manage medical supplies, Manage research consumables", "teamCollaboration" : "ARC promoteur (moniteur); Data management; Investigator staff", "domainKnowledge" : "Clinical research; Pharmaceutical industry; Biotechnology; Cosmetics; Preclinical studies; Clinical studies; Drug development; Human biology analysis", "domainList" : [ "clinical-research", "pharmaceutical-industry", "biotechnology", "cosmetics", "preclinical-studies", "clinical-studies", "drug-development", "human-biology-analysis" ], "domainSpecificKnowledge" : [ "Clinical research", "Pharmaceutical industry", "Biotechnology", "Cosmetics", "Preclinical studies", "Clinical studies", "Drug development", "Human biology analysis" ], "toolProficiency" : [ "Office tools" ], "communicationSkills" : "Written French; Oral French; Written English", "documentationSkills" : "Investigator binder; Procedures; Technical sheets; Mock reports", "problemSolvingSkills" : "Resolve clarification requests", "specialRequirements" : "Hospital environment", "qualificationsBasic" : "Bac+3/5 scientific or medical, Bac+2 with 3 years clinical research, Maitrise French written and oral (B2), Good knowledge office tools, Good understanding written English (B2)", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Chez QIMA, notre mission quotidienne est d'offrir des services qui permettent à nos clients de prouver la conformité et l’efficacité de leurs produits. Présents dans plus de 100 pays, nous servons les industries de produits de consommation, de l'alimentation et des sciences de la vie et aidons plus de 30 000 marques, détaillants, fabricants et producteurs à atteindre l'excellence en matière de qualité. Nous combinons expertise sur le terrain, solutions numériques et recherche scientifique afin de garantir des données conformes et fiables à nos clients. Nos 5 000 collaborateurs travaillent chaque jour selon nos valeurs. Avec la passion du client, l'intégrité et un engagement à simplifier les process, nous avons transformé l'industrie des Tests, Inspections et Certifications. QIMA Life Sciences accompagne les leaders mondiaux des industries pharmaceutiques, biotechnologiques et cosmétiques grâce à une offre de tests et de modèles précliniques et cliniques scientifiquement validés. Nos solutions permettent, dès les premières étapes, d’identifier les candidats médicaments, formules ou ingrédients actifs les plus prometteurs. Elles contribuent ainsi à optimiser les ressources, accélérer le développement et améliorer les taux de succès. Partenaire de confiance, notre expertise scientifique nous permet de fournir à nos clients des données robustes, indispensables à des prises de décision éclairées et au développement de l’innovation. Votre rôle En tant que Technicien d’Etudes cliniques, vous gérez la logistique et le recueil des données des études cliniques dans le respect de la réglementation et des délais au niveau du site investigateur. Missions principales Suivi des études cliniques * Assister l’investigateur dans le suivi clinique des patients. * Participer au screening et au recrutement des patients, pouvant inclure une présentation brève de l’étude préliminaire aux explications et au recueil du consentement par l’investigateur * Appliquer des produits sur la peau des volontaires et prendre des mesures * Préparer et utiliser le matériel nécessaire aux essais et instruments de mesures (réglage, calibration…) * Saisir des données dans les différents outils mis en place avec le promoteur * Assurer le suivi téléphonique des patients et des relances pour le suivi des visites * Gérer la logistique des patients inclus dans l’étude : organisation des rendez-vous avec les différents services, gestion du circuit de la délivrance des traitements, organisation du déroulé de chaque visite patient, gestion des prélèvements de laboratoire (préparation, stockage et acheminement) * Participer aux visites de monitoring de l’ARC promoteur (moniteur) * Préparer la visite et la mise à disposition des documents relatifs à l’étude * Gérer les corrections et le suivi des actions en présence de l’ARC promoteur (moniteur) * Résoudre les différentes demandes de clarification provenant du Data management ou de l’ARC promoteur (moniteur) en cours d’étude Gestion administrative de l’étude au niveau du centre investigateur * Mettre à jour le classeur investigateur * Participer si besoin aux réunions investigateurs et/ou de staff * Recueillir les documents nécessaires à l’initiation du site en coordination avec l’ARC promoteur (moniteur) * Organiser et participer à la visite de mise en place de l’étude * Rédiger des procédures et des fiches techniques spécifiques au protocole à destination de l’équipe sur le centre * Participer à l’amélioration du SMQ Missions Complémentaires * Participer à la rédaction des « mock reports » * Gérer la sélection, qualification, suivi, utilisation, maintenance des instruments de mesures et équipement biomédical * Gérer la sous-traitance des analyses de biologie humaine * Gérer les fournitures médicales et consommables de recherche * Participer à la relecture des rapports finaux ## Qualifications Savoir-faire * Bac+3/5 dans le domaine scientifique ou médical ou Bac+2 avec 3 ans expérience en recherche clinique ; * Maitrise du français écrit et oral (niveau B2) ; * Bonnes connaissances des outils bureautiques pour la saisie de données ; * Bonne compréhension de l’anglais écrit (niveau B2). Savoir-être * Très bon sens du relationnel afin d’accueillir et accompagner les participants ; * Profil appliqué et curieux, bon esprit d’équipe. ## Additional Information Contrat * Offre : CDI, à temps plein * Statut : Technicien * Lieu du poste : Nice, en milieu hospitalier * Disponibilité : dès que possible Rémunération : * Rémunération selon la grille conventionnelle de la Convention collective nationale des Industries Pharmaceutiques - IDCC 176.", "summaryDescription" : "Technicien d'Etudes cliniques H/F at QIMA. Skills: Clinical study logistics, Data collection, Patient follow-up. Assist investigator in patient follow-up. Participate in patient screening", "postedDate" : "2026-06-15T14:58:48.000", "createdAt" : "2026-06-16T00:02:21.894", "lastUpdated" : "2026-06-16T08:00:39.216", "ingestTimestamp" : "2026-06-16T00:02:21.894", "mongoId" : "6a305cb1f292fd229cf631f9", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Clinical study follow-up", "Patient screening", "Consent collection", "Data management", "Investigator binder update", "Site initiation", "Mock report writing", "Subcontracting analysis", "Relationship building", "Applied", "Curious", "Team spirit", "Clinical study logistics", "Data collection", "Patient follow-up", "Clinical data collection", "Patient recruitment", "Logistics management", "Clinical trial monitoring", "Data entry", "Laboratory sample management", "Procedure writing", "Technical sheet writing", "Instrument calibration", "Biomedical equipment maintenance", "Human biology analysis", "Medical supply 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"fingerprint" : "ee2616b6e6b17c65bf330112cde7fbf35a5f8c252b060b0da9b9fd4ec9887500", "source" : "smartrecruiters", "language" : "fr", "applyUrl" : "https://jobs.smartrecruiters.com/QIMA/744000132226979-technicien-d-etudes-cliniques-h-f-", "externalId" : "744000132226979", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Nice", "state" : "Provence-Alpes-Côte d'Azur", "country" : "France", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "43.7009358,7.2683912" } ], "locationText" : "Nice, Provence-Alpes-Côte d'Azur, France", "employmentType" : "FULL_TIME", "minimumEducation" : "Associate's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Clinical data collection", "Patient recruitment", "Logistics management", "Clinical trial monitoring", "Data entry", "Laboratory sample management", "Procedure writing", "Technical sheet writing", "Instrument calibration", "Biomedical equipment management", "Human biology analysis", "Medical supply management" ], "hardSkillsList" : [ "Clinical study follow-up", "Patient screening", "Consent collection", "Data management", "Investigator binder update", "Site initiation", "Mock report writing", "Subcontracting analysis" ], "softSkillsList" : [ "Relationship building", "Applied", "Curious", "Team spirit" ], "hardSkills" : [ { "name" : "Clinical study follow-up", "level" : "intermediate" }, { "name" : "Patient screening", "level" : "intermediate" }, { "name" : "Consent collection", "level" : "intermediate" }, { "name" : "Data management", "level" : "intermediate" }, { "name" : "Investigator binder update", "level" : "intermediate" }, { "name" : "Site initiation", "level" : "intermediate" }, { "name" : "Mock report writing", "level" : "intermediate" }, { "name" : "Subcontracting analysis", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Relationship building" }, { "name" : "Applied" }, { "name" : "Curious" }, { "name" : "Team spirit" } ], "majorSkills" : "Clinical study logistics, Data collection, Patient follow-up", "majorSkillsList" : [ "Clinical study logistics", "Data collection", "Patient follow-up" ], "coreResponsibilities" : "Assist investigator in patient follow-up, Participate in patient screening, Recruit patients, Apply products on skin, Take measurements, Prepare trial materials, Use measurement instruments, Calibrate instruments, Enter data in tools, Follow up patients by phone, Manage patient logistics, Organize patient appointments, Manage treatment delivery, Organize patient visit flow, Manage lab sample collection, Prepare lab samples, Store lab samples, Ship lab samples, Participate in ARC monitoring visits, Prepare study documents, Manage corrections, Follow up actions, Resolve clarification requests, Update investigator binder, Participate in investigator meetings, Gather site initiation documents, Organize study setup visit, Participate in setup visit, Write specific procedures, Write specific technical sheets, Participate in SMQ improvement, Participate in mock report writing, Manage instrument selection, Manage equipment qualification, Manage equipment follow-up, Manage equipment use, Manage equipment maintenance, Manage biomedical equipment, Manage subcontracting, Manage human biology analysis, Manage medical supplies, Manage research consumables", "teamCollaboration" : "ARC promoteur (moniteur); Data management; Investigator staff", "domainKnowledge" : "Clinical research; Pharmaceutical industry; Biotechnology; Cosmetics; Preclinical testing; Clinical testing; Drug candidates; Active ingredients; Human biology analysis", "domainList" : [ "clinical-research", "pharmaceutical-industry", "biotechnology", "cosmetics", "preclinical-testing", "clinical-testing", "drug-candidates", "active-ingredients", "human-biology-analysis" ], "domainSpecificKnowledge" : [ "Clinical research", "Pharmaceutical industry", "Biotechnology", "Cosmetics", "Preclinical testing", "Clinical 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Présents dans plus de 100 pays, nous servons les industries de produits de consommation, de l'alimentation et des sciences de la vie et aidons plus de 30 000 marques, détaillants, fabricants et producteurs à atteindre l'excellence en matière de qualité. Nous combinons expertise sur le terrain, solutions numériques et recherche scientifique afin de garantir des données conformes et fiables à nos clients. Nos 5 000 collaborateurs travaillent chaque jour selon nos valeurs. Avec la passion du client, l'intégrité et un engagement à simplifier les process, nous avons transformé l'industrie des Tests, Inspections et Certifications. QIMA Life Sciences accompagne les leaders mondiaux des industries pharmaceutiques, biotechnologiques et cosmétiques grâce à une offre de tests et de modèles précliniques et cliniques scientifiquement validés. Nos solutions permettent, dès les premières étapes, d’identifier les candidats médicaments, formules ou ingrédients actifs les plus prometteurs. Elles contribuent ainsi à optimiser les ressources, accélérer le développement et améliorer les taux de succès. Partenaire de confiance, notre expertise scientifique nous permet de fournir à nos clients des données robustes, indispensables à des prises de décision éclairées et au développement de l’innovation. Votre rôle En tant que Technicien d’Etudes cliniques, vous gérez la logistique et le recueil des données des études cliniques dans le respect de la réglementation et des délais au niveau du site investigateur. Missions principales Suivi des études cliniques * Assister l’investigateur dans le suivi clinique des patients. * Participer au screening et au recrutement des patients, pouvant inclure une présentation brève de l’étude préliminaire aux explications et au recueil du consentement par l’investigateur * Appliquer des produits sur la peau des volontaires et prendre des mesures * Préparer et utiliser le matériel nécessaire aux essais et instruments de mesures (réglage, calibration…) * Saisir des données dans les différents outils mis en place avec le promoteur * Assurer le suivi téléphonique des patients et des relances pour le suivi des visites * Gérer la logistique des patients inclus dans l’étude : organisation des rendez-vous avec les différents services, gestion du circuit de la délivrance des traitements, organisation du déroulé de chaque visite patient, gestion des prélèvements de laboratoire (préparation, stockage et acheminement) * Participer aux visites de monitoring de l’ARC promoteur (moniteur) * Préparer la visite et la mise à disposition des documents relatifs à l’étude * Gérer les corrections et le suivi des actions en présence de l’ARC promoteur (moniteur) * Résoudre les différentes demandes de clarification provenant du Data management ou de l’ARC promoteur (moniteur) en cours d’étude Gestion administrative de l’étude au niveau du centre investigateur * Mettre à jour le classeur investigateur * Participer si besoin aux réunions investigateurs et/ou de staff * Recueillir les documents nécessaires à l’initiation du site en coordination avec l’ARC promoteur (moniteur) * Organiser et participer à la visite de mise en place de l’étude * Rédiger des procédures et des fiches techniques spécifiques au protocole à destination de l’équipe sur le centre * Participer à l’amélioration du SMQ Missions Complémentaires * Participer à la rédaction des « mock reports » * Gérer la sélection, qualification, suivi, utilisation, maintenance des instruments de mesures et équipement biomédical * Gérer la sous-traitance des analyses de biologie humaine * Gérer les fournitures médicales et consommables de recherche * Participer à la relecture des rapports finaux ## Qualifications Savoir-faire * Bac+3/5 dans le domaine scientifique ou médical ou Bac+2 avec 3 ans expérience en recherche clinique ; * Maitrise du français écrit et oral (niveau B2) ; * Bonnes connaissances des outils bureautiques pour la saisie de données ; * Bonne compréhension de l’anglais écrit (niveau B2). Savoir-être * Très bon sens du relationnel afin d’accueillir et accompagner les participants ; * Profil appliqué et curieux, bon esprit d’équipe. ## Additional Information Contrat * Offre : CDI, à temps plein * Statut : Technicien * Lieu du poste : Nice, en milieu hospitalier * Disponibilité : dès que possible Rémunération : * Rémunération selon la grille conventionnelle de la Convention collective nationale des Industries Pharmaceutiques - IDCC 176.", "summaryDescription" : "Technicien d'Etudes cliniques H/F at QIMA. Skills: Clinical study logistics, Data collection, Patient follow-up. Assist investigator in patient follow-up. 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management", "Clinical research", "Pharmaceutical industry", "Biotechnology", "Cosmetics", "Preclinical testing", "Clinical testing", "Drug candidates", "Active ingredients", "Office tools" ], "skillCount" : 36, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "_score" : 733.6927, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c958974d8ee00a098d54e", "title" : "Clinical Trial Manager/Sr Clinical Trial Manager", "company" : "Erasca", "industry" : "Biotech", "salary" : { "min" : 7500000.0, "max" : 1.2E7, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimation is based on the US market baseline for a Senior Clinical Trial Manager in the Biotech industry, adjusted for seniority and remote work." }, "location" : "Remote", "locations" : [ "Remote", "San Diego", "California", "United States" ], "timestamp" : "2026-06-15T10:14:23.389", "fingerprint" : "c975d251af2caa4429c4423c0496abc8f5007b5b44d7edf8823037316a85b7eb", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/erasca/jobs/7767584003", "externalId" : "7767584003", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "experienceLevel" : "Manager", "technicalSkills" : "Electronic data capture, Data management software", "professionalSkills" : [ "Trial management", "Resource planning", "Budget management", "Contract negotiation", "Vendor management", "Cross-functional coordination", "Process management", "Continuous improvement", "Stakeholder management" ], "hardSkillsList" : [ "Clinical trial execution", "Clinical trial management", "Clinical operations" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Clinical trial execution", "level" : "intermediate" }, { "name" : "Clinical trial management", "level" : "intermediate" }, { "name" : "Clinical operations", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Clinical trial management, Oncology indications, Vendor management", "majorSkillsList" : [ "Clinical trial management", "Oncology indications", "Vendor management" ], "coreResponsibilities" : "Manage global clinical trials, Recruit global study sites, Foster relationships with study investigators, Participate in site selection, Participate in vendor selection, Participate in site qualification, Participate in vendor qualification, Participate in site activation, Develop Requests-for-Proposals, Assist in vendor selection efforts, Assist in review vendor contracts, Assist in negotiation vendor contracts, Assist in review study site agreements, Assist in negotiation study site agreements, Manage study vendors, Monitor trial progress, Track trial enrollment, Track clinical trial material inventory, Review monitoring visit reports, Assist in packaging clinical trial material, Assist in labeling clinical trial material, Assist in distribution clinical trial material, Monitor biological samples, Track biological samples, Provide progress updates to management, Provide progress updates during meetings, Assist in departmental budgeting, Assist in accruals, Assist in projections, Assist in development protocols, Assist in development consent forms, Assist in development IRB/EC materials, Assist in development trial documents, Assist in development Clinical SOPs, Prepare study materials, Review study materials, Approve study materials, Assist in electronic case report form design, Assist in electronic case report form development, Assist in IRT design, Assist in IRT development, Participate in data cleaning, Develop appropriate data outputs, Fulfill needs of other Erasca departments, Provide leadership to team members, Perform duties in keeping with core values, Perform duties in keeping with policies, Perform duties in keeping with regulations", "teamCollaboration" : "Global multi-disciplinary teams; Program team meetings; Other Erasca departments", "projectManagementSkills" : [ "Clinical trial management", "Project management", "Priority management" ], "domainKnowledge" : "Oncology indications; RAS/MAPK pathway; ICH-GCP; FDA regulations; Regulatory agency requirements", "domainList" : [ "oncology-indications", "ras-mapk-pathway", "ich-gcp", "fda-regulations", "regulatory-agency-requirements" ], "domainSpecificKnowledge" : [ "Oncology indications", "RAS/MAPK pathway", "ICH-GCP", "FDA regulations", "Regulatory agency requirements" ], "toolProficiency" : [ "IRT", "ECG", "Electronic data capture" ], "communicationSkills" : "Oral communication; Written communication", "documentationSkills" : "Clinical documentation; Protocols; Consent forms; IRB/EC materials; CRFs; Patient diaries; Drug accountability forms; Study manuals; Investigator manuals; Project plans; Monitoring reports; SOPs", "continuousLearning" : "Learning orientation", "qualificationsBasic" : "5 years of relevant experience, 7 years of relevant experience, ICH-GCP guidelines experience, US and ex-US regulations experience, Electronic data capture experience, Data management software experience, Clinical Research Associates management experience, Reviewing monitoring trip reports experience", "qualificationsPreferred" : "Undergraduate degree in life sciences", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer. The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation, and management of clinical studies from concept to completion. The position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out, including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources, budgets, contracts, and timelines. Essential Duties and Responsibilities: Manage global clinical trials (Phase 1-3) in oncology indications, ensuring that studies are carried out in accordance with the clinical development plan, ICH-GCP, and FDA/other regulatory agency requirements. Recruit global study sites and foster relationships with study investigators. Participate in the process of site and vendor selection, qualification, and activation. Develop Requests-for-Proposals and assist in vendor selection efforts. Assist in review and negotiation of vendor contracts and study site clinical trial agreements. Manage study vendors (e.g., CRO, IRT, laboratories, core ECG/imaging). Monitor the progress of trials, including enrollment and clinical trial material inventory. Review monitoring visit reports for completeness and adherence to the annotations. Assist in packaging/labeling/distribution of clinical trial material. Monitor and track biological samples for applicable analyses. Provide progress updates to management and during program team meetings. Assist in departmental budgeting, including accruals and projections. Assist in development of protocols, consent forms, IRB/EC materials, and other trial documents. Assist in development of Clinical SOPs. Prepare/review/approve study materials such as CRFs, patient diaries, drug accountability forms, study and investigator manuals, project plans, and monitoring reports. Assist in electronic case report form design and development.  Assist in IRT design and development. Participate in data cleaning activities and developing appropriate data outputs. Understand and help fulfill the needs of other Erasca departments (e.g., Finance, Research). Provide leadership and mentoring of other Clinical team members. Perform all duties in keeping with the Company’s core values, policies and all applicable regulations. Required Education, Experience and Attributes: Preferred undergraduate degree in life sciences or professions (pharmacy, medicine, nursing, or other allied health sciences). For Clinical Trial Manager, at least 5 years of relevant experience in oncology clinical operations in pharmaceutical company or CRO including trial set-up, monitoring, and close-out of US and non-US trials at all phases of pre-NDA clinical research (Phases 1-3). For Senior Clinical Trial Manager, at least 7 years of relevant experience required. Demonstrated excellence in trial management skills, with track record of successfully managing multiple projects, trials, and priorities. Experience with managing study vendors (e.g., CRO, IRT, laboratories, core ECG/imaging). Ability to work well with global, multi-disciplinary teams. Experience in practical knowledge and implementation of ICH-GCP guidelines and US and ex-US regulations. Experience with electronic data capture and data management software. Experience in the management of Clinical Research Associates. Excellent oral and written communication skills. Experience with reviewing monitoring trip reports Must be able to thrive in an entrepreneurial, fast-paced, and dynamic work environment. Must be organized and be able to communicate effectively. Must be a self-starter. Strong learning orientation, curiosity, and commitment to science and patients. The anticipated salary range for this position is $145,000 to $190,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etcetera. In addition to base salary, the hired applicant will be eligible to receive an annual bonus and an equity grant at hire and annually in the form of the option to purchase stock in the future for a specified price. Along with our casual, collaborative, and fun work and the chance to make your mark in our mission to erase cancer, Erasca offers a comprehensive and competitive benefits package that includes: Paid Time Off, Holiday, and Sick Leave, Medical, Dental and Vision Plans, Short- and Long-Term Disability, Basic and Voluntary Life/AD&D Coverage, Flexible Spending Accounts (FSA, HSA, and Commute), Critical Illness and Accident Coverage, Pet Insurance, Employee Assistance Program, 401(k) Plan with Erasca contribution, and the opportunity to participate in an Employee Stock Purchase Program. Erasca, Inc., is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of sex , race, religion, national origin, ancestry, physical or mental disability, protected medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law or ordinance or regulation.", "summaryDescription" : "Clinical Trial Manager/Sr Clinical Trial Manager at Erasca. Skills: Clinical trial management, Oncology indications, Vendor management. Manage global clinical trials. Recruit global study sites", "postedDate" : "2026-06-13T20:50:54.917", "createdAt" : "2026-06-13T20:50:54.917", "lastUpdated" : "2026-06-15T10:14:23.389", "ingestTimestamp" : "2026-06-13T20:50:54.917", "mongoId" : "6a2c958974d8ee00a098d54e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 7500000, "salaryAnnualMax" : 12000000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Clinical trial execution", "Clinical trial management", "Clinical operations", "Leadership", "Mentoring", "Oncology indications", "Vendor management", "Trial management", "Resource planning", "Budget management", "Contract negotiation", "Cross-functional coordination", "Process management", "Continuous improvement", "Stakeholder management", "Project management", "Priority management", "RAS/MAPK pathway", "ICH-GCP", "FDA regulations", "Regulatory agency requirements", "IRT", "ECG", "Electronic data capture" ], "skillCount" : 24, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "_score" : 733.6392, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a307ba9f292fd229c047452", "title" : "Assistant/Assistante marketing et communication - Pôle Visiteurs - Alternance", "company" : "RX France", "salary" : { "min" : 20000.0, "max" : 24000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimation is based on the market baseline for an entry-level marketing and communication internship in France, with adjustments for the media industry and the specific company." }, "location" : "France", "locations" : [ "France" ], "timestamp" : "2026-06-16T13:14:32.686", "fingerprint" : "a888b2323e039ad9d3a806aaad62d034fd1b059100a020633348096283e060e0", "source" : "workday", "language" : "fr", "applyUrl" : "https://relx.wd3.myworkdayjobs.com/ReedExhibitions/job/FRANCE---Tour-Vista/Assistant-Assistante-marketing-et-communication---Ple-Visiteurs_R114519", "externalId" : "R114519", "industryFunction" : { }, "locationPoint" : "46.2276,2.2137", "structuredLocations" : [ { "country" : "France", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "France", "employmentType" : "FULL_TIME", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "[_RX France_](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Frxglobal.com%2Frx-france&data=05%7C02%7CFrederique.LEBRIS%40rxglobal.com%7C62820a5b8ff342ef640d08debcabe938%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C639155643782295059%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=Xthpku77iytgJ85OZCjA7nqAqzifJ1OVgOg6zZ5aOIk%3D&reserved=0) est créateur de places de rencontres à forte valeur ajoutée, leader sur une quinzaine de marchés différents. Parmi les salons emblématiques de RX France et incontournables sur le plan national et international, figurent MIPIM, MAPIC, Batimat, Pollutec, EquipHotel, SITL, IFTM, Big Data & AI Paris, MIPCOM, Paris Photo et bien d’autres… Nos événements se déroulent en France, à Hong Kong, en Italie et au Mexique. Pour plus d'informations sur [_www.rxglobal.fr_](https://nam11.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.rxglobal.fr%2F&data=05%7C02%7CFrederique.LEBRIS%40rxglobal.com%7C62820a5b8ff342ef640d08debcabe938%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C639155643782317930%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=OREbh%2BpbrN5WZ47UXvhq4qFcVr0Z%2FeU%2Fh2qhXQzRgSc%3D&reserved=0) RX France recherche activement un(e) **Assistant/Assistante marketing et communication en Alternance** pour rejoindre les équipes marketing du pôle visiteurs. ** _Description du poste_** Au sein des équipes marketing, vous participerez au suivi du plan marketing de chaque salon sur les thématiques suivantes : **Marketing :** Réflexion et création contenu newsletters partenaires Mise à jour et création de documents Veille marché Sur site, accueil des partenaires, gestion de visites guidées, création des badges, service client onsite exposants et visiteurs etc. **Communication :** Site internet : mise à jour et optimisation des contenus du site internet Plan marketing relationnel : création des emails suivant la charte établie et les contenus donnés Réseaux Sociaux : accompagnement pour la récupération des contenus auprès des équipes en interne et des partenaires Outils de communication : être le garant de la bonne mise en œuvre des différents outils de com vendus et deals de partenariats Accompagnement sur site pour la gestion des prestataires (photos, vidéos, RS, agence de presse, hôtesses) ** _Profil_** Vous êtes organisé, rigoureux et autonome. Vous avez une appétence pour le digital. Vous êtes polyvalent, avez le sens du service et du client ainsi que le goût pour le travail en équipe. Votre anglais est courant. **_Qui sommes-nous_** __ : Chez RX France, nous sommes passionnés par l'idée d'avoir un impact positif sur la société et nos clients grâce à la puissance de la rencontre. Nous créons des places de rencontres à très haute valeur ajoutée pour 15 secteurs d’activité, à travers des salons emblématiques tels que MIPIM, Mondial du Bâtiment, Pollutec, MIPCOM, Paris Photo, et bien d'autres. En rejoignant RX France, vous ferez partie d'une entreprise qui valorise la diversité et l'inclusion. Nous nous engageons à créer un environnement de travail juste et équitable pour nos collaborateurs, indépendamment de leur sexe, de leur identité sexuelle, de leur origine, de leur religion, de leur orientation sexuelle, de leur âge ou de leur handicap. Tous nos postes sont ouverts aux personnes en situation de handicap et nous sommes prêts à mettre en place des aménagements pour faciliter le processus de recrutement. De plus, toutes les personnes, indépendamment de leur genre, recevront un traitement équitable en matière de rémunération. Rejoignez-nous chez RX France et contribuez à notre mission d'offrir une expérience magique et impactante à nos clients, en multipliant leurs opportunités de business. Primary Location Base Pay Range: FRANCE - Tour Vista €13 900 - €23 400. **We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. Click**[** _here_**](https://www.relx.com/careers/join-us/benefits)**to access benefits specific to your location.** We are committed to providing a fair and accessible hiring process. 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Learn more about spotting and avoiding scams**[**here**](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fstories.relx.com%2Fhow-to-avoid-job-scams%2Findex.html&data=05%7C02%7CSharon.Martin%40lexisnexis.com%7C2104edc7df90474aaf1108dd8cccf948%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C638821534169036749%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=bMcV1zP1yRXUuNWYwyGuPPb7lCyTuoA%2BGPT0d5MfO8I%3D&reserved=0)**.** Please read our [Candidate Privacy Policy](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.relx.com%2Fcareers%2Fjoin-us%2Fprivacy&data=05%7C02%7CSharon.Martin%40lexisnexis.com%7C2104edc7df90474aaf1108dd8cccf948%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C638821534169045885%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=X%2BrqkisseFh6q%2BEqRLuRvCa2dfT9Q2QeATdfGRVQxnI%3D&reserved=0). We are an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law. _**USA Job Seekers:**_ [EEO Know Your Rights](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.eeoc.gov%2Fsites%2Fdefault%2Ffiles%2F2023-06%2F22-088_EEOC_KnowYourRights6.12.pdf&data=05%7C02%7CSharon.Martin%40lexisnexis.com%7C2104edc7df90474aaf1108dd8cccf948%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C638821534169055021%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=mEoTzyFpKtgiRgZnquZyELr%2FkuMrW4%2F9zYB4HMS4hdI%3D&reserved=0).", "summaryDescription" : "Assistant/Assistante marketing et communication - Pôle Visiteurs - Alternance at RX France", "postedDate" : "2026-06-16T03:58:50.947", "createdAt" : "2026-06-16T03:58:50.942", "lastUpdated" : "2026-06-16T13:14:32.686", "ingestTimestamp" : "2026-06-16T03:58:50.942", "mongoId" : "6a307ba9f292fd229c047452", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://relx.wd3.myworkdayjobs.com/ReedExhibitions/job/FRANCE---Tour-Vista/Assistant-Assistante-marketing-et-communication---Ple-Visiteurs_R114519", "salaryBand" : "<30k", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "marketing", "jobSubcategory" : "growth", "seniorityLevel" : "mid", "dataQualityScore" : 0.7777778, "_score" : 693.4184, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Media", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c972974d8ee00a0991a6c", "title" : "Clinical Trial Manager", "industry" : "Healthcare", "salary" : { "min" : 115000.0, "max" : 175000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Clinical Trial Manager in the United States, adjusted for manager seniority and the biotech industry." }, "location" : "(Multiple States)", "locations" : [ "(Multiple States)" ], "timestamp" : "2026-06-15T06:53:27.929", "fingerprint" : "146c58794f3f4adcc09cf0d8eee62c8cdb827db4937f81c01797aaee4a21bb10", "source" : "jazzhr", "language" : "en", "externalId" : "FvtRpZSiZS", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "United States", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Operational metrics" ], "hardSkills" : [ { "name" : "Operational metrics", "level" : "intermediate" } ], "majorSkills" : "Process management, Cross-functional coordination, Vendor management, Stakeholder management", "majorSkillsList" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management" ], "coreResponsibilities" : "Manage processes, Coordinate cross-functionally, Manage vendors, Manage stakeholders, Plan resources, Improve continuously", "teamCollaboration" : "Cross-functional teams; Stakeholder engagement", "domainKnowledge" : "Clinical trials", "domainList" : [ "clinical-trials" ], "domainSpecificKnowledge" : [ "Clinical trials" ], "summaryDescription" : "Clinical Trial Manager. Skills: Process management, Cross-functional coordination, Vendor management, Stakeholder management. Manage processes. 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Positioned between the Clinical Trial Associate (CTA) a", "summaryDescription" : "Clinical Trial Management Associate (CTMA), Oncology (EMEA/LATAM) at Maleda Tech. Skills: Clinical trial management. Oversee oncology clinical trials. Execute oncology clinical trials", "createdAt" : "2026-06-14T21:48:06.104", "lastUpdated" : "2026-06-16T03:38:06.688", "ingestTimestamp" : "2026-06-14T21:48:06.104", "mongoId" : "6a2c9f2374d8ee00a099f5d4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 110000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Clinical trial management", "Clinical operations", "Oncology clinical trials", "EMEA", "LATAM" ], "skillCount" : 5, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 665.1103, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c8cf574d8ee00a0977c58", "title" : "Program Manager, Clinical Trial Operations", "company" : "myTomorrows", "industry" : "Operations", "salary" : { "min" : 125000.0, "max" : 175000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Mid-level Program Manager, Clinical Trial Operations in the US Healthcare industry, adjusted for remote work and manager experience." }, "location" : "US, Remote ", "locations" : [ "US, Remote ", "Canada " ], "timestamp" : "2026-06-16T04:24:55.804", "fingerprint" : "e4edd365e40121af68220ecc7b360b02d435e8159745e2be0b87ea34a2ffa246", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/mytomorrows/c6be63e2-4f96-4299-a20b-3ac72d0b4f5a/application", "externalId" : "c6be63e2-4f96-4299-a20b-3ac72d0b4f5a", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options. We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem. We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection. With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business. Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. The opportunity: Program Manager - Clinical Trial Operations As a Program Manager, your main responsibility is to ensure (global) access to clinical trials via smooth running digital patient recruitment and pre-screening programs. The aim of our patient recruitment programs is to (1) increase patients’ and physicians’ clinical trial awareness and understanding, (2) pre-screen patients to assess their potential clinical trial eligibility, (3) provide high-quality patient referrals to clinical trial sites and 4) ultimately boost patient enrollment rates. You will serve as the first point of contact for pharmaceutical and biotech partners, providing end‑to‑end oversight of all patient recruitment program activities. You will ensure timely and high‑quality delivery of patient recruitment programs by coordinating stakeholders and driving effective, compliant patient engagement from first contact to site referral and enrollment. You will be supported by cross-functional experts across Patient Navigation, Medical Community, Marketing, Product and Engineering. Geographic Requirement: To ensure seamless collaboration with our teams, applicants must reside within the EST or CST time zones. WHAT YOU'LL DO IN THIS ROLE: - Be the primary contact person for our BioPharma clients and internal stakeholders for the patient recruitment programs under your responsibility - Be responsible for the onboarding and launch of new programs, including overseeing the development of patient recruitment materials (e.g., clinical trial landing pages with pre-screening questionnaires) - Ensure a smooth-running program and insight-driven reporting - Keep (financial) oversight of the program and manage all the ongoing activities and communication - Create detailed timelines including deliverables, milestones and objectives and ensure that deadlines are being met - Develop strong relations and trust with all stakeholders and keep them up to date on the progress of your programs - Achieve and maintain high customer satisfaction - Develop and advise on solutions to tackle operational issues along with relevant subject matter experts - Contribute to improving our patient recruitment and pre-screening processes and strategies - Support overall myTomorrows program performance and operations, as needed. WHAT YOU BRING TO THE TABLE: - University degree in Life Sciences/Healthcare (preferred) - 2+ years of trial / project management experience within the pharmaceutical industry / CROs - Thorough understanding of clinical research and clinical trial patient recruitment - Proven ability to manage complex, cross-functional programs with multiple internal and external stakeholders, ensuring timely delivery and budget oversight - Experience leading client-facing programs, including managing expectations, communicating progress, and serving as a trusted partner to Sponsors and sites - Strong communication and diplomatic skills, with the ability to navigate sensitive situations, balance stakeholder interests, and maintain productive long‑term relationships - A commercial mindset, with the ability to understand commercial drivers, track program financials, and contribute to strategic decision‑making - Basic understanding of how web pages and search engine ads function, to ensure a smooth collaboration with the Marketing and Product & Engineering teams - A good eye for detail; thinking in processes/operations comes natural to you - Able to prioritize, analyze issues, optimize processes and find / recommend alternative solutions - Excellent verbal and written communication skills in English WHAT SUCCESS IN THE FIRST 6 MONTHS LOOKS LIKE: - At least one-two patient recruitment program launched on time, operating smoothly. - A sustained flow of high-quality, pre‑screened referrals meeting protocol-specific criteria, with clear conversion from inquiry to enrollment. - Strong client relationships, evidenced by NPS > 50 and no escalations. - Seamless collaboration with other teams incl. Patient Navigation, Medical Community, Marketing, Product & Engineering. WHAT WE OFFER: - Impactful work that helps patients gain access to potentially lifesaving treatments. - International work environment, scale-up energy and a flat organizational structure that encourages creativity and accountability. - Competitive salary, annual performance bonus and an Employee Stock Option Plan. - Great career development opportunities in a fast-growing company. - Learning and development budget alongside internal knowledge sharing sessions. - Attractive pension plan, full premium covered by myTomorrows. - Hybrid working model. - Policies to support working parents. - Healthy lunch at the thriving Amsterdam office. - Unlimited access to professional guidance by certified psychologists via OpenUp - Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration! Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that. ", "summaryDescription" : "Program Manager, Clinical Trial Operations at myTomorrows", "createdAt" : "2026-06-14T19:28:16.237", "lastUpdated" : "2026-06-16T04:24:55.804", "ingestTimestamp" : "2026-06-14T19:28:16.237", "mongoId" : "6a2c8cf574d8ee00a0977c58", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 125000, "salaryAnnualMax" : 175000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 662.0176, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a307ba9f292fd229c04744e", "title" : "Assistant/Assistante marketing et communication - Pôle Audiences Stratégiques - Alternance", "company" : "RX France", "salary" : { "min" : 12000.0, "max" : 18000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an entry-level Marketing and Communication Assistant internship in France, adjusted for the media industry." }, "location" : "France", "locations" : [ "France" ], "timestamp" : "2026-06-16T11:50:41.633", "fingerprint" : "e026d676457401ac4d4fd545d97c3f3017f4683526f662231e04bea9e24971a1", "source" : "workday", "language" : "fr", "applyUrl" : "https://relx.wd3.myworkdayjobs.com/ReedExhibitions/job/FRANCE---Tour-Vista/Assistant-Assistante-marketing-et-communication---Ple-Audiences-Stratgiques---Alternance_R114440-1", "externalId" : "R114440", "industryFunction" : { }, "locationPoint" : "46.2276,2.2137", "structuredLocations" : [ { "country" : "France", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "France", "employmentType" : "FULL_TIME", "coreResponsibilities" : "Assist in marketing campaigns, Support communication actions, Contribute to content creation, Help organize events, Participate in audience analysis, Assist in reporting", "teamCollaboration" : "Marketing team; Communication team; Audience strategy team", "domainKnowledge" : "Audience strategy", "domainList" : [ "audience-strategy" ], "domainSpecificKnowledge" : [ "Audience strategy" ], "communicationSkills" : "Content creation; Reporting", "continuousLearning" : "Learning opportunities", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "[_RX France_](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Frxglobal.com%2Frx-france&data=05%7C02%7CFrederique.LEBRIS%40rxglobal.com%7C62820a5b8ff342ef640d08debcabe938%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C639155643782295059%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=Xthpku77iytgJ85OZCjA7nqAqzifJ1OVgOg6zZ5aOIk%3D&reserved=0) est créateur de places de rencontres à forte valeur ajoutée, leader sur une quinzaine de marchés différents. Parmi les salons emblématiques de RX France et incontournables sur le plan national et international, figurent MIPIM, MAPIC, Batimat, Pollutec, EquipHotel, SITL, IFTM, Big Data & AI Paris, MIPCOM, Paris Photo et bien d’autres… Nos événements se déroulent en France, à Hong Kong, en Italie et au Mexique. Pour plus d'informations sur [_www.rxglobal.fr_](https://nam11.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.rxglobal.fr%2F&data=05%7C02%7CFrederique.LEBRIS%40rxglobal.com%7C62820a5b8ff342ef640d08debcabe938%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C639155643782317930%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=OREbh%2BpbrN5WZ47UXvhq4qFcVr0Z%2FeU%2Fh2qhXQzRgSc%3D&reserved=0) RX France recherche activement un(e) **Assistant/Assistante marketing et communication en Alternance** pour rejoindre les équipes marketing du pôle Audiences Stratégiques. ** _Description du poste_** Au sein des équipes marketing, vous participerez au suivi du plan marketing de chaque salon sur les thématiques suivantes : **Marketing :** Réflexion et création contenu newsletters partenaires Mise à jour et création de documents Veille marché Sur site, accueil des partenaires, gestion de visites guidées, création des badges, service client onsite exposants et visiteurs etc. **Communication :** Site internet : mise à jour et optimisation des contenus du site internet Plan marketing relationnel : création des emails suivant la charte établie et les contenus donnés Réseaux Sociaux : accompagnement pour la récupération des contenus auprès des équipes en interne et des partenaires Outils de communication : être le garant de la bonne mise en œuvre des différents outils de com vendus et deals de partenariats Accompagnement sur site pour la gestion des prestataires (photos, vidéos, RS, agence de presse, hôtesses) ** _Profil_** Vous êtes organisé, rigoureux et autonome. Vous avez une appétence pour le digital. Vous êtes polyvalent, avez le sens du service et du client ainsi que le goût pour le travail en équipe. Votre anglais est courant. **_Qui sommes-nous_** __ : Chez RX France, nous sommes passionnés par l'idée d'avoir un impact positif sur la société et nos clients grâce à la puissance de la rencontre. Nous créons des places de rencontres à très haute valeur ajoutée pour 15 secteurs d’activité, à travers des salons emblématiques tels que MIPIM, Mondial du Bâtiment, Pollutec, MIPCOM, Paris Photo, et bien d'autres. En rejoignant RX France, vous ferez partie d'une entreprise qui valorise la diversité et l'inclusion. Nous nous engageons à créer un environnement de travail juste et équitable pour nos collaborateurs, indépendamment de leur sexe, de leur identité sexuelle, de leur origine, de leur religion, de leur orientation sexuelle, de leur âge ou de leur handicap. Tous nos postes sont ouverts aux personnes en situation de handicap et nous sommes prêts à mettre en place des aménagements pour faciliter le processus de recrutement. De plus, toutes les personnes, indépendamment de leur genre, recevront un traitement équitable en matière de rémunération. Rejoignez-nous chez RX France et contribuez à notre mission d'offrir une expérience magique et impactante à nos clients, en multipliant leurs opportunités de business. Primary Location Base Pay Range: FRANCE - Tour Vista €13 900 - €23 400. **We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. Click**[** _here_**](https://www.relx.com/careers/join-us/benefits)**to access benefits specific to your location.** We are committed to providing a fair and accessible hiring process. If you have a disability or other need that requires accommodation or adjustment, please let us know by completing our [Applicant Request Support Form](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fforms.office.com%2Fr%2FeVgFxjLmAK&data=05%7C02%7CSharon.Martin%40lexisnexis.com%7C2104edc7df90474aaf1108dd8cccf948%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C638821534169028029%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=2Dm7y%2B%2Flckb5oqa13cjE0WAV1kG%2BuqVQDi4dpvwoM5E%3D&reserved=0) or please contact 1-855-833-5120. **Criminals may pose as recruiters asking for money or personal information. We never request money or banking details from job applicants. Learn more about spotting and avoiding scams**[**here**](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fstories.relx.com%2Fhow-to-avoid-job-scams%2Findex.html&data=05%7C02%7CSharon.Martin%40lexisnexis.com%7C2104edc7df90474aaf1108dd8cccf948%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C638821534169036749%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=bMcV1zP1yRXUuNWYwyGuPPb7lCyTuoA%2BGPT0d5MfO8I%3D&reserved=0)**.** Please read our [Candidate Privacy Policy](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.relx.com%2Fcareers%2Fjoin-us%2Fprivacy&data=05%7C02%7CSharon.Martin%40lexisnexis.com%7C2104edc7df90474aaf1108dd8cccf948%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C638821534169045885%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=X%2BrqkisseFh6q%2BEqRLuRvCa2dfT9Q2QeATdfGRVQxnI%3D&reserved=0). We are an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law. _**USA Job Seekers:**_ [EEO Know Your Rights](https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.eeoc.gov%2Fsites%2Fdefault%2Ffiles%2F2023-06%2F22-088_EEOC_KnowYourRights6.12.pdf&data=05%7C02%7CSharon.Martin%40lexisnexis.com%7C2104edc7df90474aaf1108dd8cccf948%7C9274ee3f94254109a27f9fb15c10675d%7C0%7C0%7C638821534169055021%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=mEoTzyFpKtgiRgZnquZyELr%2FkuMrW4%2F9zYB4HMS4hdI%3D&reserved=0).", "summaryDescription" : "Assistant/Assistante marketing et communication - Pôle Audiences Stratégiques - Alternance at RX France. Assist in marketing campaigns. 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Oral communication", "documentationSkills" : "Protocol preparation; Informed consent preparation; Monitoring plans development; CRFs completion; TMF maintenance; Clinical report preparation; Completion guidelines; Data listings; Study reports", "problemSolvingSkills" : "Identify problems; Identify solutions", "specialRequirements" : "Post offer criminal background check", "outcomesObjectives" : "Ensure study timelines met; Ensure study costs met; Ensure quality metrics met; Ensure compliance protocol; Ensure compliance SOPs; Ensure compliance regulatory requirements; Ensure vendor compliance; Ensure execution project deliverables", "qualificationsBasic" : "Bachelor's degree life sciences, 8 years clinical research, 4 years managing clinical trials, 4-7 years supporting clinical trials, HIPAA/PHI privacy training, Human Subjects Protection training, GCP training", "qualificationsPreferred" : "Advanced degree, Managing CROs experience", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "POSITION SUMMARY: The Manager, Clinical Trials will be responsible for managing all aspects of clinical trials from start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects of the trials independently, and is expected to provide functional expertise to ensure that study timelines, costs and quality metrics are met and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements. PRIMARY RESPONSIBILITIES: Manage the execution and conduct of all aspects of very complex clinical studies to ensure that timelines, cost, and quality metrics are met Responsible for selection of vendors/CROs and provide effective ongoing management to vendors/CROs working on the project to ensure compliance and execution of project deliverables within the approved budget, study timeline, and study protocol. Works closely with investigative site personnel, CROs, and other study vendors Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites Lead study-related activities such as protocol and informed consent preparation, investigator selection, study training material development and delivery, monitoring plans development and execution, CRFs, design and completion, TMF maintenance, protocol amendment and clinical report preparation, as required Collaborate with Clinical Data Management group to ensure correct CRFs content is collected, prepare comprehensive completion guidelines, and design effective data listings and study reports Train CROs, vendors, investigators and study coordinators on implementation of study protocol Hire, train, manage and oversee Clinical trial staff, and serve as a resource for others within the company for clinical trials management expertise Monitor and track clinical trial progress and provide status update to stakeholders Support sample management and prospective sample testing for studies where Natera functions as a central testing facility Partner with other research and development groups to create a culture of mutual respect and focus on delivery of high-quality project results Develop Clinical Department SOPs and participate in audits as needed This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job. Employee must provide records of current training or complete training relating to HIPAA/PHI privacy, Human Subjects Protection, and GCP training. Must maintain a current status on Natera training requirements including General Policies and Procedure Compliance and security training. Employee must pass post offer criminal background check QUALIFICATIONS: Bachelor’s degree in life sciences, or other relevant discipline required, Advanced degree preferred. 8 years of clinical research experience, including at least 4 years of experience in managing clinical trials as a leading role. 4-7 years of experience in supporting clinical trials in a regulated environment . Experience in managing CROs is preferred. KNOWLEDGE, SKILLS, AND ABILITIES: Knowledge and understanding of Clinical Trial SOPs, FDA Regulations, and ICH-GCPs governing the conduct of clinical trials Demonstrated analytical skills and ability to identify problems and solutions independently Ability to collaborate with the study team, cross functional team members and external collaborators Proficiency in MS Word, Excel and PowerPoint Good organization and planning skills Strong interpersonal skills and communication skills (both written and oral) Strong leadership skills, self-motivated, adaptable to a dynamic and fast paced environment Must have excellent organizational and time management skills. Ability to prioritize and handle multiple tasks and projects in a fast-paced environment The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations. Remote USA $115,800—$144,700 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management. WHAT WE OFFER Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program! For more information, visit www.natera.com. Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide. All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws. If you are based in California, we encourage you to read this important information for California residents. Link: https://www.natera.com/notice-of-data-collection-california-residents/ Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes. For more information: - BBB announcement on job scams - FBI Cyber Crime resource page", "summaryDescription" : "Manager, Clinical Trials at Natera. Skills: Clinical trials management, Regulatory requirements, Vendor management. Manage clinical trials execution. 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"frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Clinical Study Coordinator in Chicago, USA, adjusted for mid-seniority and full-time employment in the healthcare industry." }, "location" : "South Cook/Will County, Chicago, Illinois, United States", "locations" : [ "South Cook/Will County, Chicago", "Illinois", "United States" ], "certifications" : [ "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization" ], "timestamp" : "2026-06-16T13:21:50.873", "fingerprint" : "b7170833b4223279c19879a9283ea28c5f24522062c7ea8ef1b518fbe9ae4b89", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000132293919-clinical-study-coordinator-", "externalId" : "744000132293919", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chicago", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.8755616,-87.6244212" } ], "locationText" : "Chicago, Illinois, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Study conduct tasks", "Data entry", "Monitoring visits", "Mentoring staff", "Administrative tasks", "Patient recruitment", "Patient identification", "Informed consent", "Laboratory testing", "Investigational products", "Clinical supplies", "Temperature monitoring", "Contract negotiations", "Budget negotiations", "Investigator payments", "Staff training", "Study documents", "Regulatory documents", "Site improvements" ], "hardSkillsList" : [ "Protocol adherence", "Data query resolution", "Adverse event reporting", "Protocol deviation reporting", "Investigational product handling", "Site SOP adherence", "Regulatory agency inspections" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Protocol adherence", "level" : "intermediate" }, { "name" : "Data query resolution", "level" : "intermediate" }, { "name" : "Adverse event reporting", "level" : "intermediate" }, { "name" : "Protocol deviation reporting", "level" : "intermediate" }, { "name" : "Investigational product handling", "level" : "intermediate" }, { "name" : "Site SOP adherence", "level" : "intermediate" }, { "name" : "Regulatory agency inspections", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Clinical trial coordination, Site support, Regulatory compliance", "majorSkillsList" : [ "Clinical trial coordination", "Site support", "Regulatory compliance" ], "coreResponsibilities" : "Support medical institution in clinical trial activities, Assess feasibility of clinical studies, Conduct research-related visits, Assist with logistics of scheduling research visits, Assist with testing per schedule of events, Collaborate with ancillary departments, Assist with data entry into EDC systems, Contact CRO or sponsor representatives, Schedule monitoring visits, Resolve study specific issues, Mentor staff, Perform administrative tasks, Act as communication line, Facilitate evaluation of proposed studies, Provide responses to feasibility questions, Participate in patient recruitment/identification, Confirm eligibility for study inclusion, Assist with plan development for recruitment tools, Assist with plan development for retention tools, Assist with plan development for source documentation, Assist with plan development for site tools, Assist research team in obtaining informed consent, Obtain required assessments at each visit, Notify investigator of critical values, Obtain laboratory testing, Process laboratory testing, Ship laboratory testing, Assist in scheduling sponsor visits, Assist in preparation for sponsor visits, Assist in scheduling CRO representative visits, Assist in preparation for CRO representative visits, Track patient recruitment, Track patient enrollment, Support medical site team, Ensure enrollment targets are met, Provide updates on study amendments, Ensure accurate data entry, Ensure timely data entry, Resolve data queries, Assist in reporting adverse events, Assist in reporting protocol deviations, Support handling of investigational products, Support accountability of investigational products, Support reconciliation of investigational products, Maintain study blinding, Assist site staff with temperature monitoring, Support contract negotiations, Support budget negotiations, Oversee Investigator/Site Payments, Ensure staff complete training, Complete retraining for protocol changes, Ensure investigator reviews study documents, Ensure investigator signs study documents, Provide guidance on conducting clinical trials, Maintain study documents, Prepare for on-site study visits, Prepare for audits, Prepare for regulatory agency inspections, Prepare and submit regulatory documents, Prepare and submit correspondence to regulatory authorities, Prepare and submit correspondence to institutional review boards, Involved in on-site training of additional staff, Identify areas needing improvement, Develop tools for site improvements, Maintain licensure, Maintain certifications", "teamCollaboration" : "Cross-functional departments; Ancillary departments; CRO representatives; Sponsor representatives; Medical institution staff; Research staff; Site staff; Milestone One Manager", "domainKnowledge" : "Clinical trial conduct; Human subjects research; Local laws and regulations; Federal laws and regulations; Study protocols; Schedule of events; Inclusion and exclusion criteria; Site SOPs; Study-specific lab manuals; Investigational products; Clinical supplies; Study blinding; Regulatory authorities; Institutional review boards (IRBs)", "domainList" : [ "clinical-trial-conduct", "human-subjects-research", "local-laws-and-regulations", "federal-laws-and-regulations", "study-protocols", "schedule-of-events", "inclusion-and-exclusion-criteria", "site-sops", "study-specific-lab-manuals", "investigational-products", "clinical-supplies", "study-blinding", "regulatory-authorities", "institutional-review-boards-irbs" ], "domainSpecificKnowledge" : [ "Clinical trial conduct", "Human subjects research", "Local laws and regulations", "Federal laws and regulations", "Study protocols", "Schedule of events", "Inclusion and exclusion criteria", "Site SOPs", "Study-specific lab manuals", "Investigational products", "Clinical supplies", "Study blinding", "Regulatory authorities", "Institutional review boards (IRBs)" ], "toolProficiency" : [ "EDC systems" ], "communicationSkills" : "Line of communication", "documentationSkills" : "Source documentation; Study documents; Regulatory documents", "innovationCreativity" : "Develop tools to assist with improvements", "problemSolvingSkills" : "Resolve study specific issues; Resolve data queries", "specialRequirements" : "On-site position", "outcomesObjectives" : "Ensure responses to feasibility questions are provided in due time; Ensure enrollment targets are met at the site level; Ensure accurate and timely data entry; Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial; Ensure the investigator reviews and signs study documents appropriately and within a reasonable period", "qualificationsBasic" : "2 years experience coordinating clinical research studies, Current Good Clinical Practice (GCP), International Air Transport Association (IATA), Current Basic Cardiopulmonary Resuscitation (CPR), Phlebotomy certification unless part of active professional licensure (RN or LPN)", "qualificationsPreferred" : "Nephrology experience, Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. Tasks may include activities associated with the assessment of the feasibility of new/potential clinical studies, conducting research-related visits as outlined in the respective protocol, assisting the site with logistics of scheduling research visits and testing per the schedule of events in the protocol, collaboration with ancillary departments involved in the research visit to assist in a smooth patient flow at research visits., general study conduct tasks, assistance with data entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In addition, mentoring staff and administrative tasks as assigned by the Milestone One Manager. In this job you will: * Acts as a constant line of communication between Milestone One, the Sponsor or CRO, and the medical institution. * Facilitates the evaluation of proposed studies and ensures responses to feasibility questions are provided in due time. * Actively participates in patient recruitment/identification and evaluation for study inclusion by confirming eligibility according to the Inclusion and exclusion criteria. * Assists with plan development for new recruitment / retention tools, source documentation and other site tools to enhance quality and time management of research staff. * Assists the local research team in obtaining informed consent before study entry or any study-related procedures or tests being performed. * Assist with obtaining the required assessments at each visit per the protocol and notify the investigator of any critical values that need immediate attention or would prohibit or delay study treatment. * Assist with obtaining local and central laboratory testing, processing, and shipping per site SOP and study-specific lab manual. * Assist in scheduling and preparation for all types of sponsors or CRO representative visits at the medical institution. * Track patient recruitment and enrollment and actively supports the medical site team to ensure enrollment targets are met at the site level. Provides regular updates to the staff and investigators regarding study amendments. * Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to guidelines and investigator instructions. * Support proper handling, accountability, and reconciliation of all investigational products and clinical supplies. If applicable, always maintain the study blinding. Protocol and sponsor/CRO guidance will be followed if a study participant requires unblinding. * Assist site staff with maintaining appropriate temperature monitoring for study products and supplies. * Support the contract and budget negotiations and oversees Investigator/Site Payments. * Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial. Retraining will be completed for changes to the protocol before site implementation. * Be responsible for ensuring the investigator reviews and signs study documents appropriately and within a reasonable period. Guidance should be provided to educate the site research team on requirements for conducting clinical trials, date format, etc. * Actively participate in maintaining study documents at the medical institution in preparation for on-site study visits/audits or regulatory agency inspections. * Assist with preparing and submitting regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs). * May be involved in the on-site training of additional staff as part of the SEO or other education programs. * Assist with identifying areas that need improvement for specific sites and assists with developing tools to assist with improvements. * Maintain all licensure and certifications applicable to the role of SEO site/Study coordinator II. * SEO SC is responsible for only performing assigned tasks within their training and licensure if applicable. SEO SC should immediately consult the assigned Milestone One manager for tasks that do not fall within their scope. ## Qualifications Education Relevant education and at least two years of experience coordinating clinical research studies involving human subjects OR, if allowed by local regulations, on-the-job training with at least two years of experience coordinating clinical research studies involving human subjects. Nephrology experience preferred. Certifications * Current Good Clinical Practice (GCP) * International Air Transport Association (IATA) * Current Basic Cardiopulmonary Resuscitation (CPR) * Phlebotomy certification unless part of active professional licensure (RN or LPN) * Preferred Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization. May be obtained within (1) year of employment or status change if not currently certified. ## Additional Information Located in South Cook/ Will County, Chicago (On-site position). If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you!", "summaryDescription" : "Clinical Study Coordinator at PSI CRO. Skills: Clinical trial coordination, Site support, Regulatory compliance. Support medical institution in clinical trial activities. Assess feasibility of clinical studies", "postedDate" : "2026-06-15T22:35:56.000", "createdAt" : "2026-06-16T03:37:36.816", "lastUpdated" : "2026-06-16T13:21:50.873", "ingestTimestamp" : "2026-06-16T03:37:36.816", "mongoId" : "6a3091ccf292fd229c0bffdb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Protocol adherence", "Data query resolution", "Adverse event reporting", "Protocol deviation reporting", "Investigational product handling", "Site SOP adherence", "Regulatory agency inspections", "Leadership", "Clinical trial coordination", "Site support", "Regulatory compliance", "Study conduct tasks", "Data entry", "Monitoring visits", "Mentoring staff", "Administrative tasks", "Patient recruitment", "Patient identification", "Informed consent", "Laboratory testing", "Investigational products", "Clinical supplies", "Temperature monitoring", "Contract negotiations", "Budget negotiations", "Investigator payments", "Staff training", "Study documents", "Regulatory documents", "Site improvements", "Clinical trial conduct", "Human subjects research", "Local laws and regulations", "Federal laws and regulations", "Study protocols", "Schedule of events", "Inclusion and exclusion criteria", "Site SOPs", "Study-specific lab manuals", "Study blinding", "Regulatory authorities", "Institutional review boards (IRBs)", "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "EDC systems" ], "skillCount" : 48, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "_score" : 593.5049, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3073e2f292fd229c0043ba", "title" : "Junior Trial Attorney", "company" : "Abramson Labor Group", "industry" : "Legal Services", "salary" : { "min" : 150000.0, "max" : 200000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Burbank, CA, United States", "locations" : [ "Burbank", "CA", "United States" ], "certifications" : [ "Bar Admission" ], "timestamp" : "2026-06-16T13:34:07.771", "fingerprint" : "d1bf6a5a55a45b1154490f026a9a09b8bd0514427e50b13802db5f5c385c63e6", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/AbramsonLaborGroup/3743990013632006--junior-trial-attorney-hybrid-schedule-", "externalId" : "3743990013632006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Burbank", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "34.1812089,-118.3072010" } ], "locationText" : "Burbank, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Juris Doctor", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Case management", "Legal strategy", "Client advising", "Business generation" ], "hardSkillsList" : [ "Legal research", "Drafting pleadings", "Interviewing witnesses", "Gathering evidence", "Negotiating settlements", "Analyzing documents", "Managing budgets" ], "hardSkills" : [ { "name" : "Legal research", "level" : "intermediate" }, { "name" : "Drafting pleadings", "level" : "intermediate" }, { "name" : "Interviewing witnesses", "level" : "intermediate" }, { "name" : "Gathering evidence", "level" : "intermediate" }, { "name" : "Negotiating settlements", "level" : "intermediate" }, { "name" : "Analyzing documents", "level" : "intermediate" }, { "name" : "Managing budgets", "level" : "intermediate" } ], "majorSkills" : "Trial advocacy, Employment law, Case progression", "majorSkillsList" : [ "Trial advocacy", "Employment law", "Case progression" ], "coreResponsibilities" : "Represent clients in court, Conduct hearings, Participate in arbitrations, Attend mediations, Develop case strategies, Present arguments to judges, Present arguments to juries, Conduct legal research, Draft pleadings, Draft motions, Draft briefs, Interview witnesses, Gather evidence, Prepare for trial, Negotiate settlements, Negotiate plea agreements, Provide legal advice, Guide clients on litigation, Manage support staff, Review employment law documents, Analyze employment law documents, Review contracts, Analyze contracts, Monitor court deadlines, Monitor procedural requirements, Participate in client development, Participate in business generation, Maintain case files, Maintain documentation, Develop litigation budgets, Implement litigation budgets, Coordinate expert witnesses, Coordinate consultants", "teamCollaboration" : "Work with legal teams; Work with paralegals; Work with investigators; Work with litigation associates", "projectManagementSkills" : [ "Case management", "Meet strict deadlines" ], "domainKnowledge" : "Employment law; Workers' compensation; Discrimination law; Harassment law; Wrongful termination; Wage disputes; Workplace injuries; Procedural rules", "domainList" : [ "employment-law", "workers-compensation", "discrimination-law", "harassment-law", "wrongful-termination", "wage-disputes", "workplace-injuries", "procedural-rules" ], "domainSpecificKnowledge" : [ "Employment law", "Workers' compensation", "Discrimination law", "Harassment law", "Wrongful termination", "Wage disputes", "Workplace injuries", "Procedural rules" ], "communicationSkills" : "Present arguments", "documentationSkills" : "Maintain case files; Maintain documentation", "continuousLearning" : "Continuing legal education (CLE)", "problemSolvingSkills" : "Legal analysis", "outcomesObjectives" : "Achieve favorable outcomes", "qualificationsBasic" : "Juris Doctor (J.D.), Licensed to practice law, 2-3 years litigation experience, Trial experience", "qualificationsPreferred" : "Familiarity with procedural rules", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Abramson Labor Group is a leading employment and workers' compensation law firm dedicated to advocating for employees' rights. Based in Burbank, CA, we are determined in representing workers who have faced discrimination, harassment, wrongful termination, wage disputes, and workplace injuries. Our team is committed to providing top-tier legal representation with a client-focused approach, ensuring that every case receives the attention and expertise it deserves. At Abramson Labor Group, we foster a dynamic and collaborative work environment where professionals can grow while making a meaningful impact in the lives of our clients. If you are passionate about employment law and workers' rights, we invite you to join our dedicated team. We are seeking a detail-oriented and motivated individual to join our legal team as a Junior Trial Attorney. The successful candidate will play a pivotal role in managing a docket of employment law cases, ensuring efficient case progression, and achieving favorable outcomes for our clients. Key Responsibilities * Represent clients in court trials, hearings, arbitrations, and mediations. * Develop case strategies and present arguments before judges and juries. * Conduct legal research and draft pleadings, motions, and briefs. * Interview witnesses, gather evidence, and prepare for trial. * Negotiate settlements and plea agreements when appropriate. * Provide legal advice and guidance to clients on litigation matters. * Work collaboratively with legal teams, paralegals, and investigators. * Stay up to date with changes in laws, regulations, and legal precedents. * Manage and supervis support staff. * Review and analyze complex employment law documents and contracts. * Monitor compliance with court deadlines and procedural requirements. * Participate in client development and business generation activities. * Maintain detailed case files and documentation. * Develop and implement litigation budgets. * Coordinate with expert witnesses and consultants. ## Qualifications Education: Juris Doctor (J.D.) from an accredited law school. Bar Admission: Licensed to practice law in the relevant jurisdiction(s). Experience: * 2-3 years of litigation experience * Ideally, the candidate will have trial experience. * Strong background in procedural rules (e.g., Rule 23 of the Federal Rules of Civil Procedure). Skills: * Ability to manage multiple cases and meet strict deadlines. * Project management and ability to work as a team player with litigation associates. ## Additional Information What We Offer: * Competitive salary and performance-based bonuses. * Comprehensive benefits package, including health insurance, retirement plans, and unlimited paid time off (PTO). * Opportunities for professional development and continuing legal education (CLE). * A supportive work environment dedicated to teamwork, integrity, and excellence in client service. Department Civil Litigation Employment Type Full Time Location Burbank, CA Workplace type Hybrid Compensation $150,000 - $200,000 / year commensurate with experience #ZR", "summaryDescription" : "Junior Trial Attorney at Abramson Labor Group. Skills: Trial advocacy, Employment law, Case progression. Represent clients in court. Conduct hearings", "postedDate" : "2026-06-15T21:42:38.000", "createdAt" : "2026-06-16T01:31:18.690", "lastUpdated" : "2026-06-16T13:34:07.771", "ingestTimestamp" : "2026-06-16T01:31:18.690", "mongoId" : "6a3073e2f292fd229c0043ba", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 150000, "salaryAnnualMax" : 200000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Legal research", "Drafting pleadings", "Interviewing witnesses", "Gathering evidence", "Negotiating settlements", "Analyzing documents", "Managing budgets", "Trial advocacy", "Employment law", "Case progression", "Case management", "Legal strategy", "Client advising", "Business generation", "Meet strict deadlines", "Workers' compensation", "Discrimination law", "Harassment law", "Wrongful termination", "Wage disputes", "Workplace injuries", "Procedural rules", "Bar Admission" ], "skillCount" : 23, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 587.03973, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Legal", "llmIndustryConfidence" : 0.98 }, { "id" : "6a3073e2f292fd229c0043bb", "title" : "Junior Trial Attorney", "company" : "Abramson Labor Group", "industry" : "Legal Services", "salary" : { "min" : 180000.0, "max" : 250000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Burbank, CA, United States", "locations" : [ "Burbank", "CA", "United States" ], "certifications" : [ "Bar Admission" ], "timestamp" : "2026-06-16T12:29:23.916", "fingerprint" : "995d0962288904c3c844a8275f64a340c8a370a0f6a2d67f99bcaf5427c8dc4a", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/AbramsonLaborGroup/3743990013631926--junior-trial-attorney-remote-must-reside-in-california", "externalId" : "3743990013631926", "industryFunction" : { }, "structuredLocations" : [ { "state" : "California", "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Juris Doctor", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Case management", "Legal strategy", "Settlement negotiation", "Client advising", "Document review", "Budget development" ], "hardSkillsList" : [ "Legal research", "Pleadings drafting", "Motions drafting", "Briefs drafting", "Witness interviewing", "Evidence gathering", "Trial preparation", "Case file maintenance" ], "hardSkills" : [ { "name" : "Legal research", "level" : "intermediate" }, { "name" : "Pleadings drafting", "level" : "intermediate" }, { "name" : "Motions drafting", "level" : "intermediate" }, { "name" : "Briefs drafting", "level" : "intermediate" }, { "name" : "Witness interviewing", "level" : "intermediate" }, { "name" : "Evidence gathering", "level" : "intermediate" }, { "name" : "Trial preparation", "level" : "intermediate" }, { "name" : "Case file maintenance", "level" : "intermediate" } ], "majorSkills" : "Employment law, Workers' compensation, Litigation, Trial advocacy", "majorSkillsList" : [ "Employment law", "Workers' compensation", "Litigation", "Trial advocacy" ], "coreResponsibilities" : "Represent clients in court, Represent clients in hearings, Represent clients in arbitrations, Represent clients in mediations, Develop case strategies, Present arguments before judges, Present arguments before juries, Conduct legal research, Draft pleadings, Draft motions, Draft briefs, Interview witnesses, Gather evidence, Prepare for trial, Negotiate settlements, Negotiate plea agreements, Provide legal advice to clients, Manage docket of employment law cases, Ensure efficient case progression, Achieve favorable outcomes for clients, Stay up to date with laws, Stay up to date with regulations, Stay up to date with legal precedents, Manage junior attorneys, Supervise junior attorneys, Manage support staff, Supervise support staff, Review employment law documents, Analyze employment law documents, Review employment law contracts, Analyze employment law contracts, Monitor compliance with court deadlines, Monitor compliance with procedural requirements, Participate in client development, Participate in business generation, Maintain detailed case files, Maintain documentation, Develop litigation budgets, Implement litigation budgets, Coordinate with expert witnesses, Coordinate with consultants", "teamCollaboration" : "Work collaboratively with legal teams; Work with paralegals; Work with investigators", "domainKnowledge" : "Employment law; Workers' rights; Discrimination law; Harassment law; Wrongful termination; Wage disputes; Workplace injuries; Procedural rules", "domainList" : [ "employment-law", "workers-rights", "discrimination-law", "harassment-law", "wrongful-termination", "wage-disputes", "workplace-injuries", "procedural-rules" ], "domainSpecificKnowledge" : [ "Employment law", "Workers' rights", "Discrimination law", "Harassment law", "Wrongful termination", "Wage disputes", "Workplace injuries", "Procedural rules" ], "documentationSkills" : "Case file maintenance", "continuousLearning" : "Continuing legal education (CLE)", "outcomesObjectives" : "Achieve favorable outcomes for clients", "qualificationsBasic" : "Juris Doctor (J.D.), Licensed to practice law, 2 years litigation experience, Must reside in California", "qualificationsPreferred" : "Trial experience, Background in procedural rules", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Abramson Labor Group is a leading employment and workers' compensation law firm dedicated to advocating for employees' rights. Based in Burbank, CA, we are determined in representing workers who have faced discrimination, harassment, wrongful termination, wage disputes, and workplace injuries. Our team is committed to providing top-tier legal representation with a client-focused approach, ensuring that every case receives the attention and expertise it deserves. At Abramson Labor Group, we foster a dynamic and collaborative work environment where professionals can grow while making a meaningful impact in the lives of our clients. If you are passionate about employment law and workers' rights, we invite you to join our dedicated team. We are seeking a detail-oriented and motivated individual to join our legal team as a Trial Attorney. The successful candidate will play a pivotal role in managing a docket of employment law cases, ensuring efficient case progression, and achieving favorable outcomes for our clients. Key Responsibilities * Represent clients in court trials, hearings, arbitrations, and mediations. * Develop case strategies and present arguments before judges and juries. * Conduct legal research and draft pleadings, motions, and briefs. * Interview witnesses, gather evidence, and prepare for trial. * Negotiate settlements and plea agreements when appropriate. * Provide legal advice and guidance to clients on litigation matters. * Work collaboratively with legal teams, paralegals, and investigators. * Stay up to date with changes in laws, regulations, and legal precedents. * Manage and supervise junior attorneys and support staff. * Review and analyze complex employment law documents and contracts. * Monitor compliance with court deadlines and procedural requirements. * Participate in client development and business generation activities. * Maintain detailed case files and documentation. * Develop and implement litigation budgets. * Coordinate with expert witnesses and consultants. ## Qualifications Education: Juris Doctor (J.D.) from an accredited law school. Bar Admission: Licensed to practice law in the relevant jurisdiction(s). Experience: * 2 years of litigation experience * Ideally, the candidate will have trial experience. * Strong background in procedural rules (e.g., Rule 23 of the Federal Rules of Civil Procedure). Skills: * Ability to manage multiple cases and meet strict deadlines. * Project management and ability to work as a team player with litigation associates. ## Additional Information What We Offer: * Competitive salary and performance-based bonuses. * Comprehensive benefits package, including health insurance, retirement plans, and unlimited paid time off (PTO). * Opportunities for professional development and continuing legal education (CLE). * A supportive work environment dedicated to teamwork, integrity, and excellence in client service. Department Civil Litigation Employment Type Full Time Location Burbank, CA Workplace type Remote - must reside in California Compensation $180,000 - $250,000 / year commensurate with experience #ZR", "summaryDescription" : "Junior Trial Attorney at Abramson Labor Group. Skills: Employment law, Workers' compensation, Litigation, Trial advocacy. Represent clients in court. Represent clients in hearings", "postedDate" : "2026-06-15T21:41:41.000", "createdAt" : "2026-06-16T01:37:38.511", "lastUpdated" : "2026-06-16T12:29:23.916", "ingestTimestamp" : "2026-06-16T01:37:38.511", "mongoId" : "6a3073e2f292fd229c0043bb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 180000, "salaryAnnualMax" : 250000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Legal research", "Pleadings drafting", "Motions drafting", "Briefs drafting", "Witness interviewing", "Evidence gathering", "Trial preparation", "Case file maintenance", "Employment law", "Workers' compensation", "Litigation", "Trial advocacy", "Case management", "Legal strategy", "Settlement negotiation", "Client advising", "Document review", "Budget development", "Workers' rights", "Discrimination law", "Harassment law", "Wrongful termination", "Wage disputes", "Workplace injuries", "Procedural rules", "Bar Admission" ], "skillCount" : 26, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 585.35974, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Legal", "llmIndustryConfidence" : 0.98 }, { "id" : "6a3073e2f292fd229c0043bc", "title" : "Trial Attorney (Remote)", "company" : "Abramson Labor Group", "industry" : "Legal Services", "salary" : { "min" : 200000.0, "max" : 300000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Burbank, CA, United States", "locations" : [ "Burbank", "CA", "United States" ], "certifications" : [ "Bar Admission" ], "timestamp" : "2026-06-16T14:56:59.023", "fingerprint" : "0ce8d6a04c49daa36901fc19c4973fe8fb961db9fb724a9a0a917e7ce48313ff", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/AbramsonLaborGroup/3743990013631077-trial-attorney-remote-must-reside-in-california", "externalId" : "3743990013631077", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Burbank", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "remote", "geo" : "34.1812089,-118.3072010" } ], "locationText" : "Burbank, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Juris Doctor (J. D. )", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Legal writing", "Legal research", "Analytical skills", "Negotiation", "Oral advocacy", "Project management", "Team leadership" ], "hardSkillsList" : [ "Class action litigation" ], "hardSkills" : [ { "name" : "Class action litigation", "level" : "intermediate" } ], "majorSkills" : "Employment law, Class action litigation, Trial advocacy", "majorSkillsList" : [ "Employment law", "Class action litigation", "Trial advocacy" ], "coreResponsibilities" : "Represent clients in court, Represent clients in hearings, Represent clients in arbitrations, Represent clients in mediations, Develop case strategies, Present arguments before judges, Present arguments before juries, Conduct legal research, Draft pleadings, Draft motions, Draft briefs, Interview witnesses, Gather evidence, Prepare for trial, Negotiate settlements, Negotiate plea agreements, Provide legal advice, Provide guidance to clients, Work collaboratively with legal teams, Work collaboratively with paralegals, Work collaboratively with investigators, Stay up to date with laws, Stay up to date with regulations, Stay up to date with legal precedents, Manage junior attorneys, Supervise junior attorneys, Manage support staff, Supervise support staff, Review employment law documents, Analyze employment law documents, Review employment law contracts, Analyze employment law contracts, Monitor compliance with court deadlines, Monitor compliance with procedural requirements, Participate in client development, Participate in business generation, Maintain detailed case files, Maintain documentation, Develop litigation budgets, Implement litigation budgets, Coordinate with expert witnesses, Coordinate with consultants", "teamCollaboration" : "Legal teams; Paralegals; Investigators; Support staff", "domainKnowledge" : "Employment law; Class actions; Procedural rules; Rule 23; Wage and Hour law", "domainList" : [ "employment-law", "class-actions", "procedural-rules", "rule-23", "wage-and-hour-law" ], "domainSpecificKnowledge" : [ "Employment law", "Class actions", "Procedural rules", "Rule 23", "Wage and Hour law" ], "toolProficiency" : [ "Litigation technology", "Document management tools", "E-discovery platforms", "Legal research databases" ], "communicationSkills" : "Oral advocacy", "documentationSkills" : "Case files documentation", "continuousLearning" : "Continuing legal education", "problemSolvingSkills" : "Analytical skills", "specialRequirements" : "Must reside in California", "outcomesObjectives" : "Achieve favorable outcomes", "qualificationsBasic" : "Juris Doctor (J. D. ), Licensed to practice law, 5+ years litigation experience, Trial experience, Depositions experience, Motions experience, Courtroom advocacy experience, Procedural rules experience, Class action settlements experience, Class certification motions experience", "qualificationsPreferred" : "Experience handling large-scale settlements, Mass tort litigation experience, Consumer protection background, Securities fraud background, Employment law background, Antitrust cases background, Federal court litigation experience, Publication record, Speaking engagements experience", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "At Abramson Labor Group, we're not just committed to defending employee rights—we're passionate about it. Whether you're up against a small business or a corporate giant, our highly skilled team of attorneys and legal professionals are ready to fight for you. Headquartered in vibrant Burbank, California, we focus on exclusively protecting employees throughout the entire state of beautiful California. Our dedicated attorneys, paralegals and legal assistants work tirelessly to secure the justice you deserve in all workplace disputes. We pride ourselves on delivering top-notch solutions with integrity, efficiency, and professionalism. Choose Abramson Labor Group and let us champion your cause with unwavering dedication. We are seeking a detail-oriented and motivated individual to join our legal team as a Trial Attorney (Wage & Hour). The successful candidate will play a pivotal role in managing a docket of employment law cases, ensuring efficient case progression, and achieving favorable outcomes for our clients. Key Responsibilities * Represent clients in court trials, hearings, arbitrations, and mediations. * Develop case strategies and present arguments before judges and juries. * Conduct legal research and draft pleadings, motions, and briefs. * Interview witnesses, gather evidence, and prepare for trial. * Negotiate settlements and plea agreements when appropriate. * Provide legal advice and guidance to clients on litigation matters. * Work collaboratively with legal teams, paralegals, and investigators. * Stay up to date with changes in laws, regulations, and legal precedents. * Manage and supervise junior attorneys and support staff. * Review and analyze complex employment law documents and contracts. * Monitor compliance with court deadlines and procedural requirements. * Participate in client development and business generation activities. * Maintain detailed case files and documentation. * Develop and implement litigation budgets. * Coordinate with expert witnesses and consultants. ## Qualifications Education: Juris Doctor (J.D.) from an accredited law school. Bar Admission: Licensed to practice law in the relevant jurisdiction(s). Experience: * 5+ years of litigation experience, preferably in class actions or complex civil litigation. * Trial experience, including depositions, motions, and courtroom advocacy. * Strong background in procedural rules governing class actions (e.g., Rule 23 of the Federal Rules of Civil Procedure). * Demonstrated experience in managing multi-million dollar class action settlements. * Track record of successful class certification motions. Skills: * Exceptional legal writing, research, and analytical skills. * Strong negotiation and oral advocacy abilities. * Ability to manage multiple cases and meet strict deadlines. * Proficiency in litigation technology and document management tools. * Advanced knowledge of e-discovery platforms and legal research databases. * Superior project management and team leadership capabilities. Preferred Qualifications: * Experience handling large-scale settlements or mass tort litigation. * Background in consumer protection, securities fraud, employment law, or antitrust cases. * Strong network and reputation in the legal community for class action litigation. * Advanced degree in Labor Law, Employment Law, or related field. * Federal court litigation experience. * Publication record in legal journals or speaking engagements at industry conferences. ## Additional Information What We Offer: * Competitive salary and performance-based bonuses. * Comprehensive benefits package, including health insurance, retirement plans, and unlimited paid time off (PTO). * Opportunities for professional development and continuing legal education (CLE). * A supportive work environment dedicated to teamwork, integrity, and excellence in client service. Department Civil Litigation Employment Type Full Time Location Burbank, CA Workplace type Remote Compensation $200,000 - $300,000 / year #ZR", "summaryDescription" : "Trial Attorney (Remote) at Abramson Labor Group. Skills: Employment law, Class action litigation, Trial advocacy. Represent clients in court. 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Works with Principal Investigators; Works with study teams; Coordinate with all relevant groups", "domainKnowledge" : "Clinical trials; HCPCS / CPT codes; Standard of care; Medicare regulations; Medical terminology; Oncology clinical trials", "domainList" : [ "clinical-trials", "hcpcs-cpt-codes", "standard-of-care", "medicare-regulations", "medical-terminology", "oncology-clinical-trials" ], "domainSpecificKnowledge" : [ "Clinical trials", "HCPCS / CPT codes", "Standard of care", "Medicare regulations", "Medical terminology", "Oncology clinical trials" ], "documentationSkills" : "Coverage justifications", "problemSolvingSkills" : "Critical assessment projects", "qualificationsBasic" : "Bachelor's Degree or equivalent, Three years of related budget experience, Working knowledge of clinical trials, Familiarity with HCPCS / CPT codes, Understanding of standard of care, Familiarity with Medicare regulations, Working knowledge of medical terminology", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. Position Summary: Coordinates and develops coverage analyses and budgets for both industry sponsored and non-industry sponsored clinical trials, along with any corresponding amendments. Liaises between external sponsors and COH departments to determine suitable coverage justifications and cost allocations for unique clinical trial procedures. Works with Principal Investigators and study teams to finalize clinical trial budgets and obtain approval of coverage analyses, budget estimates, and/or detailed budgets. Negotiates budgets with clinical trial sponsors to ensure optimal cost efficiency. Tracks data and enters, maintains, and reviews financial data from finalized clinical trial agreements and budgets into the OnCore Clinical Trial Management System (CTMS). As a successful candidate, you will: Coordinate with all relevant groups to draft, finalize and gain approval of coverage analyses and budgets while tracking all appropriate data metrics. This includes documenting qualifying clinical trial status, researching coverage limitations, verifying expected medical necessity, and assigning costs for clinical and non-clinical components of each trial. Must understand the clinical trial and corresponding protocol in order to determine coding and charge determinations. Enter and/or review financial data in OnCore and initiate the sign-off process of the OnCore calendar/financial console. Review protocol amendments for any revisions affecting the coverage analysis and/or budget; update previously documented information. Perform critical assessment projects to confirm funding source and assure that negotiations will be consistent with institutional guidelines. Perform detailed analyses of current coverage analyses or budgets to establish precedent pricing and better drafting and development techniques. Assess comparable nature of projects by factors such as study phase or disease-type to ensure appropriate costing. Analyze new protocols, letters of intent, synopses, etc., received from sponsors, review committees or PI/study teams to determine coverage analysis/budget necessity and/or prioritization in coordination with department leadership. Your qualifications should include: Bachelor’s Degree or equivalent combination of education and experience. Three years of related budget experience working in research administration, a Contract Research Organization, pharma or biotech industry, a medical or clinical practice arena, or health insurance industry. Working knowledge of clinical trials. Familiarity with HCPCS / CPT codes. Understanding of what is standard of care or routine care and what is considered research-related in the context of clinical trials. Familiarity with Medicare regulations, guidelines, policies. Working knowledge of medical terminology specific to oncology clinical trials and general study budgeting techniques and coverage analysis techniques. Additional information: City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. Job Status: Full time, exempt Salary range $ 89,806 - $139,198 City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here . To learn more about our Comprehensive Benefits, please CLICK HERE . US-Nationwide-USA-Remote-US-Remote", "summaryDescription" : "Budget Administrator - Clinical Trials at City of Hope. Skills: Clinical trial budgets, Coverage analysis, Financial data management. 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"llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3084c6f292fd229c07583d", "title" : "Clinical Study Coordinator", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Clinical Study Coordinator in Chicago, adjusted for mid-seniority and full-time employment in the healthcare industry." }, "location" : "South Cook/Will County, Chicago, Illinois, United States", "locations" : [ "South Cook/Will County, Chicago", "Illinois", "United States" ], "certifications" : [ "Current Good Clinical Practice (GCP)", "International Air Transport Association (IATA)", "Current Basic Cardiopulmonary Resuscitation (CPR)", "Phlebotomy certification", "Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization" ], "timestamp" : "2026-06-16T12:57:39.777", "fingerprint" : "f1d00d59c90e88f2ed6c6e95bc5872a78e081a782c7449b87cd5b54d48ad6463", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000132293919-clinical-study-coordinator-", "externalId" : "744000132293919", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chicago", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.8755616,-87.6244212" } ], "locationText" : "Chicago, Illinois, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Study conduct tasks", "Data entry", "Monitoring visits", "Mentoring staff", "Administrative tasks", "Patient recruitment", "Patient identification", "Informed consent", "Laboratory testing", "Investigational products", "Clinical supplies", "Temperature monitoring", "Contract negotiations", "Budget negotiations", "Investigator payments", "Staff training", "Study documents", "Regulatory documents", "Regulatory correspondence", "Site improvements" ], "hardSkillsList" : [ "Protocol adherence", "Data query resolution", "Adverse event reporting", "Protocol deviation reporting", "Investigational product handling", "Site SOP adherence", "Study-specific manual adherence", "Regulatory agency inspections" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Protocol adherence", "level" : "intermediate" }, { "name" : "Data query resolution", "level" : "intermediate" }, { "name" : "Adverse event reporting", "level" : "intermediate" }, { "name" : "Protocol deviation reporting", "level" : "intermediate" }, { "name" : "Investigational product handling", "level" : "intermediate" }, { "name" : "Site SOP adherence", "level" : "intermediate" }, { "name" : "Study-specific manual adherence", "level" : "intermediate" }, { "name" : "Regulatory agency inspections", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Clinical trial coordination, Site support, Regulatory compliance", "majorSkillsList" : [ "Clinical trial coordination", "Site support", "Regulatory compliance" ], "coreResponsibilities" : "Act as communication line, Facilitate study evaluation, Provide feasibility responses, Participate in patient recruitment, Confirm eligibility, Assist with plan development, Assist in obtaining informed consent, Assist with obtaining assessments, Notify investigator of critical values, Assist with laboratory testing, Assist with processing and shipping, Assist in scheduling sponsor visits, Assist in scheduling CRO visits, Track patient recruitment, Track patient enrollment, Support enrollment targets, Provide regular updates, Ensure accurate data entry, Resolve data queries, Assist in reporting adverse events, Assist in reporting protocol deviations, Support handling investigational products, Support accountability of investigational products, Support reconciliation of investigational products, Maintain study blinding, Follow protocol guidance, Follow sponsor guidance, Follow CRO guidance, Assist site staff with temperature monitoring, Support contract negotiations, Support budget negotiations, Oversee Investigator payments, Oversee Site Payments, Ensure staff training completion, Complete retraining for protocol changes, Ensure investigator reviews documents, Ensure investigator signs documents, Provide guidance on requirements, Educate research team, Maintain study documents, Prepare for study visits, Prepare for audits, Prepare for inspections, Prepare regulatory documents, Submit regulatory documents, Submit correspondence to regulatory authorities, Submit correspondence to IRBs, Involve in on-site training, Assist with identifying areas for improvement, Develop tools for improvements, Maintain licensure, Maintain certifications, Perform assigned tasks, Consult manager for out-of-scope tasks", "teamCollaboration" : "Milestone One; Sponsor representatives; CRO representatives; Medical institution; Ancillary departments; Local research team; Site staff", "domainKnowledge" : "Clinical trial conduct; Human subjects research; Local laws; Federal laws; Study protocols; Site SOPs; Study-specific lab manuals; Investigational products; Clinical supplies; Regulatory authorities; Institutional review boards", "domainList" : [ "clinical-trial-conduct", "human-subjects-research", "local-laws", "federal-laws", "study-protocols", "site-sops", "study-specific-lab-manuals", "investigational-products", "clinical-supplies", "regulatory-authorities", "institutional-review-boards" ], "domainSpecificKnowledge" : [ "Clinical trial conduct", "Human subjects research", "Local laws", "Federal laws", "Study protocols", "Site SOPs", "Study-specific lab manuals", "Investigational products", "Clinical supplies", "Regulatory authorities", "Institutional review boards" ], "toolProficiency" : [ "EDC systems" ], "documentationSkills" : "Source documentation; Study documents; Regulatory documents", "problemSolvingSkills" : "Resolve study specific issues; Resolve data queries", "outcomesObjectives" : "Ensure responses provided in due time; Ensure enrollment targets are met; Ensure accurate and timely data entry; Ensure staff training completion; Ensure investigator reviews and signs documents", "qualificationsBasic" : "2 years experience coordinating clinical research studies, Current Good Clinical Practice (GCP), International Air Transport Association (IATA), Current Basic Cardiopulmonary Resuscitation (CPR), Phlebotomy certification unless part of active professional licensure (RN or LPN)", "qualificationsPreferred" : "Nephrology experience, Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. Tasks may include activities associated with the assessment of the feasibility of new/potential clinical studies, conducting research-related visits as outlined in the respective protocol, assisting the site with logistics of scheduling research visits and testing per the schedule of events in the protocol, collaboration with ancillary departments involved in the research visit to assist in a smooth patient flow at research visits., general study conduct tasks, assistance with data entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In addition, mentoring staff and administrative tasks as assigned by the Milestone One Manager. In this job you will: * Acts as a constant line of communication between Milestone One, the Sponsor or CRO, and the medical institution. * Facilitates the evaluation of proposed studies and ensures responses to feasibility questions are provided in due time. * Actively participates in patient recruitment/identification and evaluation for study inclusion by confirming eligibility according to the Inclusion and exclusion criteria. * Assists with plan development for new recruitment / retention tools, source documentation and other site tools to enhance quality and time management of research staff. * Assists the local research team in obtaining informed consent before study entry or any study-related procedures or tests being performed. * Assist with obtaining the required assessments at each visit per the protocol and notify the investigator of any critical values that need immediate attention or would prohibit or delay study treatment. * Assist with obtaining local and central laboratory testing, processing, and shipping per site SOP and study-specific lab manual. * Assist in scheduling and preparation for all types of sponsors or CRO representative visits at the medical institution. * Track patient recruitment and enrollment and actively supports the medical site team to ensure enrollment targets are met at the site level. Provides regular updates to the staff and investigators regarding study amendments. * Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to guidelines and investigator instructions. * Support proper handling, accountability, and reconciliation of all investigational products and clinical supplies. If applicable, always maintain the study blinding. Protocol and sponsor/CRO guidance will be followed if a study participant requires unblinding. * Assist site staff with maintaining appropriate temperature monitoring for study products and supplies. * Support the contract and budget negotiations and oversees Investigator/Site Payments. * Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial. Retraining will be completed for changes to the protocol before site implementation. * Be responsible for ensuring the investigator reviews and signs study documents appropriately and within a reasonable period. Guidance should be provided to educate the site research team on requirements for conducting clinical trials, date format, etc. * Actively participate in maintaining study documents at the medical institution in preparation for on-site study visits/audits or regulatory agency inspections. * Assist with preparing and submitting regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs). * May be involved in the on-site training of additional staff as part of the SEO or other education programs. * Assist with identifying areas that need improvement for specific sites and assists with developing tools to assist with improvements. * Maintain all licensure and certifications applicable to the role of SEO site/Study coordinator II. * SEO SC is responsible for only performing assigned tasks within their training and licensure if applicable. SEO SC should immediately consult the assigned Milestone One manager for tasks that do not fall within their scope. ## Qualifications Education Relevant education and at least two years of experience coordinating clinical research studies involving human subjects OR, if allowed by local regulations, on-the-job training with at least two years of experience coordinating clinical research studies involving human subjects. Nephrology experience preferred. Certifications * Current Good Clinical Practice (GCP) * International Air Transport Association (IATA) * Current Basic Cardiopulmonary Resuscitation (CPR) * Phlebotomy certification unless part of active professional licensure (RN or LPN) * Preferred Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization. May be obtained within (1) year of employment or status change if not currently certified. ## Additional Information Located in South Cook/ Will County, Chicago (On-site position). If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you!", "summaryDescription" : "Clinical Study Coordinator at PSI CRO. Skills: Clinical trial coordination, Site support, Regulatory compliance. Act as communication line. 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Including your own. The Impact You’ll Make Recursion is at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics. We are seeking a highly motivated, skilled, and adaptable Clinical Trial Manager within our Clinical Operations team who will manage the conduct and execution of one or more clinical trials from study start-up to study closure in close collaboration with the Clinical Project Manager and/or Associate Director/Director of Clinical Operations. In this role, you will: Support the Clinical Project Manager in the execution of trial operations across diverse therapeutic areas to deliver transformative, new medicines to patients Manage and track clinical trial activities, timelines, and deliverables Engage and build relationships with clinical CRO and trial partners to support the successful execution of clinical trial activities Proactively identify opportunities for operational and process improvements within the Clinical Operations team Contribute to the advancement of the Recursion development portfolio The Team You’ll Join Reporting to an Associate Director/Director of Clinical Operations, you will be an essential member of the Clinical Operations team within Development and work closely with cross-functional study teams. You will impact all phases of Development clinical trials. The team is dedicated to ensuring operational excellence across our clinical programs. The Experience You’ll Need Bachelor’s degree or equivalent experience 6+ years of experience in a clinical operations role in the biopharmaceutical industry, with at least 2+ years experience as a regional CTM or similar operations role required Preferred experience: monitoring experience, automating trial activity tracking through Smartsheet or other CTMS/tracking tools Early phase (Phase 1, 2) oncology and/or rare disease experience at a Sponsor or CRO is required Strong working knowledge of FDA, ICH, GCP regulations and guidelines Effective collaboration in a fast-paced team environment Excellent interpersonal and communication skills, and an understanding of principles of relationship management across diverse internal and external stakeholders Detail-oriented with effective organizational and problem-solving abilities. Experience in managing multiple priorities and able to accomplish tasks within a timeframe, setting milestones to meet deadlines and to achieve goals Proficient in using various software applications related to clinical trials, such as, but not limited to: smartsheet, clinical trial management systems, project management tools, document management systems, and electronic data capture tools Willingness to travel to sites, conferences, and/or Recursion offices (NYC and SLC) as needed Working Location & Compensation: This position is open to both remote and hybrid models. The hybrid position would be office-based at our London, England office near King's Cross. Employees are expected to work in the office at least 50% of the time. Relocation support can be provided for candidates not local to either geographical location. At Recursion, we believe that every employee should be compensated fairly. Based on the skill and level of experience required for this role, the estimated current annual base range for this role is £62,400 to £84,000. You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package. #LI-ES1 #LI-REMOTE The Values We Hope You Share: We act boldly with integrity. We are unconstrained in our thinking, take calculated risks, and push boundaries, but never at the expense of ethics, science, or trust. We care deeply and engage directly. Caring means holding a deep sense of responsibility and respect - showing up, speaking honestly, and taking action. We learn actively and adapt rapidly. Progress comes from doing. We experiment, test, and refine, embracing iteration over perfection. We move with urgency because patients are waiting. Speed isn’t about rushing but about moving the needle every day. We take ownership and accountability. Through ownership and accountability, we enable trust and autonomy—leaders take accountability for decisive action, and teams own outcomes together. We are One Recursion. True cross-functional collaboration is about trust, clarity, humility, and impact. Through sharing, we can be greater than the sum of our individual capabilities. Our values underpin the employee experience at Recursion. They are the character and personality of the company demonstrated through how we communicate, support one another, spend our time, make decisions, and celebrate collectively. More About Recursion Recursion (NASDAQ: RXRX) is a clinical-stage TechBio company decoding biology to radically improve lives. Recursion is advancing a portfolio of differentiated investigational medicines across its wholly owned and partnered pipeline in oncology, rare disease, neuroscience, immunology, and other therapeutic areas with significant unmet need. Enabling its mission is the Recursion OS, an AI-native, end-to-end drug discovery and development platform integrating biology, chemistry, and clinical development into a unified intelligence system. Powered by proprietary multimodal data, purpose-built AI models, and bilingual teams fluent in both science and AI, the Recursion OS is designed to translate complex science into medicines that matter — faster, better, and at scale — for patients who are waiting. Recursion’s platform infrastructure is anchored in Salt Lake City, Utah and Milton Park, Oxfordshire, where its automated biology and chemistry laboratories generate proprietary data at industrial scale. Recursion also maintains offices in New York, Montréal, and London, three global hubs for talent and leadership at the intersection of AI and scientific innovation. Learn more at www.recursion.com, or connect on X and LinkedIn. Recursion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable federal, state, local, or provincial human rights legislation. Accommodations are available on request for candidates taking part in all aspects of the selection process. Recruitment & Staffing Agencies: Recursion Pharmaceuticals and its affiliate companies do not accept resumes from any source other than candidates. The submission of resumes by recruitment or staffing agencies to Recursion or its employees is strictly prohibited unless contacted directly by Recursion’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Recursion, and Recursion will not owe any referral or other fees. Our team will communicate directly with candidates who are not represented by an agent or intermediary unless otherwise agreed to prior to interviewing for the job.", "summaryDescription" : "Senior Clinical Trial Manager at Recursion. Skills: Clinical trial management, Clinical operations, Regulatory compliance. Support Clinical Project Manager. 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City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. The Senior Budget Administrator coordinates and oversees the development of coverage analyses and budgets for both industry sponsored and non-industry sponsored clinical trials. Works with third party vendors as necessary to supply clinical trial documentation, prioritize work queues, and assist with budget development. Negotiates budgets with clinical trial sponsors on behalf of the institution to ensure optimal cost efficiency. Tracks all relevant data and ensures both contracting and Revenue Integrity teams are supplied with finalized documentation. Enters, maintains and/or reviews financial data from finalized clinical trial agreements and budgets into the OnCore Clinical Trial Management System (CTMS). Provides day-to-day administrative support to Principal Investigators, clinical research nurses, research site managers, clinical research coordinators, departmental business directors and other stakeholders in resolving budget development issues, including but not limited to budget estimates and qualifying trial assessments. Charged with ensuring that incremental costs of clinical research are covered per institutional policies and guidelines while applying clinical research billing compliance expertise pertaining to all applicable payers. The position includes the general development and ongoing refinement of administrative infrastructure for the management of financial activity associated with for-profit corporate sponsorship as well as non-industry submissions pertaining to clinical trials. Provides guidance and serves as the point of contact for new and junior staff, specifically Budget Analysts and Coverage Analysts for financial related questions, engaging management as appropriate. Assist new/junior staff with prioritizing tasks. May provide training, onboarding and/or mentorship to new/junior staff; may have supervisory responsibilities. Ensures quality of the study start-up activities; as needed may conduct quality review and/or audits of clinical trial coverage analysis, budgets, clinical trial agreements and/or financial data entered in OnCore. As a successful candidate, you will: Coordinate with all relevant groups to draft, finalize, and gain approval of coverage analyses and budgets while tracking all appropriate data metrics. Review coding and charge determinations with PI and study team. Enter and/or review financial data in OnCore and initiate the sign-off process of the OnCore calendar/financial console. Perform critical assessment of each project to confirm funding source and negotiates consistently as per institutional guidelines. Perform detailed analyses of current budgets to establish precedent pricing and better budget development techniques. Assess comparable nature of projects by factors such as study phase or disease-type to ensure appropriate costing. Analyze new protocols, letters of intent, synopses, etc., received from sponsors, review committees or PI/study teams to determine coverage analysis/budget necessity and/or prioritization in coordination with department leadership. Interact with sponsor officials to solve budget issues such as budgetary changes, target patient accrual changes, requests for additional funds, or general cost disputes. Compile non-detailed budget estimates via internal estimation tools, as needed and when applicable to sponsor guidelines. Work with third-party vendors if detailed estimates are required Carry out periodic reviews of study files to ensure administrative quality, compliance, and consistency across clinical trials Review protocol amendments for any revisions affecting the budget; updates budget as necessary or re-prioritizes for additional development by a third-party vendor. Your qualifications should include: Bachelor’s Degree or equivalent combination of education and experience. Six years of dedicated experience in oncology clinical research budget development and negotiation and/or coverage analysis development. Experience working in research administration, a Contract Research Organization, pharma, biotech industry, academic medical center, or a clinical practice arena. Experience with HCPCS / CPT codes. Experience with Medicare regulations, guidelines, policies. Preferred education: PharmD, Bachelor of Science in Nursing, or Masters in a health-related field. Additional Information: Job Status: Full time, exempt Salary range $130,977 - $161,219 City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . 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Define, develop, and maintain clinical development strategies across indications, ensuring consistency with the Target Product Profile and overall asset strategy. Oversee end-to-end clinical trial planning and execution, including timelines, budgets, resources, and risk mitigation in collaboration with project management and finance teams. Drive creation and maintenance of the CDP, ensuring endorsement by governance bodies and alignment with strategic objectives and operational feasibility. Lead cross-functional coordination across clinical operations, medical, regulatory, biostatistics, and other stakeholders to ensure integrated execution of clinical programs. Identify, assess, and mitigate program risks, ensuring escalation when needed and driving resolution of complex operational or strategic issues. Oversee vendor and CRO selection and management, ensuring operational quality, compliance, and delivery against expectations. Ensure inspection readiness and compliance with ICH-GCP, SOPs, and applicable global regulatory requirements across all clinical activities. Provide oversight of clinical trial design, feasibility, country/site selection, and protocol development in collaboration with global stakeholders. Contribute to governance meetings, program dashboards, and executive reporting on progress, risks, and financial performance. May provide line management for Clinical Trial Managers and Clinical Trial Associates, including hiring, onboarding, performance management, and development. Support continuous improvement initiatives and promote best practices across clinical operations and development functions. Requirements: Bachelor’s or advanced degree in life sciences, medicine, pharmacy, biomedical sciences, or related field; PhD is a plus. 10+ years of experience in clinical development and/or clinical operations within the pharmaceutical or biotechnology industry, including global trial leadership responsibilities. Strong expertise in clinical trial design, execution, and management across multiple phases, including outsourced models and CRO oversight. Demonstrated experience in developing and executing clinical development strategies and integrated development plans. Strong understanding of ICH-GCP guidelines, global regulatory requirements, and clinical development best practices. Proven ability to manage complex clinical programs, including budgets, timelines, resources, and risk frameworks. Strong leadership, stakeholder management, and cross-functional collaboration skills in a global matrix environment. Excellent communication skills, with the ability to influence, align, and engage senior stakeholders across functions. Strong organizational and analytical skills with the ability to manage competing priorities and complex programs. Experience in rare disease or autoimmune clinical development is a plus. Willingness to operate in a global environment with periodic travel as required. Benefits: Competitive base salary range of $212,000 – $291,500, plus eligibility for short-term and long-term incentive programs. Comprehensive health, dental, vision, life, and disability insurance coverage. Retirement savings plan with employer matching contributions. Generous paid time off and additional well-being support programs. Performance-based incentive opportunities aligned with individual and company success. Exposure to global clinical development strategy across multiple indications and therapeutic areas. High-impact leadership role with visibility at senior governance and executive levels. Opportunity to shape innovative clinical development programs in a fast-growing biotech environment. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Clinical Operations Development Lead. Skills: Clinical operations, Clinical development, Global trial leadership. Co-lead Clinical Development Teams. 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City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. About the Role The Vice President, Clinical Trial Operations (VP CTO) provides strategic, operational, and executive leadership for all clinical research conducted across City of Hope’s national system. This leader oversees systemwide clinical research implementation, standardization, care delivery, workflow optimization, and performance improvement to ensure every patient—regardless of location—has access to high-quality clinical trials. As a successful candidate, you will: Operational Strategy & Leadership Oversee systemwide implementation of standardized workflows, technology integration, and operational processes that support clinical trial growth and excellence. Build strong relationships with internal and external stakeholders, including disease program leaders, PIs, foundation leadership, and sponsors. Guide systemwide strategic planning, goal setting, reporting, and process alignment to support clinical research expansion. Increase clinical research accrual through aligned processes, high-quality operations, and effective communication across the enterprise. Personnel Leadership Recruit, develop, and oversee clinical research personnel systemwide, ensuring adequate staffing, training, licensure, and performance standards. Develop staffing plans and manage performance improvement initiatives for all direct and indirect reports Provide coaching, development, and advancement opportunities for high-performing team members. Clinical Research Execution Establish and maintain systemwide standards for trial execution, patient safety, protocol compliance, and accurate data collection. Ensure strong relationships across clinical research teams and support high-quality patient care. Identify and implement SOPs and quality standards across research operations. Fiscal & Budget Oversight Develop and manage budgets, monitor financial performance, and identify opportunities for improved efficiency and cost savings. Collaborate on new programs and services that support the growth of clinical research across the system. Training, Quality & Performance Improvement Lead the development of systemwide onboarding, training, and continuous education programs for clinical research staff. Develop performance metrics and drive quality improvement initiatives. Ensure adherence to regulatory standards and lead systemwide performance improvement activities. Analyze data, define outcomes, and recommend strategies that improve patient experience and operational efficiency. Clinical Research Care Coordination Oversight Advance a culture of excellence in research practice and ensure seamless coordination of clinical research activity across all COH sites. Align trial openings with population needs and site resources. Build strategic partnerships with investigators, physicians, sponsors, cancer center leadership, and cross-functional departments. Your qualifications should include: Minimum Education Master’s degree in Nursing, Business Management, or related field Minimum Experience 15+ years of oncology clinical research experience , focused on clinical trials operations and patient-centered excellence. 15+ years of clinical trials management experience in an academic setting. Experience leading multidisciplinary clinical research teams. Deep knowledge of FDA regulations, GCP, HIPAA, NCI CCSG guidelines, and clinical research operations.. Preferred Experience Experience with Lean, Six Sigma, PDCA, and performance improvement methodologies. Proven leadership, project management, analytic, and communication skills. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . 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Our unique philosophy of “early identification – early resolution” has earned us decades of trust and respect from our clients. At Carr Allison, our success is fueled by the collective efforts of our team and we believe that an open-door policy is essential to our continued growth. We proudly champion teamwork, collaboration, and the pursuit of excellence as cornerstones of our firm's culture. Join a team where your growth is our priority and your work truly matters. We are seeking a Trial Attorney to join our Orlando team. This attorney will manage a caseload of premises liability and motor vehicle accident cases for corporate clients. The ideal candidate has significant civil litigation experience and has taken an active role in at least two trials. Experience deposing medical or biomechanical experts is highly valued. Responsibilities: Handle a manageable caseload with full autonomy. Draft pleadings, motions, and discovery. Conduct document review and case triage. Engage in trial preparation and take an active role in trials. Depose medical and biomechanical experts as needed. Serve as a key resource and mentor for associates in the Orlando office. Qualifications: Trial experience is required. Bodily injury litigation experience, with auto or premises liability experience preferred. Ability to manage a caseload independently and meet deadlines. Leadership potential and willingness to be a go-to resource for the team. Office Culture: We are a growing office focused on building a collaborative, team-oriented culture. This role offers the opportunity to be a leader within the office and support our efforts to create a strong, connected team. Professional growth and leadership development are core priorities. For more information, please reach out to Smith Busby at sbusby@carrallison.com. Be part of a firm that values your potential and empowers your success.", "summaryDescription" : "Trial Attorney at Carr Allison. 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City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. This full-time remote position entails ensuring data integrity for various research studies. Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data. You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research. As a successful candidate, you will: Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations. Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information. Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution. Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements. Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work. Qualifications - External Qualifications - External Qualifications - External Your qualifications should include: Bachelor’s Degree, relevant experience may substitute for degree. At least two years of experience related to the conduct of oncology clinical trials. Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Clinical Trials Data Coord at City of Hope. Skills: Data science, Data engineering, ML/AI, Business intelligence, Analytics engineering. Ensure data integrity. 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Pawtucket, Rhode Island, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Data compilation", "Data review", "Data analysis", "Clinical trial set-up", "Operational support" ], "hardSkills" : [ { "name" : "Data compilation", "level" : "intermediate" }, { "name" : "Data review", "level" : "intermediate" }, { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Clinical trial set-up", "level" : "intermediate" }, { "name" : "Operational support", "level" : "intermediate" } ], "majorSkills" : "Trial operations leadership, Clinical trial management, Vendor management, Budget oversight", "majorSkillsList" : [ "Trial operations leadership", "Clinical trial management", "Vendor management", "Budget oversight" ], "coreResponsibilities" : "Provide clinical trial management leadership, Collaborate with cross-functional team members, Develop, propose, and manage plans, Lead RFP preparation, Coordinate proposal evaluation, Provide input into selection and contracting, Manage contracted service providers, Lead investigator and site selection, Review and oversee study budgets, Manage study timelines, Manage study metrics, Conduct risk assessments, Develop mitigation strategies, Develop contingency planning, Communicate with internal/external teams, Recognize challenges, Mitigate/resolve challenges, Participate in clinical trial operations, Coordinate clinical trial protocols, Write clinical trial protocols, Review clinical trial protocols, Finalize clinical trial protocols, Coordinate consent forms, Write consent forms, Review consent forms, Finalize consent forms, Coordinate study plans, Write study plans, Review study plans, Finalize study plans, Coordinate safety reviews, Write safety reviews, Review safety reviews, Finalize safety reviews, Coordinate essential regulatory documents, Write essential regulatory documents, Review essential regulatory documents, Finalize essential regulatory documents, Train new staff, Mentor new staff, Share trial conduct best practices, Implement trial conduct best practices, Oversee adherence to regulations", "teamCollaboration" : "Cross-functional team members; Internal/external teams; Multidisciplinary team", "projectManagementSkills" : [ "Project management", "Timeline management", "Budget management", "Milestone delivery" ], "domainKnowledge" : "Clinical trial regulations; ICH/GCP; US regulatory; Canadian regulatory", "domainList" : [ "clinical-trial-regulations", "ich-gcp", "us-regulatory", "canadian-regulatory" ], "domainSpecificKnowledge" : [ "Clinical trial regulations", "ICH/GCP", "US regulatory", "Canadian regulatory" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Clinical trial protocols; Consent forms; Case report forms; Study plans; Safety reviews; Regulatory documents", "continuousLearning" : "Training; Learning & Development; Tuition Assistance", "problemSolvingSkills" : "Risk assessment; Mitigation strategies; Contingency planning", "specialRequirements" : "5-10% travel", "outcomesObjectives" : "Deliver critical milestones on time; Deliver critical milestones within budget", "qualificationsBasic" : "Project management experience, Organizational skills, Ability to work independently, Ability to work collaboratively, Good judgement, Flexibility, Detail oriented", "qualificationsPreferred" : "Previous experience with CTA and IND submissions preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE https://www.nasdaq.com/market-activity/stocks/xene) is a neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization of life-changing therapeutics for patients in need. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team. What We Do: We are advancing an exciting product pipeline https://xenon-pharma.com/pipeline to address indications with high unmet medical need, including epilepsy, depression and pain. Our Phase 3 azetukalner program represents the most advanced, clinically validated potassium channel modulator in late-stage clinical development for multiple indications. In March 2026, we announced positive topline data from our Phase 3 X-TOLE2 study of azetukalner in focal onset seizures (FOS), and we anticipate submitting a New Drug Application to the Food and Drug Administration in the third quarter of 2026. Our Phase 3 epilepsy program also includes a second FOS study, X-TOLE3, which would support regulatory submissions outside the U.S., and the X-ACKT study in primary generalized tonic-clonic seizures, which would support regulatory submissions for an additional epilepsy indication. We also have multiple Phase 3 azetukalner clinical trials underway in major depressive disorder (MDD) and bipolar depression (BPD), based on topline data from our Phase 2 X-NOVA clinical trial. In addition, we are proud of our strong heritage in human genetics, deep understanding of ion channel biology, and expertise in novel chemistries to enable potent, selective ion channel targeting. We continue to advance an early-stage pipeline of novel therapeutic candidates, including Phase 1 studies for XEN1701 (targeting Nav1.7) and XEN1120 (targeting Kv7), which are important pain targets. Backed by a strong balance sheet to support our growth plans, we continue to build a fully integrated, premier neuroscience company with strong discovery, clinical development, corporate, and commercial operations. About the Role: We are seeking a Senior Manager, Trial Operations to join our team. This person may work flexibly across a number of clinical stage trials and projects, acting as a study lead and manager for select clinical trial and be hands-on in data compilation, review and analysis, clinical trial set-up and management, and operational support activities. This is an excellent opportunity for someone with strong organizational skills and the ability to work independently on a variety of tasks and projects. In addition, the successful candidate must have strong project management experience, excellent verbal and written communication, an ability to work collaboratively, demonstrate good judgement, and be flexible and detail oriented. This position reports to the Director, Trial Operations, and will be based out of Boston, MA, USA in our Needham office. We may consider remote locations for exceptional candidates. This is a Hybrid position requiring a minimum of two onsite days per week. RESPONSIBILITIES: - Provide clinical trial management leadership for multiple Phase 3 studies, across therapeutic areas. - Collaborate with cross-functional team members to ensure highly integrated plans and documents for clinical trials. - Develop, propose, and manage plans for assigned studies and activities. - Lead the preparation of Requests for Proposals (RFPs) in collaboration with other internal team members, coordinate the evaluation of proposals and provide input into the selection and contracting of Contract Research Organizations (CRO) and other clinical service providers. - Manage contracted service providers to deliver against the contracts. - Lead the selection of qualified investigators and study sites in collaboration with the Clinical Development team. - Review and oversee study budgets and invoices to ensure vendors are invoicing in accordance with their contracts. - Develop and manage study timeline and study metrics cross-functionally. - Conduct risk assessments, mitigation strategies and contingency planning. - Communicate with internal/external teams to proactively recognize challenges and work cross-functionally on strategies to mitigate/resolve. - Actively participate in all aspects of clinical trial operations, including the coordination, writing, review and/or finalization of clinical trial protocols, consent forms, case report forms, study plans, safety reviews and other essential regulatory documents. - Train and mentor new staff or peer mentorship of new hires. - Actively participates in documentation, sharing and implementation of trial conduct best practices and lessons learned with junior staff. - Oversee adherence to applicable regulations, recognized guidelines, clinical trial protocol, and standards of clinical practice. - Participate in the development and updating of standard operating procedures as required. - Act in accordance with Company policies, including, for example, the Code of Business Conduct and Ethics. - Other duties as assigned. QUALIFICATIONS: - A minimum bachelor’s degree in a scientific discipline and/or other healthcare designation (e.g., RN). - A minimum of 5-8 years clinical project/study management experience within the pharmaceutical and/or biotechnology/biopharmaceutical industry or at a CRO. Job level will be commensurate with experience. - Ability to lead cross-functional team through all activities in the full clinical study life cycle. - Strong vendor management skills and experience managing outsourced work. - A good understanding of all phases of the drug development process and the interdependencies between Clinical and other functional areas (e.g., CMC, nonclinical/toxicology, Regulatory Affairs etc.), with specific experience in phase 3 clinical trials preferred. - Demonstrated ability to successfully work across a variety of teams and manage multiple conflicting priorities. - Demonstrated ability to successfully manage and deliver on critical milestones in the successful completion of clinical trials on time and within budget. - Strong knowledge and understanding of ICH/GCP and US and Canadian regulatory environments; a comprehensive understanding of clinical trial regulations across multiple jurisdictions with previous experience with CTA and IND submissions preferred. - Excellent oral and written communication skills. - Strong interpersonal skills and ability to foster strong collaborative relationships with internal and external team members. - Ability to work both independently and collaboratively as part of a multidisciplinary team. - Exceptional attention to detail and excellent organizational skills. - Ability to thrive in a dynamic and fast-paced environment. - Ability to prioritize duties and manage multiple matters from start to finish with minimal supervision and with a demonstrated ability to lead change and make independent decisions. - Ability to handle highly confidential and sensitive materials and information with complete discretion. - Ability and willingness to travel 5-10% of the time (internationally and domestic) To apply for this position, click Apply Now to complete the application. We thank all applicants for their interest; however, due to the volume of applicants, only those chosen for interview will be contacted. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions. Xenon encourages time to rest and re-charge through vacation, personal days, sick days, and an end-of-year company shutdown. Xenon highly values employee development and has an expanding Training, Learning & Development program, including a Tuition Assistance program for advanced degrees.", "summaryDescription" : "Manager/Senior Manager, Trial Operations at Xenon Pharmaceuticals. Skills: Trial operations leadership, Clinical trial management, Vendor management, Budget oversight. 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Resolve protocol issues, Resolve data discrepancies, Ensure proper documentation, Manage adverse event documentation, Classify adverse events, Follow up on SAEs, Maintain study calendars, Maintain financial triggers, Track data completion, Support monitoring visits, Support study initiation visits, Support audits, Support inspection readiness, Assist with EDC builds, Create data standards, Prepare reports, Participate in CAPA, Participate in process improvement, Mentor peers", "teamCollaboration" : "Working closely with physicians; Working closely with clinical coordinators; Working closely with research teams", "domainKnowledge" : "Oncology clinical trials; First-in-Human studies; Phase IV studies; FDA guidelines; ICH-GCP; ALCOA+; HIPAA; MedDRA; CTCAE; WHO-DDE", "domainList" : [ "oncology-clinical-trials", "first-in-human-studies", "phase-iv-studies", "fda-guidelines", "ich-gcp", "alcoa", "hipaa", "meddra", "ctcae", "who-dde" ], "domainSpecificKnowledge" : [ "Oncology clinical 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City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. The Senior Clinical Trials Data Coordinator supports complex oncology clinical trials from First-in-Human and Phase I through Phase IV by coordinating data collection, entry, quality assurance, and query resolution to ensure accurate, reliable, and compliant research data. The role involves interpreting research protocols, reviewing medical records, resolving discrepancies, and maintaining study visits and financial triggers within the Clinical Trial Management System (CTMS) aligned with Electronic Data Capture (EDC) systems. Working closely with physicians, clinical coordinators, and research teams, the coordinator ensures timely data reporting, supports adverse event data collection, and contributes to study monitoring and regulatory compliance. Additionally, the role includes performing peer data reviews, assisting in the development of data management plans and workflows, and providing training and guidance to research data staff to maintain high-quality clinical trial data and efficient research operations. As a successful candidate, you will: Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. Ensure data accuracy, completeness, and compliance through quality checks, data cleaning, and timely resolution of queries. Maintain regulatory compliance with FDA, ICH-GCP, ALCOA+, HIPAA, and other applicable guidelines for clinical research data management. Collaborate with sponsors, physicians, and clinical coordinators to resolve protocol issues, data discrepancies, and ensure proper documentation. Manage adverse event documentation and classification using standard dictionaries such as MedDRA, CTCAE, and WHO-DDE, including SAE follow-up and query resolution. Maintain study calendars, financial triggers, and data completion tracking in CTMS to support billing and study financial management. Support monitoring visits, study initiation visits, audits, and inspection readiness, ensuring data quality and completeness. Contribute to data management improvements by assisting with EDC builds, creating data standards, preparing reports, participating in CAPA and process improvement initiatives, and mentoring peers. Your qualifications should include: Minimum Education Bachelor’s degree in Science, Health, or a related field from an accredited university, or equivalent relevant work experience. Minimum Experience : Minimum of 5–7 years of clinical research or related experience. Required Certifications: Completion of Good Clinical Practice (GCP) training within 1 month of employment. Completion of Human Subjects Protection (HSP) training within 1 month of employment. Ability to obtain SOCRA or ACRP certification within 2 years of employment. Systems Knowledge: Experience with Clinical Trial Management Systems (CTMS), Electronic Medical Records (EMR), and eRegulatory systems. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here . To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Sr Clinical Trials Data Coord at City of Hope. Skills: Clinical trials, Data management, Regulatory compliance. 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Cross-functional stakeholders; Global, cross-functional teams; External scientific stakeholders", "projectManagementSkills" : [ "Clinical development plans", "Timelines", "Risk mitigation strategies" ], "domainKnowledge" : "Rare kidney disease; Nephrology; Metabolic disease; Genetic disease; Drug development; Regulatory pathways; Pre-IND submissions; NDALA submissions", "domainList" : [ "rare-kidney-disease", "nephrology", "metabolic-disease", "genetic-disease", "drug-development", "regulatory-pathways", "pre-ind-submissions", "ndala-submissions" ], "domainSpecificKnowledge" : [ "Rare kidney disease", "Nephrology", "Metabolic disease", "Genetic disease", "Drug development", "Regulatory pathways", "Pre-IND submissions", "NDALA submissions" ], "communicationSkills" : "Clear communication; Scientific discussions; Medical communications; Presentation skills; Interpersonal skills; Executive presentations", "documentationSkills" : "Clinical documentation; Regulatory filings", "continuousLearning" : "Professional development; Leadership growth opportunities", "problemSolvingSkills" : "Data-driven decision making", "specialRequirements" : "Willingness to travel internationally and domestically up to approximately 25–30%", "qualificationsBasic" : "Medical degree (MD or MD/PhD required), 12+ years clinical research experience, 8+ years leadership experience, Expertise in clinical development strategy, Deep understanding of rare disease drug development, Proven ability to design, interpret, and communicate complex clinical and scientific data, Leadership and influencing skills, Experience collaborating with regulatory agencies, investigators, and key opinion leaders, Ability to manage complexity, prioritize effectively, and adapt", "qualificationsPreferred" : "Nephrology training strongly preferred, NDALA experience preferred", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Serve as Global Development Physician Lead for assigned rare kidney disease programs, overseeing clinical, scientific, and strategic direction across Phases 1–4. Lead the development of clinical trial protocols, study designs, and integrated clinical development strategies aligned with regulatory pathways from pre-IND through NDA/BLA submissions. Represent clinical development programs to executive leadership, governance bodies, and cross-functional program teams, ensuring clear communication of goals, risks, and strategic decisions. Partner with cross-functional stakeholders (Biometrics, Regulatory, Medical Affairs, and Safety) to develop and execute clinical development plans, timelines, and risk mitigation strategies. Oversee interpretation and integration of clinical data, including efficacy, safety, and benefit-risk assessments, to support regulatory filings and program decisions. Engage with regulatory authorities and key opinion leaders to support clinical strategy, study design alignment, and scientific discussions across development stages. Provide clinical and scientific input into publications, presentations, and medical communications in collaboration with Medical Affairs. Lead and mentor clinical development teams and consultants, fostering a high-performance, collaborative, and scientifically rigorous environment. Contribute to alliance and external partner engagement, ensuring alignment on clinical strategy and execution priorities. Support governance processes by presenting program updates, risks, and strategic recommendations to senior leadership forums. Requirements: Medical degree (MD or MD/PhD required); nephrology training strongly preferred. 12+ years of clinical research experience within pharmaceutical or biotech environments, including design and execution of clinical trials across multiple phases. 8+ years of leadership experience managing cross-functional clinical development teams in a matrixed organization. Strong expertise in clinical development strategy, including late-stage programs and regulatory submissions (NDA/BLA experience preferred). Deep understanding of rare disease drug development, ideally within nephrology or metabolic/genetic disease areas. Proven ability to design, interpret, and communicate complex clinical and scientific data. Strong leadership and influencing skills with experience driving alignment across global, cross-functional teams. Excellent communication, presentation, and interpersonal skills, with the ability to engage both internal executives and external scientific stakeholders. Experience collaborating with regulatory agencies, investigators, and key opinion leaders. Ability to manage complexity, prioritize effectively, and adapt in a fast-changing development environment. Willingness to travel internationally and domestically up to approximately 25–30%. Benefits: Competitive executive compensation package including base salary, annual incentive bonus, and long-term equity awards. Comprehensive healthcare coverage including medical, dental, and vision insurance for employees and eligible dependents. Retirement savings plan with employer matching contributions. Generous paid time off and flexible work-life balance policies. Life, disability, and financial protection benefits. Employee wellness programs and support resources. Opportunity to lead high-impact clinical programs in rare disease drug development. Strong professional development and leadership growth opportunities within a global biopharmaceutical environment. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Vice President, Clinical Development. Skills: Clinical Development, Regulatory Pathways, Clinical Trial Leadership. Serve as Global Development Physician Lead. 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Startup en pleine croissance dans le secteur du service à domicile, Ouihelp rassemble déjà plus de 2 500 auxiliaires de vie en France, et nous continuons à grandir avec vous. Chez Ouihelp, nous pensons que prendre soin des autres commence par prendre soin de vous. \uD83D\uDCCD Lieu : Secteur Nancy et alentours \uD83D\uDCC4 Contrat : CDI mandataire – Temps partiel / temps plein ⏱️ Nombre d’heures à pourvoir : entre 5 h et 35 h par semaine, selon vos disponibilités \uD83D\uDCB0 Salaire : À partir de 14,61 € brut/h + avantages \uD83D\uDCBC Votre quotidien chez Ouihelp : Proche de vous… et de chez vous Missions locales, proches de votre domicile Aucun déplacement inutile : nous garantissons aucune mission de moins d’1h Planning stable d’une semaine à l’autre, adapté à vos souhaits en termes d’heures et de jours travaillés Bénéficiaires fixes Des missions qui ont du sens Accompagnement dans les gestes essentiels (toilettes, repas, aide aux courses, ménage,…) Moments de compagnie et de lien social Missions en relation avec les familles pour une relation de confiance durable Un accompagnement sur mesure Prise de poste personnalisée (accompagnement lors de votre 1ère intervention et suivi d’intégration pendant 3 mois) Une équipe OUIHELP réactive pour répondre à vos questions au quotidien, dont une astreinte à votre écoute les week-ends Une application simple et dédiée pour faciliter votre quotidien et vos démarches (Ouihelp Pro) ✅ Les conditions que nous vous offrons : 13,28 € brut/h hors congés payés (soit 14,61 € brut/h congés payés inclus), évolutif selon expérience Majoration attractive : nuits, dimanches, jours fériés et dans le cadre de missions de remplacement Indemnités de trajet (1 € à 2,50 € par nombre d'interventions réalisées) prises en charge Salaire à la demande : possibilité de réaliser des acomptes jusqu’à 50 % en cours de mois Primes de cooptation (d’un montant de 200 €) Partenariat avec AXA (tarifs préférentiels mutuelle santé) Programme de formation continue pour faire évoluer votre carrière Possibilité d’intégrer une formation rémunérée si vous avez 18 mois d’expérience \uD83D\uDC64 Votre profil : Vous êtes diplômé·e du secteur médico-social (DEAES, ADVF, SAPAT, ASSP…) OU vous avez 3 ans d’expérience auprès de personnes âgées Vous avez au moins 18 mois d’expérience ? → Nous vous proposons une formation interne rémunérée dès votre arrivée Poste ouvert à tous, handi-accueillant, permis B NECESSAIRE \uD83E\uDD1D\uD83C\uDFFB Le processus de recrutement : 1️⃣ Un premier échange téléphonique avec la chargée RH 2️⃣ Un entretien physique / visio avec la chargée RH ou le/la responsable de secteur, en fonction des disponibilités de chacun 3️⃣ Contrôle de référence(s) auprès de vos anciens employeurs \uD83D\uDC9A Ouihelp prend soin de ceux qui prennent soin. \uD83D\uDC49\uD83C\uDFFB Rejoignez une entreprise qui vous respecte, vous forme, et vous accompagne au quotidien. \uD83D\uDCE9 Intéressé(e) ? Postulez dès maintenant ! INDNAN1 Salaire horaire pour les AVS / ADV Echelle salariale €14,61—€15,40 EUR", "summaryDescription" : "Assistante de vie H/F at Ouihelp. Skills: Accompagnement personnes âgées. Accompagnement dans les gestes essentiels. 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Collaborate with clinical coordinators; Collaborate with research teams; Collaborate with sponsors", "domainKnowledge" : "Oncology clinical trials; Clinical research data management; FDA guidelines; ICH-GCP guidelines; ALCOA+; HIPAA; MedDRA; CTCAE; WHO-DDE", "domainList" : [ "oncology-clinical-trials", "clinical-research-data-management", "fda-guidelines", "ich-gcp-guidelines", "alcoa", "hipaa", "meddra", "ctcae", "who-dde" ], "domainSpecificKnowledge" : [ "Oncology clinical trials", "Clinical research data management", "FDA guidelines", "ICH-GCP guidelines", "ALCOA+", "HIPAA", "MedDRA", "CTCAE", "WHO-DDE" ], "toolProficiency" : [ "OnCore" ], "documentationSkills" : "Data management plans; Study documentation", "problemSolvingSkills" : "Query resolution; Discrepancy resolution", "outcomesObjectives" : "Ensure accurate, reliable, and compliant research data; Maintain high-quality clinical trial data; Ensure efficient research operations", "qualificationsBasic" : "Bachelor's degree in Science, 5-7 years clinical research experience, GCP training completion, Human Subjects Protection training", "qualificationsPreferred" : "Ability to obtain SOCRA certification, Ability to obtain ACRP certification", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. The Senior Clinical Trials Data Coordinator supports complex oncology clinical trials from First-in-Human and Phase I through Phase IV by coordinating data collection, entry, quality assurance, and query resolution to ensure accurate, reliable, and compliant research data. The role involves interpreting research protocols, reviewing medical records, resolving discrepancies, and maintaining study visits and financial triggers within the Clinical Trial Management System (CTMS) aligned with Electronic Data Capture (EDC) systems. Working closely with physicians, clinical coordinators, and research teams, the coordinator ensures timely data reporting, supports adverse event data collection, and contributes to study monitoring and regulatory compliance. Additionally, the role includes performing peer data reviews, assisting in the development of data management plans and workflows, and providing training and guidance to research data staff to maintain high-quality clinical trial data and efficient research operations. As a successful candidate, you will: Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. Ensure data accuracy, completeness, and compliance through quality checks, data cleaning, and timely resolution of queries. Maintain regulatory compliance with FDA, ICH-GCP, ALCOA+, HIPAA, and other applicable guidelines for clinical research data management. Collaborate with sponsors, physicians, and clinical coordinators to resolve protocol issues, data discrepancies, and ensure proper documentation. Manage adverse event documentation and classification using standard dictionaries such as MedDRA, CTCAE, and WHO-DDE, including SAE follow-up and query resolution. Maintain study calendars, financial triggers, and data completion tracking in CTMS to support billing and study financial management. Support monitoring visits, study initiation visits, audits, and inspection readiness, ensuring data quality and completeness. Contribute to data management improvements by assisting with EDC builds, creating data standards, preparing reports, participating in CAPA and process improvement initiatives, and mentoring peers. Qualifications - External Your qualifications should include: Minimum Education Bachelor’s degree in Science, Health, or a related field from an accredited university, or equivalent relevant work experience. Minimum Experience : Minimum of 5–7 years of clinical research or related experience. Required Certifications: Completion of Good Clinical Practice (GCP) training within 1 month of employment. Completion of Human Subjects Protection (HSP) training within 1 month of employment. Ability to obtain SOCRA or ACRP certification within 2 years of employment. Systems Knowledge: Experience with Clinical Trial Management Systems (CTMS), Electronic Medical Records (EMR), and eRegulatory systems. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here . To learn more about our Comprehensive Benefits, please CLICK HERE . US-Nationwide-USA-Remote-US-Remote", "summaryDescription" : "Sr Clinical Trials Data Coord at City of Hope. Skills: Clinical trial data, Data quality, Regulatory compliance. 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City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. This full-time remote position entails ensuring data integrity for various research studies. Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data. You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research. As a successful candidate, you will: Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations. Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information. Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution. Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements. Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work. Qualifications - External Qualifications - External Qualifications - External Your qualifications should include: Bachelor’s Degree, relevant experience may substitute for degree. At least two years of experience related to the conduct of oncology clinical trials. Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Clinical Trials Data Coord at City of Hope. Skills: Data science, Data engineering, ML/AI, Business intelligence, Analytics engineering. Ensure data integrity. 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Clinical operations leadership; Data management", "projectManagementSkills" : [ "Timeline management", "Action item tracking" ], "domainKnowledge" : "Clinical trial processes; Oncology; Immunology; Respiratory", "domainList" : [ "clinical-trial-processes", "oncology", "immunology", "respiratory" ], "domainSpecificKnowledge" : [ "Clinical trial processes", "Oncology", "Immunology", "Respiratory" ], "toolProficiency" : [ "CTMS platforms", "EDC platforms", "eTMF platforms" ], "communicationSkills" : "Escalate issues", "documentationSkills" : "Study documents; TMF entries; Regulatory documents; Meeting minutes", "specialRequirements" : "Travel up to 20%", "qualificationsBasic" : "6+ years of experience in clinical operations, Foundational understanding of GCP, Foundational understanding of ICH guidelines, Foundational understanding of clinical trial processes, Experience working with or alongside CROs, Experience working with or alongside clinical vendors, Ability to manage multiple trackers, Ability to manage multiple timelines, Ability to manage multiple action items", "qualificationsPreferred" : "Bachelor’s degree scientific preferred, Bachelor’s degree health-related field preferred, Clinical research sponsor-side experience, Familiarity with oncology therapeutic areas, Familiarity with immunology therapeutic areas, Familiarity with respiratory therapeutic areas", "rawDescription" : "The Role: Generate Biomedicines is seeking an organized and proactive Clinical Trial Manager (CTM) to support the operational execution of late-stage clinical trials within our Clinical Development team. This role will report to the Director, Clinical Operations and will serve as a key day-to-day operational coordinator across assigned studies. At Generate Biomedicines, clinical execution is carried out through a network of CROs and specialized vendors. The CTM plays a critical role in ensuring that these external partners stay on track monitoring deliverables, flagging issues, coordinating internally, and escalating to clinical operations leadership when needed. This is an excellent opportunity for a detail-driven professional looking to grow their clinical operations career on the sponsor side Here's how you will contribute: Serve as a day-to-day operational point of contact for assigned CROs and vendors, tracking study deliverables and timelines and flagging risks or delays to clinical operations leadership. Review CRO-generated study documents for completeness and quality, including monitoring visit reports, site correspondence, protocol deviations, and TMF entries. Support the coordination of study startup activities, including site activation tracking, regulatory document collection, and vendor kick-off preparation. Maintain and update study trackers, timelines, and action logs; ensure cross-functional teams have visibility into study status and open items. Attend and support cross-functional study team meetings; document meeting minutes, track action items, and follow up on outstanding deliverables. Track and triage protocol deviations reported by CROs; coordinate with vendors and internal teams to ensure timely documentation and resolution. Support safety reporting coordination, including tracking SAE/SUSAR notifications and ensuring timely distribution to sites and relevant stakeholders in line with vendor responsibilities. Monitor TMF completeness and support inspection readiness activities, working with CROs to resolve filing gaps and maintain document quality standards. Assist with IRB/IEC tracking across study sites, including monitoring approval status for amendments and annual renewals submitted by the CRO. Compile and distribute enrollment, site performance, and operational metrics to clinical operations leadership on a regular basis. Contribute to data reviews as needed, and track data cleaning progress performed by CRO. Review and track monitoring visits and monitoring visit reports performed by CRO to ensure high quality and adherence to the monitoring plan. Support vendor invoice review and budget tracking by reconciling CRO invoices against contracted activities and flagging discrepancies. Coordinate data reconciliation activities at key study milestones in collaboration with data management and the CRO. Support the onboarding of CTAs joining the study team and serve as a resource for day-to-day study questions. The Ideal Candidate will have: Bachelor’s degree required; scientific or health-related field preferred. 6+ years of experience in clinical operations, clinical research, or a related field; sponsor-side experience is a plus. Foundational understanding of GCP, ICH guidelines, and clinical trial processes. Experience working with or alongside CROs or clinical vendors in a coordination or support capacity. Strong attention to detail and ability to manage multiple trackers, timelines, and action items simultaneously. Comfortable working in a structured, vendor-managed model where the role is one of oversight and coordination rather than direct execution. Familiarity with clinical trial systems such as CTMS, EDC, and eTMF platforms. Clear communicator with the ability to follow up consistently and escalate issues in a timely manner. Familiarity with therapeutic areas such as oncology, immunology, and/or respiratory is a plus. Ability to travel up to 20% of the time, domestically and/or internationally, as study needs require. About Generate Biomedicines We are a clinical-stage generative biology company pioneering the AI revolution in drug design and development. We are advancing a new approach to drug creation—one grounded in the ability to design proteins with defined biological intent. By integrating machine learning with large-scale experimentation, this approach aims to reduce the uncertainty, time, and cost associated with developing protein-based medicines. Founded in 2018, we are advancing a growing pipeline of clinical and preclinical programs across multiple disease areas and protein modalities. By unifying computational design and clinical development within a single operating model, we translate this approach into clinical-stage programs and are leading a shift from traditional drug discovery toward systematic drug generation. At Generate:Biomedicines, we collaborate across disciplines in new ways to invent and innovate. We bring diverse perspectives to a shared goal of delivering better medicines to patients in need, faster, guided by our values and leadership behaviors. Generate:Biomedicines is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Recruitment & Staffing Agencies: Generate:Biomedicines does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Generate:Biomedicines or its employees is strictly prohibited unless contacted directly by the Company’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Generate:Biomedicines and the Company will not owe any referral or other fees with respect thereto. LI-RT1 Compensation: The base salary range provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package. Per Year Salary Range $127,000—$170,000 USD", "summaryDescription" : "Clinical Trial Manager at Generate Biomedicines. Skills: Clinical trial management, CRO coordination, Vendor oversight. Serve as operational point of contact for CROs. Serve as operational point of contact for vendors", "postedDate" : "2026-06-12T01:38:03.003", "createdAt" : "2026-06-12T01:38:03.003", "lastUpdated" : "2026-06-14T22:50:06.003", "ingestTimestamp" : "2026-06-12T01:38:03.003", "mongoId" : "6a2ac2eb74d8ee00a06f8464", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 127000, "salaryAnnualMax" : 170000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "TMF completeness", "IRB/IEC tracking", "SAE/SUSAR notifications", "Protocol deviations", "Organized", "Clear communicator", "Attention to detail", "Clinical trial management", "CRO coordination", "Vendor oversight", "Clinical operations", "Clinical research", "Vendor management", "Study startup", "Data reviews", "Invoice review", "Budget tracking", "Data reconciliation", "Timeline management", "Action item tracking", "Clinical trial processes", "Oncology", "Immunology", "Respiratory", "CTMS platforms", "EDC platforms", "eTMF platforms" ], "skillCount" : 27, "jobCategory" : "engineering", "jobSubcategory" : "clinical-development", "dataQualityScore" : 0.8888889, "_score" : 534.7237, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a211c2874d8ee00a0b302b1", "title" : "Assistante d'essais cliniques/ Clinical Trial Assistant (CTA)", "company" : "Requires An Accommodation", "salary" : { "min" : 43900.0, "max" : 85300.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "Kirkland, Quebec, Canada", "locations" : [ "Kirkland, Quebec, Canada" ], "timestamp" : "2026-06-04T21:35:12.465", "fingerprint" : "af241caf5e240c4fe45a69642e41b2a60806f221033a3de74a5bb4f8be35049f", "source" : "workday", "language" : "fr", "applyUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Kirkland-Quebec-Canada/Assistante-d-essais-cliniques--Clinical-Trial-Assistant--CTA-_R1497777", "externalId" : "R1497777", "locationPoint" : "42.09253,-88.85121", "structuredLocations" : [ { "city" : "Kirkland", "state" : "Quebec", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "45.4529194,-73.8647559" } ], "locationText" : "Kirkland, Quebec, Canada", "employmentType" : "FULL_TIME", "minimumEducation" : "High School", "technicalSkills" : "Microsoft Word, Microsoft Excel, Microsoft PowerPoint", "professionalSkills" : [ "Clinical documentation", "Regulatory requirements", "Protocol requirements" ], "hardSkillsList" : [ "Administrative support", "Time management", "Organizational skills" ], "hardSkills" : [ { "name" : "Administrative support", "level" : "intermediate" }, { "name" : "Time management", "level" : "intermediate" }, { "name" : "Organizational skills", "level" : "intermediate" } ], "majorSkills" : "Clinical documentation, Administrative support, Regulatory compliance", "majorSkillsList" : [ "Clinical documentation", "Administrative support", "Regulatory compliance" ], "coreResponsibilities" : "Update and maintain clinical documents and systems, Track site compliance and performance, Assist with preparation, handling, distribution, filing, and archiving, Assist with periodic review of study files for, Assist with preparation, handling and distribution of Clinical, Maintain tracking information for supplies, Track and manage Case Report Forms, Manage queries, Manage clinical data flow, Act as a central contact for clinical team, Assist with designated project communications, Assist with associated documentation", "teamCollaboration" : "Clinical Research Associates; Regulatory and Start-Up teams; Clinical team", "domainKnowledge" : "Clinical research; Good Clinical Practice; ICH guidelines; Protocol requirements", "domainList" : [ "clinical-research", "good-clinical-practice", "ich-guidelines", "protocol-requirements" ], "domainSpecificKnowledge" : [ "Clinical research", "Good Clinical Practice", "ICH guidelines", "Protocol requirements" ], "toolProficiency" : [ "Trial Master File", "Microsoft Word", "Microsoft Excel", "Microsoft PowerPoint" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Clinical documentation; Filing; Archiving", "outcomesObjectives" : "Ensure complete and accurate Trial Master File delivery", "qualificationsBasic" : "High School Diploma or equivalent, 3 years administrative support experience, Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint, Written and verbal communication skills including good command of English language, Effective time management and organizational skills, Ability to establish and maintain effective working relationships with coworkers, managers, and clients", "qualificationsPreferred" : "1 year minimum experience in clinical research", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Aperçu du poste En collaboration avec les associés de recherche clinique et les équipes de réglementation et de démarrage, effectuer des tâches administratives quotidiennes afin de garantir la livraison d’un dossier principal d’essai complet et précis. Fonctions essentielles • Aider les associés de recherche clinique (ARC) et l’équipe de réglementation et de démarrage (RD) à mettre à jour et à maintenir avec précision les documents et systèmes cliniques (par exemple, le dossier principal d’essai [DPE]) qui permettent de suivre la conformité et les performances du centre dans le respect des échéances du projet. • Aider l’équipe clinique dans la préparation, la manipulation, la distribution, le classement et l’archivage de la documentation et des rapports cliniques conformément à la portée du travail et aux procédures opérationnelles normalisées. • Participer à la révision périodique des dossiers d’étude pour s’assurer qu’ils sont complets. • Aider les ARC et les RD dans la préparation, la manipulation et la distribution des fournitures d’essais cliniques et dans la maintenance des informations de suivi. • Coordonner le suivi et la gestion des cahiers d’observations, des requêtes et du flux de données cliniques. • Agir en tant que personne-ressource principale pour l’équipe clinique en ce qui concerne les communications, la correspondance et la documentation associée au projet. • Le travail peut inclure l’accompagnement des ARC lors de visites aux centres pour les aider dans leurs tâches de surveillance clinique, une fois la formation requise terminée. • Le travail peut inclure la collaboration avec l’équipe clinique sur la préparation, la manipulation, la distribution, le classement et l’archivage de la documentation et des rapports cliniques conformément à la portée du travail et aux procédures opérationnelles normalisées. Qualifications • Diplôme d’études secondaires ou équivalent requis. • 3 à 4 ans d’expérience en soutien administratif. • Combinaison équivalente d’éducation, de formation et d’expérience. • Une expérience minimale d’un an en recherche clinique est fortement souhaitée. • Compétences informatiques, y compris une connaissance pratique de Microsoft Word, d’Excel et de PowerPoint. • Compétences en matière de communication écrite et orale, y compris une bonne maîtrise de l’anglais. • Compétences organisationnelles et de gestion du temps efficaces. • Capacité à établir et à entretenir des relations de travail efficaces avec les collègues, les gestionnaires et les clients. Connaissance de base des exigences réglementaires applicables à la recherche clinique, c’est-à-dire des bonnes pratiques cliniques (BPC) et des lignes directrices du Conseil international d’harmonisation (CIH), telles qu’elles sont définies lors de la formation en entreprise. • Connaissance des exigences applicables en matière de protocole, telles qu’elles sont définies lors de la formation en entreprise. Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. • Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. • Assist with periodic review of study files for completeness. • Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. • Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training. Qualifications • High School Diploma or equivalent Req • 3 years administrative support experience. • Equivalent combination of education, training and experience. • Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint. • Written and verbal communication skills including good command of English language. • Effective time management and organizational skills. • Ability to establish and maintain effective working relationships with coworkers, managers, and clients. • Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training. • Knowledge of applicable protocol requirements as provided in company training. IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé. IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez [https://jobs.iqvia.com](https://jobs.iqvia.com/) IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable. Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au workday_recruiting@iqvia.com, afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at [https://jobs.iqvia.com](https://jobs.iqvia.com/) IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: workday_recruiting@iqvia.com, so that IQVIA can support your participation in the recruitment process. 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. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $43,900.00 - $85,300.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices. The potential base pay range for this role, when annualized, is $43,900.00 - $85,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.", "summaryDescription" : "Assistante d'essais cliniques/ Clinical Trial Assistant (CTA) at Requires An Accommodation. Skills: Clinical documentation, Administrative support, Regulatory compliance. Update and maintain clinical documents and systems. Track site compliance and performance", "postedDate" : "2026-06-02T10:33:55.791", "createdAt" : "2026-06-04T10:33:55.730", "lastUpdated" : "2026-06-04T21:35:12.465", "ingestTimestamp" : "2026-06-04T10:33:55.730", "mongoId" : "6a211c2874d8ee00a0b302b1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Kirkland-Quebec-Canada/Assistante-d-essais-cliniques--Clinical-Trial-Assistant--CTA-_R1497777", "salaryAnnualMin" : 43900, "salaryAnnualMax" : 85300, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Administrative support", "Time management", "Organizational skills", "Clinical documentation", "Regulatory compliance", "Regulatory requirements", "Protocol requirements", "Clinical research", "Good Clinical Practice", "ICH guidelines", "Trial Master File", "Microsoft Word", "Microsoft Excel", "Microsoft PowerPoint" ], "skillCount" : 14, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 527.1752, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a305b92f292fd229cf5ef8f", "title" : "Mitarbeiter ( BTA / MTLA / CTA / PTA ) – Produktion rekombinante Proteine – Downstream Processing (m|w|d)", "company" : "Miltenyi Biotec", "industry" : "Biotechnology", "salary" : { "min" : 48000.0, "max" : 65000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for Mid-level Biologics Production roles in Teterow, Germany, adjusted for industry and company size." }, "location" : "Teterow, Germany", "locations" : [ "Teterow", "Germany" ], "timestamp" : "2026-06-16T10:04:37.496", "fingerprint" : "ed461aabc3878276038bfda666a864a22e5df7ee541a200194b342e6a7b20316", "source" : "smartrecruiters", "language" : "de", "applyUrl" : "https://jobs.smartrecruiters.com/MiltenyiBiotec1/744000132170409-mitarbeiter-bta-mtla-cta-pta-produktion-rekombinante-proteine-downstream-processing-m-w-d-", "externalId" : "744000132170409", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Teterow", "country" : "Germany", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "53.7709505,12.5753569" } ], "locationText" : "Teterow, Germany", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "technicalSkills" : "Biotechnologie, Biochemie, MS-Office", "professionalSkills" : [ "Eigenverantwortliches Arbeiten", "Prozessoptimierung" ], "hardSkillsList" : [ "Proteinaufreinigung", "Ultrafiltration", "Diafiltration", "Endformulierung", "Produktionsanlagen Bedienung", "Prozessbegleitende Analytik", "Daten Auswertung" ], "hardSkills" : [ { "name" : "Proteinaufreinigung", "level" : "intermediate" }, { "name" : "Ultrafiltration", "level" : "intermediate" }, { "name" : "Diafiltration", "level" : "intermediate" }, { "name" : "Endformulierung", "level" : "intermediate" }, { "name" : "Produktionsanlagen Bedienung", "level" : "intermediate" }, { "name" : "Prozessbegleitende Analytik", "level" : "intermediate" }, { "name" : "Daten Auswertung", "level" : "intermediate" } ], "majorSkills" : "Proteinaufreinigung, Downstream Processing, GMP-konforme Aufreinigung", "majorSkillsList" : [ "Proteinaufreinigung", "Downstream Processing", "GMP-konforme Aufreinigung" ], "coreResponsibilities" : "Refolding-Prozesse durchführen, Chromatographische Aufreinigung durchführen, Ultra- und Diafiltration durchführen, Endformulierung der Proteine durchführen, Produktionsanlagen bedienen, Equipment und Chromatographiesäulen vorbereiten, Equipment und Chromatographiesäulen nachbereiten, Herstellprozesse im Reinraum durchführen, SOPs dokumentieren, Prozessbegleitende Analytik ausführen, Daten strukturiert auswerten, Herstellprozesse optimieren", "teamCollaboration" : "Engagiertes Team; Interkulturelles Umfeld", "domainKnowledge" : "Rekombinante Proteine; Therapeutische Anwendungen; Zelltherapien; Gentherapien; Krebsbehandlung; Autoimmunerkrankungen; GMP", "domainList" : [ "rekombinante-proteine", "therapeutische-anwendungen", "zelltherapien", "gentherapien", "krebsbehandlung", "autoimmunerkrankungen", "gmp" ], "domainSpecificKnowledge" : [ "Rekombinante Proteine", "Therapeutische Anwendungen", "Zelltherapien", "Gentherapien", "Krebsbehandlung", "Autoimmunerkrankungen", "GMP" ], "documentationSkills" : "SOPs dokumentieren", "continuousLearning" : "Individuelle Weiterbildung", "innovationCreativity" : "Entwicklung innovativer Therapien; Kreativität", "qualificationsBasic" : "Abgeschlossene Berufsausbildung (BTA, MTLA, CTA, PTA, Laborant), Studium (B.Sc.) in Biotechnologie, Biochemie, Gute MS-Office-Kenntnisse, Sichere Deutschkenntnisse, Sichere Englischkenntnisse", "qualificationsPreferred" : "Erfahrung in Aufreinigung bakterieller Proteine, Kenntnisse in proteinbiochemischen Methoden", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Seit 35 Jahren entwickeln wir einzigartige Lösungen für die biomedizinische Spitzenforschung sowie für neuartige Zell- und Gentherapien. Wir tragen dazu bei, medizinische Methoden zu revolutionieren, um Krebs und andere schwere Krankheiten zu besiegen. Uns kennzeichnet ein Arbeitsumfeld, das von Kreativität und eigenverantwortlichem Arbeiten geprägt ist. Bei Miltenyi Biotec arbeiten mehr als 5.000 Menschen aus über 75 Ländern zusammen und bilden die Basis für unseren nachhaltigen Erfolg. An unserem Standort in Teterow, in der Nähe von Rostock, werden Sie Teil der Abteilung „Microbial Products“. Sie arbeiten in einem engagierten Team, das sich mit der GMP-konformen Aufreinigung rekombinanter Proteine für therapeutische Anwendungen beschäftigt. Es erwartet Sie ein abwechslungsreiches Aufgabenfeld, in dem Sie aktiv an der Entwicklung und Umsetzung innovativer Therapien zur Behandlung von Krebs und Autoimmunerkrankungen mitwirken. * Sie führen Refolding-Prozesse, die chromatographische Aufreinigung sowie die Ultra- und Diafiltration bis hin zur Endformulierung der Proteine eigenständig durch. * Auch die Bedienung der Produktionsanlagen sowie die Vor- und Nachbereitung des Equipments und der Chromatographiesäulen liegen in Ihrem Verantwortungsbereich. * Die Herstellprozesse werden im Reinraum durchgeführt und gemäß den vorgegebenen SOPs dokumentiert. * Die prozessbegleitende Analytik wird von Ihnen ausgeführt und die gewonnenen Daten werden strukturiert ausgewertet. * In die kontinuierliche Optimierung der Herstellprozesse bringen Sie Ihre Erfahrung aktiv ein. ## Qualifications * Vorausgesetzt wird eine abgeschlossene Berufsausbildung bspw. im naturwissenschaftlichen, technischen Bereich (z. B. BTA, MTLA, CTA, PTA oder Laborant) oder ein Studium (B.Sc.) in Biotechnologie, Biochemie. Quereinsteiger, die Neues erlernen wollen und Freude an technischem Arbeiten mitbringen, sind gerne willkommen. * Idealerweise konnten Sie bereits Erfahrung in der Aufreinigung bakterieller Proteine sammeln und bringen Kenntnisse in proteinbiochemischen Methoden mit. * Eine sorgfältige, strukturierte und präzise Arbeitsweise zeichnet Sie aus. * Als Teamplayer sind Sie zuverlässig, hilfsbereit sowie aufgeschlossen in Ihrer Kommunikation. * Gute MS-Office-Kenntnisse sowie sichere Deutsch- und Englischkenntnisse in Wort und Schrift runden Ihr Profil ab. ## Additional Information Was wir bieten * Arbeiten mit freier und selbstbestimmter Zeiteinteilung * Ein interkulturelles Umfeld, geprägt von Vielfalt, flachen Hierarchien, Duz-Kultur * Freiräume, um sich kreativ einzubringen und aktiv mitzugestalten * Individuelle Weiterbildung in unserer Miltenyi University als Kern der Miltenyi DNA * 30-Tage-Urlaub, vergünstigtes Deutschlandticket, (E)-Bike-Leasing, vermögenswirksame Leistungen, betriebliche Altersvorsorge, Berufsunfähigkeitsversicherung, Kantine u.v.m. Vielfalt ist die Grundlage unserer Kreativität bei Miltenyi Biotec. Bringen Sie sich ein, so wie Sie sind – unabhängig von Geschlecht, sexueller Identität, Alter, Herkunft, Religion oder Behinderung. Wir freuen uns auf Ihre Bewerbung Wenn Sie in einem offenen, kreativen und hilfsbereiten Team arbeiten möchten, bieten wir Ihnen hier das richtige Umfeld. Wir freuen uns auf Ihre Bewerbung – mit Ihrer Gehaltsvorstellung und Verfügbarkeit.", "summaryDescription" : "Mitarbeiter ( BTA / MTLA / CTA / PTA ) – Produktion rekombinante Proteine – Downstream Processing (m|w|d) at Miltenyi Biotec. Skills: Proteinaufreinigung, Downstream Processing, GMP-konforme Aufreinigung. Refolding-Prozesse durchführen. 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Interkulturelles Umfeld", "domainKnowledge" : "Rekombinante Proteine; Downstream Processing; Zell- und Gentherapien; Krebsbehandlung; Autoimmunerkrankungen; Biopharmazeutische Therapien; GMP-konforme Aufreinigung", "domainList" : [ "rekombinante-proteine", "downstream-processing", "zell-und-gentherapien", "krebsbehandlung", "autoimmunerkrankungen", "biopharmazeutische-therapien", "gmp-konforme-aufreinigung" ], "domainSpecificKnowledge" : [ "Rekombinante Proteine", "Downstream Processing", "Zell- und Gentherapien", "Krebsbehandlung", "Autoimmunerkrankungen", "Biopharmazeutische Therapien", "GMP-konforme Aufreinigung" ], "documentationSkills" : "SOPs Dokumentation", "continuousLearning" : "Individuelle Weiterbildung", "innovationCreativity" : "Entwicklung innovativer Therapien; Freiräume zur Mitgestaltung", "qualificationsBasic" : "Abgeschlossene Berufsausbildung (BTA, MTLA, CTA, PTA, Laborant), Studium (B.Sc.) in Biotechnologie, Biochemie, Gute MS-Office-Kenntnisse, Sichere Deutschkenntnisse, Sichere Englischkenntnisse", "qualificationsPreferred" : "Erfahrung in Aufreinigung bakterieller Proteine, Kenntnisse in proteinbiochemischen Methoden", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Seit 35 Jahren entwickeln wir einzigartige Lösungen für die biomedizinische Spitzenforschung sowie für neuartige Zell- und Gentherapien. Wir tragen dazu bei, medizinische Methoden zu revolutionieren, um Krebs und andere schwere Krankheiten zu besiegen. Uns kennzeichnet ein Arbeitsumfeld, das von Kreativität und eigenverantwortlichem Arbeiten geprägt ist. Bei Miltenyi Biotec arbeiten mehr als 5.000 Menschen aus über 75 Ländern zusammen und bilden die Basis für unseren nachhaltigen Erfolg. An unserem Standort in Teterow, in der Nähe von Rostock, werden Sie Teil der Abteilung „Microbial Products“. Sie arbeiten in einem engagierten Team, das sich mit der GMP-konformen Aufreinigung rekombinanter Proteine für therapeutische Anwendungen beschäftigt. Es erwartet Sie ein abwechslungsreiches Aufgabenfeld, in dem Sie aktiv an der Entwicklung und Umsetzung innovativer Therapien zur Behandlung von Krebs und Autoimmunerkrankungen mitwirken. * Sie führen Refolding-Prozesse, die chromatographische Aufreinigung sowie die Ultra- und Diafiltration bis hin zur Endformulierung der Proteine eigenständig durch. * Auch die Bedienung der Produktionsanlagen sowie die Vor- und Nachbereitung des Equipments und der Chromatographiesäulen liegen in Ihrem Verantwortungsbereich. * Die Herstellprozesse werden im Reinraum durchgeführt und gemäß den vorgegebenen SOPs dokumentiert. * Die prozessbegleitende Analytik wird von Ihnen ausgeführt und die gewonnenen Daten werden strukturiert ausgewertet. * In die kontinuierliche Optimierung der Herstellprozesse bringen Sie Ihre Erfahrung aktiv ein. ## Qualifications * Vorausgesetzt wird eine abgeschlossene Berufsausbildung bspw. im naturwissenschaftlichen, technischen Bereich (z. B. BTA, MTLA, CTA, PTA oder Laborant) oder ein Studium (B.Sc.) in Biotechnologie, Biochemie. Quereinsteiger, die Neues erlernen wollen und Freude an technischem Arbeiten mitbringen, sind gerne willkommen. * Idealerweise konnten Sie bereits Erfahrung in der Aufreinigung bakterieller Proteine sammeln und bringen Kenntnisse in proteinbiochemischen Methoden mit. * Eine sorgfältige, strukturierte und präzise Arbeitsweise zeichnet Sie aus. * Als Teamplayer sind Sie zuverlässig, hilfsbereit sowie aufgeschlossen in Ihrer Kommunikation. * Gute MS-Office-Kenntnisse sowie sichere Deutsch- und Englischkenntnisse in Wort und Schrift runden Ihr Profil ab. ## Additional Information Was wir bieten * Arbeiten mit freier und selbstbestimmter Zeiteinteilung * Ein interkulturelles Umfeld, geprägt von Vielfalt, flachen Hierarchien, Duz-Kultur * Freiräume, um sich kreativ einzubringen und aktiv mitzugestalten * Individuelle Weiterbildung in unserer Miltenyi University als Kern der Miltenyi DNA * 30-Tage-Urlaub, vergünstigtes Deutschlandticket, (E)-Bike-Leasing, vermögenswirksame Leistungen, betriebliche Altersvorsorge, Berufsunfähigkeitsversicherung, Kantine u.v.m. Vielfalt ist die Grundlage unserer Kreativität bei Miltenyi Biotec. Bringen Sie sich ein, so wie Sie sind – unabhängig von Geschlecht, sexueller Identität, Alter, Herkunft, Religion oder Behinderung. Wir freuen uns auf Ihre Bewerbung Wenn Sie in einem offenen, kreativen und hilfsbereiten Team arbeiten möchten, bieten wir Ihnen hier das richtige Umfeld. Wir freuen uns auf Ihre Bewerbung – mit Ihrer Gehaltsvorstellung und Verfügbarkeit.", "summaryDescription" : "Mitarbeiter ( BTA / MTLA / CTA / PTA ) – Produktion rekombinante Proteine – Downstream Processing (m|w|d) at Miltenyi Biotec. Skills: Proteinaufreinigung, GMP-konforme Produktion, Biopharmazeutische Produktion. Durchführung von Refolding-Prozessen. 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Tel Aviv, Israel; United States", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Clinical trial management", "Regulatory compliance", "Vendor management", "Budget development", "Protocol development", "Risk mitigation", "Data collection", "Inspection readiness", "Audit preparation" ], "hardSkillsList" : [ "Clinical operations", "Global clinical trials", "Immunology indications", "Autoimmune diseases", "Inflammatory diseases", "Monoclonal antibodies", "Advanced therapies", "Clinical trial regulations", "Operational best practices", "Pivotal trials" ], "softSkillsList" : [ "Leadership", "Problem-solving" ], "hardSkills" : [ { "name" : "Clinical operations", "level" : "intermediate" }, { "name" : "Global clinical trials", "level" : "intermediate" }, { "name" : "Immunology indications", "level" : "intermediate" }, { "name" : "Autoimmune diseases", "level" : "intermediate" }, { "name" : "Inflammatory diseases", "level" : "intermediate" }, { "name" : "Monoclonal antibodies", "level" : "intermediate" }, { "name" : "Advanced therapies", "level" : "intermediate" }, { "name" : "Clinical trial regulations", "level" : "intermediate" }, { "name" : "Operational best practices", "level" : "intermediate" }, { "name" : "Pivotal trials", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Problem-solving" } ], "majorSkills" : "Clinical trial operations, Global study execution, Immunology trials", "majorSkillsList" : [ "Clinical trial operations", "Global study execution", "Immunology trials" ], "coreResponsibilities" : "Lead operational strategy, Plan clinical trials, Execute clinical trials, Oversee clinical trials, Serve as primary operational point of contact, Oversee selection of CROs, Oversee management of vendors, Drive site feasibility, Drive site selection, Drive site activation, Drive patient recruitment strategies, Manage ongoing site management, Develop study timelines, Maintain study timelines, Develop risk mitigation strategies, Maintain risk mitigation strategies, Develop operational tracking tools, Maintain operational tracking tools, Collaborate on protocol development, Collaborate on CRF design, Collaborate on ICF review, Collaborate on operational study plans, Ensure studies are conducted in compliance, Identify operational issues, Resolve operational issues, Escalate risks, Implement mitigation strategies, Oversee data collection activities, Oversee database lock readiness, Support data review processes, Contribute to regulatory filings, Contribute to inspection readiness, Contribute to audit preparation, Provide leadership to Clinical Operations team, Provide mentorship to Clinical Operations team, Contribute to process improvement initiatives", "teamCollaboration" : "Internal cross-functional teams; External partners; CROs and vendors; Clinical Operations team members", "projectManagementSkills" : [ "Study timelines", "Risk mitigation", "Operational tracking" ], "domainKnowledge" : "Immunology; Autoimmune diseases; Inflammatory diseases; Biologics; Monoclonal antibodies; Advanced therapies; GCP/ICH guidelines; Clinical trial regulations", "domainList" : [ "immunology", "autoimmune-diseases", "inflammatory-diseases", "biologics", "monoclonal-antibodies", "advanced-therapies", "gcp-ich-guidelines", "clinical-trial-regulations" ], "domainSpecificKnowledge" : [ "Immunology", "Autoimmune diseases", "Inflammatory diseases", "Biologics", "Monoclonal antibodies", "Advanced therapies", "GCP/ICH guidelines", "Clinical trial regulations" ], "toolProficiency" : [ "CTMS", "EDC", "eTMF", "Risk-based monitoring tools" ], "documentationSkills" : "CRF design; ICF review; Operational study plans; Regulatory filings", "problemSolvingSkills" : "Problem-solving; Risk mitigation; Issue resolution", "specialRequirements" : "Periodic travel to Beeline Medicines offices, Domestic and international travel up to 20%", "outcomesObjectives" : "Ensure studies delivered on time; Ensure studies within scope; Ensure compliance with regulatory standards; Achieve enrollment goals", "qualificationsBasic" : "Bachelor’s degree in life sciences, Minimum 5 years of experience in clinical operations, At least 3 years in a Senior CTM role, Proven track record of managing global clinical trials, Experience with biologics, Knowledge of GCP/ICH guidelines, Availability during Eastern Time (ET) business hours", "qualificationsPreferred" : "Advanced degree preferred, Experience in rare autoimmune indications, Familiarity with adaptive trial designs, Experience in early- to late-stage development programs", "workSiteFlexibility" : "Hybrid", "rawDescription" : "About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully. Job Summary: The Senior Clinical Trial Manager (Sr. CTM) will lead the operational planning, execution, and oversight of complex, global clinical studies in the field of immunology and autoimmune diseases. This role is responsible for ensuring studies are delivered on time, within scope, and in compliance with regulatory standards, Good Clinical Practice (GCP), and company Standard Operating Procedures (SOPs). The Sr. CTM will partner closely with internal cross-functional teams (Clinical Development, Regulatory, Biometrics, Safety, and Quality) and external partners (CROs, vendors, and sites) to ensure operational excellence. This individual will also play a critical role in driving strategic decision-making and supporting inspection readiness and regulatory submissions. Work Arrangement the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company's discretion based on business need. Essential Duties and Responsibilities: Lead the operational strategy, planning, and execution of global Phase 1–4 clinical trials in immunology indications (e.g., autoimmune and inflammatory diseases). Serve as the primary operational point of contact for internal stakeholders and external partners. Oversee the selection and management of CROs and other vendors, including scope of work, budget development, contracting, and performance oversight. Drive site feasibility, site selection, activation, patient recruitment strategies, and ongoing site management to ensure achievement of enrollment goals. Develop and maintain study timelines, risk mitigation strategies, and operational tracking tools. Collaborate with cross-functional teams on protocol development, CRF design, ICF review, and development of operational study plans. Ensure studies are conducted in compliance with GCP/ICH guidelines, local regulatory requirements, and internal SOPs. Proactively identify and resolve operational issues, escalating risks and implementing mitigation strategies as needed. Oversee data collection activities, database lock readiness, and support data review processes. Contribute to regulatory filings, inspection readiness, and audit preparation. Provide leadership and mentorship to Clinical Operations team members. Contribute to process improvement initiatives within Clinical Operations to enhance efficiency and quality. Perform other duties and responsibilities as assigned Qualifications: Education: Bachelor’s degree in life sciences or related field (advanced degree preferred) Minimum 5 years of experience in clinical operations in the biopharmaceutical industry, with at least 3 years in a Senior CTM or equivalent leadership role. Proven track record of managing global, multi-center clinical trials in immunology or autoimmune disease indications. Experience with biologics, monoclonal antibodies, or advanced therapies. Strong knowledge of GCP/ICH guidelines, clinical trial regulations, and operational best practices. Experience in rare autoimmune indications or immune-mediated inflammatory diseases. Familiarity with adaptive trial designs or complex biomarker-driven studies. Experience in early- to late-stage development programs, including pivotal trials. Proficiency with electronic systems such as CTMS, EDC, eTMF, and risk-based monitoring tools. Ability to thrive in a fast-paced, dynamic environment and work independently with minimal supervision Excellent communication, leadership, and problem-solving skills. This position requires availability during Eastern Time (ET) business hours This role may require domestic and international travel, including overnight stays, up to 20% or more based on business needs Salary Range: The expected annual salary range for this position is listed below. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance. Salary Range $178,000—$194,500 USD Benefits: We offer a comprehensive benefits package including: Medical, Dental & Vision insurance (employee premiums 100% covered by company) 20 accrued days combined time off (PTO/Sick), 12 company holidays, & winter recharge Flexible work arrangements / hybrid schedule Health Savings Account (HSA) *Benefits are subject to eligibility requirements and plan terms. Additional details provided during the offer process* Equal Employment Opportunity: Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. Reasonable Accommodation: If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates. Privacy Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at Privacy Policy - Beeline Medicines", "summaryDescription" : "Senior Clinical Trial Manager (Lupus) at Beeline Medicines. Skills: Clinical trial operations, Global study execution, Immunology trials. Lead operational strategy. 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Collaborate with GM Quebec", "domainKnowledge" : "Veterinary medicine; Healthcare sector", "domainList" : [ "veterinary-medicine", "healthcare-sector" ], "domainSpecificKnowledge" : [ "Veterinary medicine", "Healthcare sector" ], "communicationSkills" : "Communication skills", "problemSolvingSkills" : "Problem solving", "outcomesObjectives" : "Maximize client access; Maximize team well-being", "qualificationsBasic" : "3-5 years operations experience, 3-5 years clinic management experience, 3-5 years team management experience, Fluency in French, Working proficiency in English", "qualificationsPreferred" : "Experience in veterinary medicine, Experience in healthcare sector", "workSiteFlexibility" : "Onsite", "rawDescription" : "(English follows) À Propos de Royal Vet: Royal Vet est un nouveau concept de clinique vétérinaire, qui a pour mission de réinventer l'expérience des soins aux animaux de compagnie. Nous sommes fondés et dirigés par des vétérinaires, plaçant le bien-être de notre personnel au premier plan de nos activité s. Ce faisant, notre équipe est en mesure de fournir, avec compassion, des soins primaires et d'urgence aux animaux de compagnie en besoin. Le Rôle: Nous sommes à la recherche d'un(e) Gestionnaire de Clinique exceptionnel(le) pour diriger notre clinique Rosemont à Montréal, à deux pas du marché Jean-Talon! Relevant directement du Directeur Général, Québec, le ou la Gestionnaire de Clinique sera responsable des opérations quotidiennes et de la performance de la clinique. Vous dirigerez une équipe multidisciplinaire de technicien(ne)s et de personnel de soutien, tout en travaillant en étroite collaboration avec l'équipe de direction pour façonner la culture, l'expérience client et la réussite de la clinique. Vous correspondez au candidat idéal si vous êtes un(e) opérateur(rice) terrain doté(e) d'un fort leadership, d'excellentes compétences en communication, d'un bon sens des indicateurs de performance et d'une réelle passion pour le développement d'équipes performantes dans un environnement vibrant. Responsabilités: Opérations et performance de la clinique Diriger les opérations quotidiennes de la clinique Rosemont en assurant des soins exceptionnels aux patients exceptionnel et une performance opérationnelle solide Suivi et optimisation des indicateurs clés de la clinique — de la satisfaction des clients à la capacité d'accueil — grâce à des réunions de suivi régulières et à des séances de planification en collaboration avec le directeur général du Québec Gérer le calendrier de la clinique, la prise de rendez-vous et la planification des capacités afin de maximiser à la fois l'accès des clients et le bien-être de l'équipe Administrer le logiciel de gestion (Practice Management Software), le mettre à jour et l'adapter aux besoins évolutifs de l'équipe Gérer les niveaux de stock, les relations avec les fournisseurs et les ressources nécessaires au fonctionnement optimal de la clinique Assurer la conformité avec les normes de sécurité, réglementaires et professionnelles applicables au Québec Leadership d'équipe Recruter, intégrer, coacher et développer l'équipe de support de la clinique Approuver et contrôler les feuilles de temps, les horaires et les demandes de congés Identifier les opportunités de développement pour les membres de l'équipe, fournir un feedback régulier et assurer une croissance continue Défendre les intérêts de votre équipe afin qu'elle se sente écoutée et que son point de vue soit pris en compte lors des discussions avec l'équipe de direction Maintenir une culture qui met l'accent sur l'équilibre entre vies professionnelle et privée, la flexibilité, la compassion et un environnement exempt de reproches et de jugements Expérience client et croissance Assurer un excellent service à la clientèle et veiller à ce que les situations délicates soient traitées personnellement et rapidement Identifier des occasions d'améliorer le parcours client, de la prise de rendez-vous au suivi post-visite Collaborer avec le Directeur Général, Québec à l'exécution d'initiatives de croissance locale, d'engagement communautaire et d'amélioration opérationnelle Résoudre les problèmes, lever les obstacles et soutenir les besoins de l'équipe au quotidien Expérience et Compétences: 3 à 5 ans d'expérience en opérations, gestion de clinique ou gestion d'équipe Un(e) leader confirmé(e) : vous savez inspirer, développer et responsabiliser une équipe Solides aptitudes analytiques; à l'aise avec le suivi de KPIs opérationnels et l'utilisation des données pour décider Un état d'esprit de bâtisseur(se) : pragmatique, débrouillard(e), prêt(e) à mettre la main à la pâte Grande intelligence émotionnelle et compétences exceptionnelles en communication Maîtrise du français et bonne connaissance pratique de l'anglais (Rosemont dessert une clientèle principalement francophone) Une expérience en médecine vétérinaire ou dans le secteur de la santé est un atout, mais n'est pas requise Pourquoi se joindre à nous? Faites partie de la solution: Jouez un rôle clé dans la prestation de soins vétérinaires exceptionnels, tout en contribuant à façonner l'avenir du secteur, tant pour les vétérinaires que pour les animaux de compagnie. Une culture unique et \"fun!\": Faites partie d'une culture qui s'articule autour de l'équilibre, du soutien et de l'évolution de carrière de chaque membre de l'équipe. Un environnement de travail moderne: Travailler dans une clinique moderne, soutenue par la technologie, qui trouve un équilibre entre une belle esthétique et un flux de travail réfléchi Avantages compétitifs, dont: Des assurances santé, dentaire, vision Vacances et jours de congé payés Rabais en clinique et dans la communauté Aide au transport (e.g., remboursement de carte OPUS) Venez comme vous êtes. Fier d'être un employeur pour l'égalité des chances, Royal Vet s'engage à créer un lieu de travail diversifié et inclusif pour tous. Les candidats qualifiés seront pris en compte indépendamment de leur citoyenneté, de leur origine ethnique, de leur race, de leur couleur, de leur religion, de leur sexe, de leur identité ou expression sexuelle, de leur orientation sexuelle, de leur handicap, de leur âge ou de leur statut d'ancien combattant. --- About Royal Vet Royal Vet is a new breed of veterinary clinic on a mission to reinvent the pet care experience. We are veterinarian-founded and veterinarian-led, putting the wellbeing of our staff at the forefront of what we do. In doing so, our team can consistently deliver compassionate primary and urgent care to pets in need. The Role: We are looking for an outstanding Practice Manager to lead our Rosemont clinic in Montreal, just steps away from the Jean Talon market! Reporting directly to the General Manager, Quebec, the Practice Manager will own the day-to-day operations and performance of the clinic. You will lead a multidisciplinary team of technicians and support staff, while partnering with senior leadership to shape the culture, client experience, and overall success of the practice. You are the ideal candidate if you are a hands-on operator with strong leadership instincts, exceptional communication skills, a sharp eye for operational KPIs, and a genuine passion for building high-performing teams in a fast-paced environment. Key responsibilities: Clinic operations and performance Leading day-to-day operations at the Rosemont clinic, ensuring outstanding patient care and strong operational performance Tracking and driving key clinic metrics — from client satisfaction to capacity — with regular check-ins and planning sessions alongside the Quebec General Manager Managing the clinic calendar, appointment scheduling, and capacity planning to maximize both client access and team well-being Administering the Practice Management Software, updating and adapting it to the evolving needs of the team Managing inventory levels, supplier relationships, and the resources needed for optimal clinic operations Ensuring compliance with safety, regulatory, and professional standards applicable in Quebec Team leadership Hiring, onboarding, coaching, and developing the clinic's support team Approving and monitoring staff timesheets, schedules, and time-off requests Identifying development opportunities for team members, providing regular feedback and accountability to ensure ongoing growth Advocating for your team to ensure they feel heard and their perspective is visible during leadership discussions Implementing a culture that emphasizes work/life balance, flexibility, compassion, and a blame- and judgment-free environment Client experience and growth Delivering excellent client service, and ensuring escalations are addressed personally and promptly Identifying opportunities to improve the client journey, from booking through follow-up Partnering with the GM, Quebec to execute local growth initiatives, community engagement, and operational improvements Solving problems, removing roadblocks, and supporting the team's needs as they arise Your Qualifications 3–5 years of experience in operations, clinic management, or team-management roles A proven people leader: you know how to inspire, develop, and hold a team accountable Strong analytical skills; comfortable tracking operational KPIs and using data to make decisions A builder's mindset: hands-on, resourceful, and ready to roll up your sleeves Operates with high emotional intelligence and exceptional communication skills Fluency in French and working proficiency in English (Rosemont serves a primarily French-speaking clientele) Experience in veterinary medicine or healthcare is a plus, but not required What’s in it for you? Be part of the solution: Play a key role in delivering exceptional veterinary care, while also playing part in reshaping the future of the industry for both vets and pets. A fun and distinctive culture: Be part of a culture intently built around offering balance, support and career growth to every team member A new era work environment: Work in a modern, tech-supported clinic that strikes a balance between beautiful aesthetics and thoughtful workflow. Competitive salary and benefits, such as: Health, dental, vision insurance Paid vacation, stat days and sick days In-clinic and community discounts Commuter benefits (e.g., Opus card coverage) Come as you are. As a proud equal-opportunity employer, Royal Vet is dedicated to creating a diverse and inclusive workplace for everyone. 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"Clinical Trial Manager", "company" : "Care Access", "industry" : "Healthcare", "salary" : { "min" : 95000.0, "max" : 145000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for Clinical Trial Manager in Canada, adjusted for manager seniority and remote work mode." }, "location" : "Canada", "locations" : [ "Canada" ], "timestamp" : "2026-06-14T09:25:43.780", "fingerprint" : "23cdf70f94f3032d4229ed46fba4c2c53b0cbce25092c2c664ca0d6f333403b4", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/careaccess/jobs/4280445009", "externalId" : "4280445009", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Canada", "continent" : "na", "workMode" : "remote" } ], "locationText" : "Canada", "experienceLevel" : "Manager", "professionalSkills" : [ "Protocol execution", "Quality planning", "Risk management", "Data-driven decisions", "Project implementation", "Study startup", "Site 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coordination", "level" : "intermediate" }, { "name" : "Vendor coordination", "level" : "intermediate" }, { "name" : "Project performance monitoring", "level" : "intermediate" }, { "name" : "Contingency plan development", "level" : "intermediate" }, { "name" : "Task prioritization", "level" : "intermediate" }, { "name" : "Priority setting", "level" : "intermediate" }, { "name" : "Training needs assessment", "level" : "intermediate" }, { "name" : "Training needs coordination", "level" : "intermediate" }, { "name" : "Escalation process management", "level" : "intermediate" }, { "name" : "Quality review findings", "level" : "intermediate" }, { "name" : "Peer feedback analysis", "level" : "intermediate" }, { "name" : "Best practice collaboration", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Clinical trial management, Operational planning, Stakeholder management", "majorSkillsList" : [ "Clinical trial management", "Operational planning", "Stakeholder management" ], "coreResponsibilities" : "Drive successful execution of protocols, Drive successful execution of projects, Support building strategy to deliver trial, Support building strategy to deliver project, Monitor project status, Analyze project status, Ensure successful completion of project parameters, Ensure successful completion of project milestones, Ensure successful completion of project timetables, Proactively manage risks on trials, Proactively manage risks on projects, Implement mitigations, Act as principal liaison between Sponsor, Act as principal liaison between Care Access, Facilitate information flow, Escalate issues, Escalate potential issues, Provide timely project updates, Coordinate cross functional team, Support delivery of clinical trial, Hold teams accountable for delivery, Hold teams accountable for success, Lead teams to successfully deliver, Coordinate activities of functional departments, Coordinate activities of vendors, Develop plans for project implementation, Develop guidelines for project implementation, Identify required data, Identify required analytics, Allow data-driven decisions, Continuously monitor project performance, Evaluate growth opportunities, Develop strategy for initiatives, Identify potential risks, Develop contingency plans, Plan study specific tasks, Communicate study specific tasks, Plan project priorities, Communicate project priorities, Ensure appropriate assessment of training needs, Ensure appropriate coordination of training needs, Maintain project logs, Maintain project trackers, Support essential documentation, Support follow up of monitoring visits, Provide recommendations to challenges, Provide alternative resolutions to challenges, Ensure guidelines are followed, Ensure processes are followed, Escalate out of parameter issues, Escalate identified findings from reviews, Collaborate on best practices, Lead study startup process, Support site evaluation visits, Support site selection visits, Have sites selected, Have sites successfully activated, Review study information, Liaise with key stakeholders, Communicate study needs, Communicate site needs, Communicate performance expectations, Establish timelines, Help address questions onsite, Assess risks onsite, Mitigate issues onsite, Initiate study related processes, Partner with client to drive startup, Drive startup activities, Drive startup timelines, Drive expectations of startup process, Ensure information transition to sites, Assess study start up processes, Optimize study start up processes, Enhance efficiency, Enhance productivity, Monitor key performance indicators, Track progress, Identify areas of improvement, Be main point of contact with sponsor, Drive study activation", "teamCollaboration" : "Cross functional team; Global organization stakeholders; Fellow CTMs; Department leadership; Client communication", "projectManagementSkills" : [ "Project execution", "Timeline management", "Budget management", "Quality standards", "Risk management", "Mitigation implementation", "Project updates", "Project planning", "Project implementation", "Project performance", "Contingency planning", "Task prioritization", "Priority setting", "Study startup", "Startup activities", "Startup timelines" ], "domainKnowledge" : "Clinical trial protocols; Regulatory requirements; Decentralized trial model; Therapeutic areas", "domainList" : [ "clinical-trial-protocols", "regulatory-requirements", "decentralized-trial-model", "therapeutic-areas" ], "domainSpecificKnowledge" : [ "Clinical trial protocols", "Regulatory requirements", "Decentralized trial model", "Therapeutic areas" ], "toolProficiency" : [ "Care Access tools" ], "communicationSkills" : "Information flow; Project updates; Interpersonal communication; Written communication; Verbal communication", "documentationSkills" : "Essential documentation; Project logs; Project trackers", "problemSolvingSkills" : "Problem-solving; Risk management; Mitigation; Issue escalation; Alternative resolutions; Challenge resolution", "specialRequirements" : "Less than 25% travel, Occasional planned travel, Use keyboards, Use computer equipment", "outcomesObjectives" : "Successful execution of protocols; Successful execution of projects; Successful completion of project parameters; Successful completion of project milestones; Successful completion of project timetables; Successful delivery in areas; Successful site activation", "qualificationsBasic" : "Exceptional strategic thinking, Problem-solving skills, Effective leadership skills, Communication competency, Ability to foster team productivity, Ability to foster team cohesiveness, Ability to show flexibility, Ability to pivot workflows, Ability to adjust priorities, Ability to work independently, Organize work with attention to detail, Demonstrated skill in assessing timelines, Coordinating numerous assignments, Coordinating numerous projects simultaneously, High degree of discretion, Ability to work flexible hours, Ability to mentor junior team members, Excellent written communication skills, Excellent verbal communication skills, Excellent interpersonal communication skills, Comfortable in a fast-paced environment, Experience anticipating problems, Experience resolving problems on projects, Experience reporting project details", "qualificationsPreferred" : "Experience with decentralized trial model", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About Care Access Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow. With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all. To learn more about Care Access, visit www.CareAccess.com. How This Role Makes a Difference The Clinical Trial Manager is a central leadership role within all (study) operations. The CTM is responsible to drive the successful execution of protocols or projects, including within the decentralized trial model when applicable, from strategic planning through close out within agreed upon timelines, budget, alignment with all applicable SOPs and regulatory requirements. The CTM would serve as a key operational component at the site and play a role in staff performance, protocol compliance, and long-term quality planning. How You'll Make An Impact Drives and Manages studies or projects according to scope of work, timelines, and quality standards. Supports building a strategy to deliver the trial or project as per protocol and timelines. Monitors and analyses project status to ensure successful completion of project parameters, milestones, timetables. Understands proactively manages risks on trials or projects and implements mitigations whilst working in a cross functional team. Acts as principal liaison between Sponsor and Care Access by facilitating the flow of information between Care Access and client. Appropriately escalates any issues or potential issues as per escalation pathways; and provides timely project updates to upline management and/or Senior Leadership at Care Access. Coordinates a cross functional team to support delivery of the clinical trial. Holds teams accountable for delivery and success of the trial. Leads teams to successfully deliver in their areas. Coordinates activities of all functional departments and vendors involved in the project. Works with team and management to develop plans/guidelines for project implementation using Care Access tools.  Identifies data and analytics required to allows data-driven decisions and continuously monitors ongoing project performance. Evaluates growth opportunities of current engagement or potential engagements; helps develops the strategy for various initiatives. Works with team to identify potential risks, develop contingency plans. Plans and communicates to team members to study specific tasks and priorities for projects.  Ensures that appropriate assessment and coordination of project/protocol specific and therapeutic area training needs and activities are occurring for the team members as needed. Maintains project logs and trackers. Supports essential documentation and follow up of monitoring visits Provides recommendations and alternative resolutions to project-specific challenges through established escalation channels. Ensures guidelines and processes are followed for efficient escalation of out of parameter issues as appropriate. Escalates identified findings from periodic quality reviews and peer feedback reports. Collaborates with fellow CTMs and department leadership on best practices. Study Start Up: Lead the process of study startup to support site evaluation/selection visits on each new study and help to have sites selected and successfully activated, based off of study requirements Review study information and liaise with key stakeholders across the global organization to communicate study/site needs, requirements, performance expectations and establish timelines Work closely with the staff onsite to help address questions, assess risks and mitigate issues throughout startup Partner with other Care Access teams to initiate study related processes at the appropriate SSU milestone (e. g. capacity planning, systems build requests, etc.) Partner and communicate with client to drive startup activities, timelines, and expectations of Care Access startup process Ensure that all information gained during the startup process is completely transitioned to sites, as required Continue to assess and optimize study start up processes to enhance efficiency and productivity Monitor key performance indicators to track progress and identify areas of improvement Be main point of contact with the sponsor to drive study activation The Expertise Required Exceptional strategic thinking and problem-solving skills to drive Care Access goals while fostering and maintaining a strong client relationship. Effective leadership skills, strong communication competency, and proven ability to foster team productivity and cohesiveness. Ability to show flexibility by pivoting workflows and adjusting priorities as needed. Ability to work independently, organize work with attention to detail ‎and accuracy; demonstrated skill in assessing timelines and coordinating numerous ‎assignments and projects simultaneously under heavy and fluctuating workloads and ‎conflicting deadlines. High degree of discretion in dealing with confidential information. Ability and willingness to work flexible hours when needed. Ability to mentor junior team members. Excellent written, verbal, and interpersonal communication skills. Comfortable in a fast-paced environment. Certifications/Licenses, Education, and Experience Must have clinical trial experience. Decentralized clinical trial experience, preferred. Site experience, preferably in a site network. PMP Certification, preferred. Bachelor's degree Must have 6+ years of experience in the clinical trial/pharmaceutical industry. Must have 4+ years in project management including client management. Must have 1-2 years strategy consulting experience. Experience with oversight of external vendors (e.g., e-consent vendor). Experience collaborating and leading cross-functional teams in a matrix environment. Experience managing multiple projects across various therapeutic areas. Experience anticipating and resolving problems on projects. Experience reporting project details to various stakeholders within the company and outside of the company How We Work Together Location: Remote within Canada. This role requires 100% of work to be performed in a remote office environment. Travel: This is a remote position with less than 25% national travel requirements. Occasional planned travel may be required as part of the role. Physical demands associated with this position Include: The ability to use keyboards and other computer equipment. Benefits & Perks Paid Time Off (PTO) and Company Paid Holidays Medical, dental, and vision insurance plan options Diversity & Inclusion We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Care Access is unable to sponsor work visas at this time. If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com Mandatory Employer Disclosures: Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment. Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment. Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws. Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.", "summaryDescription" : "Clinical Trial Manager at Care Access. Skills: Clinical trial management, Operational planning, Stakeholder management. Drive successful execution of protocols. Drive successful execution of projects", "postedDate" : "2026-06-11T19:09:32.785", "createdAt" : "2026-06-11T19:09:32.785", "lastUpdated" : "2026-06-14T09:25:43.780", "ingestTimestamp" : "2026-06-11T19:09:32.785", "mongoId" : "6a2a5cee74d8ee00a06172dc", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Regulatory requirements", "Staff performance", "Protocol compliance", "Project status monitoring", "Project status analysis", "Functional departments coordination", "Vendor coordination", "Project performance monitoring", "Contingency plan development", "Task prioritization", "Priority setting", "Training needs assessment", "Training needs coordination", "Escalation process management", "Quality review findings", "Peer feedback analysis", "Best practice collaboration", "Leadership", "Mentoring", "Clinical trial management", "Operational planning", "Stakeholder management", "Protocol execution", "Quality planning", "Risk management", "Data-driven decisions", "Project implementation", "Study startup", "Site evaluation", "Site selection", "Capacity planning", "Systems build", "Project execution", "Timeline management", "Budget management", "Quality standards", "Mitigation implementation", "Project updates", "Project planning", "Project performance", "Contingency planning", "Startup activities", "Startup timelines", "Clinical trial protocols", "Decentralized trial model", "Therapeutic areas", "Care Access tools" ], "skillCount" : 47, "jobCategory" : "other", "jobSubcategory" : "trial-management", "dataQualityScore" : 0.8888889, "_score" : 514.52435, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a2c6a8f74d8ee00a090c9c7", "title" : "Manager/Sr. Manager, Clinical Operations", "company" : "LifeMine Therapeutics", "industry" : "Biotech", "salary" : { "min" : 155000.0, "max" : 215000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Biotech industry in the United States, adjusted for Manager seniority in the Boston-Cambridge metro area." }, "location" : "Watertown, Massachusetts, United States", "locations" : [ "Watertown", "Massachusetts", "United States" ], "timestamp" : "2026-06-16T01:29:08.969", "fingerprint" : "097231c3c7e25bdd268e5eaee66838b2aac553ce796366030c3cda82d76ccb55", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/lifeminetx/jobs/8587930002", "externalId" : "8587930002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Watertown", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3652576,-71.1843234" } ], "locationText" : "Watertown, Massachusetts, United States", "minimumEducation" : "Bachelor's", "experienceMinYears" : 3, "experienceLevel" : "Manager", "professionalSkills" : [ "Contract negotiation", "Performance oversight" ], "hardSkillsList" : [ "Clinical trial design", "Clinical trial execution", "Regulatory requirements" ], "softSkillsList" : [ "Leadership", "Problem-solving" ], "hardSkills" : [ { "name" : "Clinical trial design", "level" : "intermediate" }, { "name" : "Clinical trial execution", "level" : "intermediate" }, { "name" : "Regulatory requirements", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Problem-solving" } ], "majorSkills" : "Clinical operations management, Clinical trial execution, Vendor management", "majorSkillsList" : [ "Clinical operations management", "Clinical trial execution", "Vendor management" ], "coreResponsibilities" : "Manage clinical trials execution, Provide strategic oversight, Oversee operational aspects, Develop protocols, Select sites, Negotiate contracts, Manage vendors, Manage monitoring activities, Manage data collection, Set-up clinical trial trackers, Update clinical trial trackers, Work with cross-functional teams, Ensure documentation submission, Develop clinical trial processes, Implement risk management strategies, Implement monitoring plans, Implement quality assurance initiatives, Track clinical trial progress, Report on clinical trial progress, Address trial issues, Address trial risks, Act as liaison, Ensure effective communication, Ensure timely decision-making, Stay up-to-date with industry trends, Stay up-to-date with regulatory changes, Stay up-to-date with best practices, Drive continuous improvement", "teamCollaboration" : "Cross-functional teams; External vendors; Clinical trial sites", "projectManagementSkills" : [ "Clinical trial management" ], "domainKnowledge" : "Good Clinical Practices; GCP; FDA; EMA; ICH-GCP; Clinical development lifecycle", "domainList" : [ "good-clinical-practices", "gcp", "fda", "ema", "ich-gcp", "clinical-development-lifecycle" ], "domainSpecificKnowledge" : [ "Good Clinical Practices", "GCP", "FDA", "EMA", "ICH-GCP", "Clinical development lifecycle" ], "documentationSkills" : "Clinical trial documentation", "continuousLearning" : "Stay up-to-date with industry trends; Stay up-to-date with regulatory changes; Stay up-to-date with clinical trial best practices", "problemSolvingSkills" : "Problem-solving skills", "specialRequirements" : "Ability to travel as needed", "outcomesObjectives" : "Ensuring successful delivery on time; Ensuring successful delivery within budget", "qualificationsBasic" : "Bachelor's or Master's degree, 3 years of experience in clinical operations, 5 years of experience in clinical operations, Knowledge of clinical trial design, Knowledge of clinical trial execution, Knowledge of regulatory requirements, Managing multi-site clinical trials, Experience working with CROs, Experience working with vendors, Experience working with clinical trial sites, Contract negotiation, Performance oversight, Proficiency in clinical trial management systems", "qualificationsPreferred" : "Master's degree in Life Sciences", "rawDescription" : "What’s the opportunity? LifeMine Therapeutics is seeking an experienced and results-driven Manager/Sr Manager, Clinical Operations to join our growing Clinical Development team. Reporting to the Director of Clinical Operations, this individual will play a key role in the planning, execution, and management of clinical trials, ensuring successful delivery on time and within budget, while adhering to regulatory requirements and company objectives. The Manager/Sr Manager will work cross-functionally with R&D and external vendors, providing leadership and oversight throughout the clinical development lifecycle. Key Responsibilities: Manage the execution of clinical trials, ensuring that trials are conducted according to the highest standards, in compliance with Good Clinical Practices (GCP), and within timelines and budget. Provide strategic oversight and direction for clinical operations, ensuring alignment with corporate objectives and regulatory requirements. Oversee the operational aspects of clinical studies, including protocol development, site selection, contract negotiations, vendor management, monitoring activities, and data collection. Set-up and update clinical trial-related trackers such as startup progress, screening/enrollment, study invoices/payments, etc. Work closely with cross-functional teams to ensure smooth integration of all clinical operations activities. Ensure timely preparation and submission of clinical trial-related documentation to regulatory agencies and ethics committees. Develop and implement clinical trial processes, including risk management strategies, monitoring plans, and quality assurance initiatives. Track and report on clinical trial progress, identifying and addressing any issues or risks that could impact trial milestones. Act as a liaison between external vendors, sites, and LifeMine leadership to ensure effective communication and timely decision-making. Stay up-to-date with industry trends, regulatory changes, and clinical trial best practices to drive continuous improvement within the organization. What you will need to be successful: Bachelor’s or Master’s degree in Life Sciences or a related field Minimum of 3 (Manager)/ 5 (Sr. Manager) years of experience in clinical operations within the pharmaceutical or biotechnology industry. Strong knowledge of clinical trial design, execution, and regulatory requirements (FDA, EMA, ICH-GCP). Proven track record of managing multi-site, complex clinical trials from start-up to completion. Experience working with CROs, vendors, and clinical trial sites, including contract negotiation and performance oversight. Excellent organizational, leadership, and communication skills with the ability to manage cross-functional teams effectively. Strong problem-solving skills, with the ability to identify and address challenges in a fast-paced, dynamic environment. Ability to manage multiple priorities and deadlines, while maintaining a high level of attention to detail. Proficiency in clinical trial management systems (CTMS) and other relevant software tools. Ability to travel as needed for site visits, meetings, and other clinical operations activities.", "summaryDescription" : "Manager/Sr. Manager, Clinical Operations at LifeMine Therapeutics. Skills: Clinical operations management, Clinical trial execution, Vendor management. Manage clinical trials execution. Provide strategic oversight", "postedDate" : "2026-06-14T21:46:00.628", "createdAt" : "2026-06-14T21:46:00.628", "lastUpdated" : "2026-06-16T01:29:08.969", "ingestTimestamp" : "2026-06-14T21:46:00.628", "mongoId" : "6a2c6a8f74d8ee00a090c9c7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 155000, "salaryAnnualMax" : 215000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Clinical trial design", "Clinical trial execution", "Regulatory requirements", "Leadership", "Problem-solving", "Clinical operations management", "Vendor management", "Contract negotiation", "Performance oversight", "Clinical trial management", "Good Clinical Practices", "GCP", "FDA", "EMA", "ICH-GCP", "Clinical development lifecycle" ], "skillCount" : 16, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 0.8888889, "_score" : 503.98798, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.97 }, { "id" : "6a2c5e6674d8ee00a08e3c39", "title" : "Senior Clinical Trial Manager (Atopic Dermatitis)", "company" : "Beeline Medicines", "industry" : "Biotechnology", "salary" : { "min" : 155000.0, "max" : 210000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for Senior Clinical Trial Manager in the United States, adjusted for seniority, biotech industry, and onsite work mode." }, "location" : "United States", "locations" : [ "United States" ], "timestamp" : "2026-06-14T22:32:57.002", "fingerprint" : "a35cfe15fba26397cd8be64a2a4781d08f0a0c83e1df9791ef2a580edb484487", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/beelinemedicines/jobs/4247424009", "externalId" : "4247424009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chicago", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.8755616,-87.6244212" }, { "city" : "Tel Aviv", "country" : "Israel", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "32.0852997,34.7818064" }, { "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "Chicago, Illinois, United States; Tel Aviv, Israel; United States", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "CTMS, EDC, eTMF, Risk-based monitoring", "professionalSkills" : [ "Clinical trial management", "Operational planning", "Regulatory standards", "GCP compliance", "SOP compliance", "Protocol development", "CRF design", "ICF review", "Operational study plans", "Data collection", "Database lock", "Regulatory filings", "Inspection readiness", "Audit preparation" ], "hardSkillsList" : [ "Clinical operations", "Global clinical trials", "Immunology indications", "Autoimmune diseases", "Inflammatory diseases", "Biologics", "Monoclonal antibodies", "Advanced therapies", "Clinical trial regulations", "Operational best practices", "Pivotal trials" ], "softSkillsList" : [ "Leadership", "Problem-solving" ], "hardSkills" : [ { "name" : "Clinical operations", "level" : "intermediate" }, { "name" : "Global clinical trials", "level" : "intermediate" }, { "name" : "Immunology indications", "level" : "intermediate" }, { "name" : "Autoimmune diseases", "level" : "intermediate" }, { "name" : "Inflammatory diseases", "level" : "intermediate" }, { "name" : "Biologics", "level" : "intermediate" }, { "name" : "Monoclonal antibodies", "level" : "intermediate" }, { "name" : "Advanced therapies", "level" : "intermediate" }, { "name" : "Clinical trial regulations", "level" : "intermediate" }, { "name" : "Operational best practices", "level" : "intermediate" }, { "name" : "Pivotal trials", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Problem-solving" } ], "majorSkills" : "Clinical trial management, Immunology, Autoimmune diseases", "majorSkillsList" : [ "Clinical trial management", "Immunology", "Autoimmune diseases" ], "coreResponsibilities" : "Lead operational strategy, Plan clinical trials, Execute clinical trials, Oversee clinical trials, Serve as primary operational point of contact, Oversee selection of CROs, Manage CROs, Oversee vendor selection, Manage vendors, Drive site feasibility, Drive site selection, Drive site activation, Drive patient recruitment strategies, Manage ongoing site management, Develop study timelines, Maintain study timelines, Develop risk mitigation strategies, Maintain risk mitigation strategies, Develop operational tracking tools, Maintain operational tracking tools, Collaborate on protocol development, Collaborate on CRF design, Collaborate on ICF review, Collaborate on operational study plans, Ensure studies compliance, Identify operational issues, Resolve operational issues, Escalate risks, Implement mitigation strategies, Oversee data collection activities, Oversee database lock readiness, Support data review processes, Contribute to regulatory filings, Contribute to inspection readiness, Contribute to audit preparation, Provide leadership to team members, Provide mentorship to team members, Contribute to process improvement initiatives", "teamCollaboration" : "Internal cross-functional teams; External partners; CROs; Vendors; Sites; Clinical Operations team members", "projectManagementSkills" : [ "Clinical trial management", "Risk mitigation", "Timeline management" ], "domainKnowledge" : "Immunology; Autoimmune diseases; Inflammatory diseases; Biologics; Monoclonal antibodies; Advanced therapies; GCP; ICH guidelines; Clinical trial regulations", "domainList" : [ "immunology", "autoimmune-diseases", "inflammatory-diseases", "biologics", "monoclonal-antibodies", "advanced-therapies", "gcp", "ich-guidelines", "clinical-trial-regulations" ], "domainSpecificKnowledge" : [ "Immunology", "Autoimmune diseases", "Inflammatory diseases", "Biologics", "Monoclonal antibodies", "Advanced therapies", "GCP", "ICH guidelines", "Clinical trial regulations" ], "toolProficiency" : [ "CTMS", "EDC", "eTMF", "Risk-based monitoring tools" ], "documentationSkills" : "Protocol development; CRF design; ICF review; Operational study plans; Regulatory filings", "problemSolvingSkills" : "Problem-solving; Risk mitigation; Issue resolution", "specialRequirements" : "Travel up to 20%, Domestic travel, International travel, Overnight stays, Availability during Eastern Time", "outcomesObjectives" : "Ensure studies delivered on time; Ensure studies within scope; Ensure studies compliance; Achieve enrollment goals", "qualificationsBasic" : "Bachelor's degree in life sciences, Minimum 5 years of experience in clinical operations, At least 3 years in a Senior CTM role, Proven track record of managing global clinical trials, Experience with biologics, Knowledge of GCP/ICH guidelines, Experience in early- to late-stage development programs", "qualificationsPreferred" : "Advanced degree preferred, Experience in rare autoimmune indications, Familiarity with adaptive trial designs, Experience with complex biomarker-driven studies", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully. Job Summary: The Senior Clinical Trial Manager (Sr. CTM) will lead the operational planning, execution, and oversight of complex, global clinical studies in the field of immunology and autoimmune diseases. This role is responsible for ensuring studies are delivered on time, within scope, and in compliance with regulatory standards, Good Clinical Practice (GCP), and company Standard Operating Procedures (SOPs). The Sr. CTM will partner closely with internal cross-functional teams (Clinical Development, Regulatory, Biometrics, Safety, and Quality) and external partners (CROs, vendors, and sites) to ensure operational excellence. This individual will also play a critical role in driving strategic decision-making and supporting inspection readiness and regulatory submissions. Work Arrangement the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company's discretion based on business need. Essential Duties and Responsibilities: Lead the operational strategy, planning, and execution of global Phase 1–4 clinical trials in immunology indications (e.g., autoimmune and inflammatory diseases). Serve as the primary operational point of contact for internal stakeholders and external partners. Oversee the selection and management of CROs and other vendors, including scope of work, budget development, contracting, and performance oversight. Drive site feasibility, site selection, activation, patient recruitment strategies, and ongoing site management to ensure achievement of enrollment goals. Develop and maintain study timelines, risk mitigation strategies, and operational tracking tools. Collaborate with cross-functional teams on protocol development, CRF design, ICF review, and development of operational study plans. Ensure studies are conducted in compliance with GCP/ICH guidelines, local regulatory requirements, and internal SOPs. Proactively identify and resolve operational issues, escalating risks and implementing mitigation strategies as needed. Oversee data collection activities, database lock readiness, and support data review processes. Contribute to regulatory filings, inspection readiness, and audit preparation. Provide leadership and mentorship to Clinical Operations team members. Contribute to process improvement initiatives within Clinical Operations to enhance efficiency and quality. Perform other duties and responsibilities as assigned Qualifications: Education: Bachelor’s degree in life sciences or related field (advanced degree preferred) Minimum 5 years of experience in clinical operations in the biopharmaceutical industry, with at least 3 years in a Senior CTM or equivalent leadership role. Proven track record of managing global, multi-center clinical trials in immunology or autoimmune disease indications. Experience with biologics, monoclonal antibodies, or advanced therapies. Strong knowledge of GCP/ICH guidelines, clinical trial regulations, and operational best practices. Experience in rare autoimmune indications or immune-mediated inflammatory diseases. Familiarity with adaptive trial designs or complex biomarker-driven studies. Experience in early- to late-stage development programs, including pivotal trials. Proficiency with electronic systems such as CTMS, EDC, eTMF, and risk-based monitoring tools. Ability to thrive in a fast-paced, dynamic environment and work independently with minimal supervision Excellent communication, leadership, and problem-solving skills. This position requires availability during Eastern Time (ET) business hours This role may require domestic and international travel, including overnight stays, up to 20% or more based on business needs Salary Range: The expected annual salary range for this position is listed below. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance. Salary Range $178,000—$194,500 USD Benefits: We offer a comprehensive benefits package including: Medical, Dental & Vision insurance (employee premiums 100% covered by company) 20 accrued days combined time off (PTO/Sick), 12 company holidays, & winter recharge Flexible work arrangements / hybrid schedule Health Savings Account (HSA) *Benefits are subject to eligibility requirements and plan terms. Additional details provided during the offer process* Equal Employment Opportunity: Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. Reasonable Accommodation: If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates. Privacy Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at Privacy Policy - Beeline Medicines", "summaryDescription" : "Senior Clinical Trial Manager (Atopic Dermatitis) at Beeline Medicines. Skills: Clinical trial management, Immunology, Autoimmune diseases. Lead operational strategy. Plan clinical trials", "postedDate" : "2026-06-12T22:01:31.594", "createdAt" : "2026-06-12T22:01:31.594", "lastUpdated" : "2026-06-14T22:32:57.002", "ingestTimestamp" : "2026-06-12T22:01:31.594", "mongoId" : "6a2c5e6674d8ee00a08e3c39", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 155000, "salaryAnnualMax" : 210000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Clinical operations", "Global clinical trials", "Immunology indications", "Autoimmune diseases", "Inflammatory diseases", "Biologics", "Monoclonal antibodies", "Advanced therapies", "Clinical trial regulations", "Operational best practices", "Pivotal trials", "Leadership", "Problem-solving", "Clinical trial management", "Immunology", "Operational planning", "Regulatory standards", "GCP compliance", "SOP compliance", "Protocol development", "CRF design", "ICF review", "Operational study plans", "Data collection", "Database lock", "Regulatory filings", "Inspection readiness", "Audit preparation", "Risk mitigation", "Timeline management", "GCP", "ICH guidelines", "CTMS", "EDC", "eTMF", "Risk-based monitoring tools" ], "skillCount" : 36, "jobCategory" : "operations", "jobSubcategory" : "clinical-operations", "dataQualityScore" : 0.8888889, "_score" : 503.4244, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a305a14f292fd229cf4d11a", "title" : "Bilingual Clinical Scheduling Assistant", "industry" : "Healthcare", "salary" : { "min" : 38000.0, "max" : 48000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Bilingual Clinical Scheduling Assistant in Houston, TX, adjusted for the healthcare industry." }, "location" : "Houston, TX", "locations" : [ "Houston, TX" ], "timestamp" : "2026-06-16T08:56:06.254", "fingerprint" : "03e25f04d14289c934994e02c109e395e6421e651ea00a9714f4833f0f9c07b6", "source" : "jazzhr", "language" : "en", "externalId" : "tJsJoJ3Eil", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Houston", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "29.7589382,-95.3676974" } ], "locationText" : "Houston, Texas, United States", "coreResponsibilities" : "Schedule patient appointments, Manage provider schedules, Coordinate patient care, Handle patient inquiries, Maintain patient records, Process patient intake, Assist with administrative tasks", "domainKnowledge" : "Clinical scheduling", "domainList" : [ "clinical-scheduling" ], "domainSpecificKnowledge" : [ "Clinical scheduling" ], "documentationSkills" : "Patient records", "qualificationsBasic" : "Bilingual in Spanish and English", "workSiteFlexibility" : "Onsite", "summaryDescription" : "Bilingual Clinical Scheduling Assistant. Schedule patient appointments. Manage provider schedules", "createdAt" : "2026-06-15T22:22:24.330", "lastUpdated" : "2026-06-16T08:56:06.254", "ingestTimestamp" : "2026-06-15T22:22:24.330", "mongoId" : "6a305a14f292fd229cf4d11a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 38000, "salaryAnnualMax" : 48000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Clinical scheduling" ], "skillCount" : 1, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.44444445, "_score" : 499.18222, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.9 }, { "id" : "6a305a14f292fd229cf4d119", "title" : "Bilingual Clinical Scheduling Assistant", "industry" : "Healthcare", "salary" : { "min" : 38000.0, "max" : 52000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Bilingual Clinical Scheduling Assistant in Houston, TX, adjusted for the healthcare industry." }, "location" : "Houston, TX", "locations" : [ "Houston, TX" ], "timestamp" : "2026-06-16T07:22:53.752", "fingerprint" : "9165841a69b949f3d0d16d6833e60050551c650a30a8fd64717d3c3771064438", "source" : "jazzhr", "language" : "en", "externalId" : "ilYenVgeMw", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Houston", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "29.7589382,-95.3676974" } ], "locationText" : "Houston, Texas, United States", "coreResponsibilities" : "Schedule patient appointments, Manage provider schedules, Coordinate patient care, Handle patient inquiries, Maintain patient records, Process patient intake, Verify insurance information, Assist with administrative tasks", "teamCollaboration" : "Coordinate with clinical staff; Liaise with external providers", "domainKnowledge" : "Clinical scheduling; Medical terminology", "domainList" : [ "clinical-scheduling", "medical-terminology" ], "domainSpecificKnowledge" : [ "Clinical scheduling", "Medical terminology" ], "communicationSkills" : "Patient communication", "documentationSkills" : "Patient records", "qualificationsBasic" : "Bilingual in Spanish and English", "workSiteFlexibility" : "Onsite", "summaryDescription" : "Bilingual Clinical Scheduling Assistant. Schedule patient appointments. Manage provider schedules", "createdAt" : "2026-06-15T22:21:58.125", "lastUpdated" : "2026-06-16T07:22:53.752", "ingestTimestamp" : "2026-06-15T22:21:58.125", "mongoId" : "6a305a14f292fd229cf4d119", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 38000, "salaryAnnualMax" : 52000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Clinical scheduling", "Medical terminology" ], "skillCount" : 2, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.44444445, "_score" : 499.1641, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.92 }, { "id" : "6a1a5df558b93c861e811cff", "title" : "Clinical Assistant 2", "industry" : "Healthcare", "salary" : { "min" : 33000.0, "max" : 45000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Entry level Clinical Assistant 2 in Bayonet Point, United States, adjusted for the healthcare industry." }, "location" : "United States-Florida-Bayonet Point", "locations" : [ "United States-Florida-Bayonet Point", "
TGHI Bayonet (TGHIBAYON)
7525 State Route 52
Bayonet Point, 34667

" ], "certifications" : [ "CPR certification", "Certified M. A", "IV certification" ], "timestamp" : "2026-06-16T06:45:47.761", "fingerprint" : "c17ffb96437361128240f37161ea4cf9e0d00a5b9494f6da4ed38e1d117276b7", "source" : "taleo", "language" : "en", "applyUrl" : "https://tas-tgh.taleo.net/careersection/ex/jobdetail.ftl?job=671907", "externalId" : "671907", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bayonet Point", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "28.3251795,-82.6826570" } ], "locationText" : "Bayonet Point, Florida, United States", "minimumEducation" : "High School", "experienceMinYears" : 1, "technicalSkills" : "RIS, PACS", "professionalSkills" : [ "Patient history taking", "Procedure explanation", "Vital signs measurement", "Medical records software" ], "hardSkillsList" : [ "Contrast administration", "Injection administration", "IV insertion" ], "hardSkills" : [ { "name" : "Contrast administration", "level" : "intermediate" }, { "name" : "Injection administration", "level" : "intermediate" }, { "name" : "IV insertion", "level" : "intermediate" } ], "majorSkills" : "Patient preparation, Clinical assistance, Radiology procedures", "majorSkillsList" : [ "Patient preparation", "Clinical assistance", "Radiology procedures" ], "coreResponsibilities" : "Confirm patient appointments, Perform pre-screening interview, Interview patients, Measure vital signs, Record patient information, Prepare patient for exam, Prepare treatment room, Prepare trays for examination, Administer contrast, Administer injections, Assist with IV, Seek past images for patients, Call reports to physician's office, Stock supplies, Order supplies, Fax reports", "teamCollaboration" : "Cooperative relationships with patients; Cooperative relationships with families; Cooperative relationships with physicians; Cooperative relationships with staff", "domainKnowledge" : "Radiology; Imaging office procedures", "domainList" : [ "radiology", "imaging-office-procedures" ], "domainSpecificKnowledge" : [ "Radiology", "Imaging office procedures" ], "toolProficiency" : [ "Medical records software", "RIS", "PACS" ], "communicationSkills" : "Clear communication", "documentationSkills" : "Record patient information", "qualificationsBasic" : "High school diploma or equivalent, Current CPR certification, Minimum of one-year work experience in public contact job, Basic knowledge of radiology and imaging office procedures, Skill in using computer and medical records software and RIS/PACS competently, Ability to communicate clearly in person and over the phone", "qualificationsPreferred" : "Certified M. A. preferred, IV certification preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Summary: Responsible for administrative as well as clinical tasks. Assists in preparing the patient and the room for procedures under the direction of the technologist or radiologist. Takes patient history, explains procedure, give out contrast, injections, and place IVs for contrast injections. Essential Duties and Responsibilities: Calls patients to confirm appointments and performs a pre-screening interview with the patient before their appointment date. Interviews patients, measures vital signs, such as pulse rate, temperature, blood pressure, weight and records information in patients’ file. Prepares patient for exam (changing into gown, removing all metal). Prepares treatment room and trays for examination. Administers contrast, injections and assists with IV when needed. Seeks past images for patients who have them or are needed. Call reports to the referring physician’s office, when requested. Stock/order supplies, fax reports, and any other duties that may be assigned daily. Required Qualifications / Education / Experience: High school diploma or equivalent. Certified M.A. preferred. IV certification preferred. Current CPR certification. Minimum of one-year work experience in public contact job, preferably service related. Basic knowledge of radiology and imaging office procedures. Skill in using computer and medical records software and RIS/PACS competently to process patient images and department information. Ability to communicate clearly in person and over the phone to establish/maintain cooperative relationships with patients, families, physicians and other staff. Bayonet Point", "summaryDescription" : "Clinical Assistant 2. Skills: Patient preparation, Clinical assistance, Radiology procedures. Confirm patient appointments. 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A", "IV certification", "RIS", "PACS" ], "skillCount" : 17, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Entry", "dataQualityScore" : 0.5555556, "_score" : 488.42133, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2d8c0474d8ee00a0c2c870", "title" : "Clinique Counter Manager", "company" : "Clinique", "industry" : "Retail", "salary" : { "min" : 55000.0, "max" : 75000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Retail Counter Manager in Raleigh, United States, adjusted for seniority and company size." }, "location" : "Raleigh, NC - Crabtree Valley Mall Belk", "locations" : [ "Raleigh, NC - Crabtree Valley Mall Belk", "United States of America" ], "certifications" : [ "Professional licenses", "Demonstrator licenses", "Cosmetology licenses" ], "timestamp" : "2026-06-15T21:57:08.413", "fingerprint" : "461d62d9c5e7f7857ce2479b2e0209fae0053a05194d46fcf4a9275f900483cd", "source" : "workday", "language" : "en", "applyUrl" : "https://belk.wd1.myworkdayjobs.com/Jobs-Stores/job/Raleigh-NC---Crabtree-Valley-Mall-Belk/Clinique-Counter-Manager---Full-Time---Crabtree-Mall_JR-102160", "externalId" : "JR-102160", "industryFunction" : { }, "locationPoint" : "-30.43957,152.97115", "structuredLocations" : [ { "city" : "Raleigh", "state" : "North Carolina", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.7803977,-78.6390989" } ], "locationText" : "Raleigh, North Carolina, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "technicalSkills" : "Windows-based operating systems", "professionalSkills" : [ "Selling behaviors", "Selling strategies", "Customer outreach", "Visual merchandising", "Inventory management", "Asset protection" ], "hardSkillsList" : [ "Product knowledge", "Artistry skills", "Beauty trends", "Selling skills", "Omni processes", "Merchandising product", "Replenishment", "Recovery", "Cleanliness", "Price changes", "Product transfers", "Damaged items processing" ], "softSkillsList" : [ "Adaptability" ], "hardSkills" : [ { "name" : "Product knowledge", "level" : "intermediate" }, { "name" : "Artistry skills", "level" : "intermediate" }, { "name" : "Beauty trends", "level" : "intermediate" }, { "name" : "Selling skills", "level" : "intermediate" }, { "name" : "Omni processes", "level" : "intermediate" }, { "name" : "Merchandising product", "level" : "intermediate" }, { "name" : "Replenishment", "level" : "intermediate" }, { "name" : "Recovery", "level" : "intermediate" }, { "name" : "Cleanliness", "level" : "intermediate" }, { "name" : "Price changes", "level" : "intermediate" }, { "name" : "Product transfers", "level" : "intermediate" }, { "name" : "Damaged items processing", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Adaptability" } ], "majorSkills" : "Sales, Client relationships, Team leadership", "majorSkillsList" : [ "Sales", "Client relationships", "Team leadership" ], "coreResponsibilities" : "Achieve store objectives, Drive personal key metrics, Drive store key metrics, Create memorable store experiences, Build team relationships, Build vendor relationships, Build customer relationships, Build community relationships, Lead team in providing excellent customer service, Drive sales, Achieve goals, Execute successful promotions, Execute special events, Execute customer outreach, Advance beauty business, Foster a positive store culture, Share team successes, Celebrate associate achievements, Model behaviors that strengthen performance, Model behaviors that enhance customer service, Build personal product knowledge, Build team product knowledge, Build personal suggestive selling behaviors, Build team suggestive selling behaviors, Build personal artistry skills, Build team artistry skills, Build personal expertise in beauty trends, Build team expertise in beauty trends, Create exciting customer engagement, Drive repeat client interactions, Assist with onboarding, Initiate teaching opportunities, Support associate continued learning, Connect with Beauty Advisors, Review goals, Review performance results, Ensure associates are well-informed, Ensure associates are confident speaking to inventory, Leverage clienteling tools, Leverage technology, Provide a personalized omnichannel experience, Provide a seamless omnichannel experience, Support store fulfillment, Execute omni processes, Support team with merchandising product, Support team with replenishment, Support team with recovery, Support team with cleanliness, Maintain visual merchandising standards, Maintain beauty hygiene standards, Align presentations with vendor directives, Align presentations with company directives, Partner with store leaders, Ensure team schedules align with business needs, Ensure team schedules align with traffic plans, Ensure team schedules align with event strategies, Maximize associate productivity, Maximize department productivity, Respond to changing circumstances, Adjust tactics, Shift focus based on evolving business needs, Lead shortage control, Lead inventory accuracy, Execute price changes, Execute product transfers, Process damaged items timely, Champion team knowledge of inventory management, Champion team knowledge of asset protection procedures, Champion team knowledge of safety guidelines", "teamCollaboration" : "Team meetings; One-on-one touch bases; Partner with store leaders", "domainKnowledge" : "Cosmetic trends; Beauty trends; Fragrance trends", "domainList" : [ "cosmetic-trends", "beauty-trends", "fragrance-trends" ], "domainSpecificKnowledge" : [ "Cosmetic trends", "Beauty trends", "Fragrance trends" ], "toolProficiency" : [ "Clienteling tools", "Technology" ], "communicationSkills" : "Communicate with excellence", "continuousLearning" : "Commitment to continuously learn", "problemSolvingSkills" : "Timely and effective decisions", "specialRequirements" : "Must regularly move around all store areas, Must bend, reach, stretch for product, Must lift, carry, and move at least 40 lbs", "outcomesObjectives" : "Achieving store objectives; Driving accomplishment of personal key metrics; Driving accomplishment of store key metrics", "qualificationsBasic" : "1+ years of retail experience, Available to work a flexible schedule, Must regularly move around all store areas, Must bend, reach, stretch for product, Must lift, carry, and move at least 40 lbs, Comfortable with assisting customers with makeup application, Comfortable with assisting customers with skincare services, Maintain all required professional licenses and certifications", "qualificationsPreferred" : "Cosmetology licenses as required", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "The Beauty Counter Manager drives personal and team results within an assigned brand, demonstrating a passion for building personalized client relationships and sharing a genuine enthusiasm for cosmetic, beauty, and fragrance trends. This role utilizes engaging selling behaviors and strategies to enhance customer experience, while executing promotions, special events, and customer outreach initiatives. The Beauty Counter Manager possesses a competitive drive and entrepreneurial confidence to excel in a fast-paced commission environment. This is an hourly position, with monthly bonus eligibility. **What you will do** * Demonstrate a high level of ownership, accountability, and initiative in achieving store objectives and driving the accomplishment of personal and store key metrics. * Create memorable store experiences through building genuine team, vendor, customer, and community relationships. * Lead team in providing excellent customer service, driving sales, achieving goals, and executing successful promotions, special events, and customer outreach to advance beauty business. Foster a positive store culture by sharing team successes, celebrating associate achievements, and modeling behaviors that strengthen performance and enhance customer service. * Build personal and team product knowledge, suggestive selling behaviors, artistry skills, and expertise in the latest industry tips and beauty trends to create exciting customer engagement. Drive repeat client interactions as a knowledgeable and trusted resource. * Enhance team’s selling skills by assisting with onboarding, initiating teaching opportunities, and supporting associate continued learning. Connect with Beauty Advisors through team meetings and one-on-one touch bases to review goals and performance results. * Ensure associates are well-informed and confident in speaking to available inventory and assortment. Leverage clienteling tools and technology to provide a personalized and seamless omnichannel experience. Support store fulfillment in designated areas by accurately and efficiently executing omni processes. * Support team with merchandising product, replenishment, recovery, and cleanliness to maintain visual merchandising and beauty hygiene standards daily. Align presentations with vendor and company directives. * Partner with store leaders to ensure team schedules align with business needs, traffic plans, and event strategies to maximize associate and department productivity. * Demonstrate adaptability and respond to changing circumstances, adjusting tactics and shifting focus based on evolving business needs. * Lead shortage control and inventory accuracy in designated areas by executing price changes, product transfers, and processing damaged items timely. Champion team knowledge of inventory management, asset protection procedures, and safety guidelines. **Skills and Abilitie****s** * Ability to use data, guidance, and judgement to support timely and effective decisions that contribute to team and business success. * Skills and experience to perform in the role and a commitment to continuously learn. * Ability to take ownership of assigned tasks and contribute to store success by teaching, partnering, and encouraging others. * Self-directed and able to work with minimal supervision in a deadline-driven environment. * Communicate with excellence. * Comfortable with technology, including smart phones, tablet computers and Windows-based operating systems. * 1+ years of retail experience and a dedication to customer service excellence. * Available to work a flexible schedule based on business needs, including nights, weekends, and holidays. * Must regularly move around all store areas and be accessible to customers. * Must bend, reach, stretch for product as well as lift, carry, and move at least 40 lbs. * Comfortable with and enjoy assisting customers with makeup application and skincare services. * Associates must maintain all required professional licenses and certifications, including any state-specific demonstrator or cosmetology licenses, as required by applicable state and local regulatory boards. The job posting highlights the most relevant / essential responsibilities and requirements of the role. It is not all-inclusive. There may be additional duties, responsibilities, and qualifications for this job.", "summaryDescription" : "Clinique Counter Manager at Clinique. Skills: Sales, Client relationships, Team leadership. Achieve store objectives. Drive personal key metrics", "postedDate" : "2026-06-13T18:54:48.423", "createdAt" : "2026-06-14T18:54:48.413", "lastUpdated" : "2026-06-15T21:57:08.413", "ingestTimestamp" : "2026-06-14T18:54:48.413", "mongoId" : "6a2d8c0474d8ee00a0c2c870", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://belk.wd1.myworkdayjobs.com/Jobs-Stores/job/Raleigh-NC---Crabtree-Valley-Mall-Belk/Clinique-Counter-Manager---Full-Time---Crabtree-Mall_JR-102160", "salaryAnnualMin" : 55000, "salaryAnnualMax" : 75000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Product knowledge", "Artistry skills", "Beauty trends", "Selling skills", "Omni processes", "Merchandising product", "Replenishment", "Recovery", "Cleanliness", "Price changes", "Product transfers", "Damaged items processing", "Adaptability", "Sales", "Client relationships", "Team leadership", "Selling behaviors", "Selling strategies", "Customer outreach", "Visual merchandising", "Inventory management", "Asset protection", "Cosmetic trends", "Fragrance trends", "Professional licenses", "Demonstrator licenses", "Cosmetology licenses", "Clienteling tools", "Technology" ], "skillCount" : 29, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "manager", "dataQualityScore" : 1.0, "_score" : 483.14395, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Retail", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a3fb574d8ee00a05c465e", "title" : "Clinical Trial Manager", "company" : "Precision Medicine Group", "industry" : "Life Sciences", "salary" : { "min" : 450000.0, "max" : 750000.0, "currency" : "CNY", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Clinical Trial Manager in China, adjusted for the biotech industry and remote work." }, "location" : "Remote (China)", "locations" : [ "Remote (China)" ], "timestamp" : "2026-06-11T07:50:44.742", "fingerprint" : "3ad6e88d5e1e9a20fe8ae8193933eaf0afc10f8db376a2ecc84f38f979c36fd7", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/precisionmedicinegroup/jobs/6016951004", "externalId" : "6016951004", "industryFunction" : { }, "structuredLocations" : [ { "country" : "China", "continent" : "as", "workMode" : "remote" } ], "locationText" : "China", "experienceLevel" : "Manager", "professionalSkills" : [ "Clinical trial execution", "Scientific knowledge", "Laboratory expertise", "Data sciences" ], "hardSkillsList" : [ "Clinical monitoring", "Protocol development", "Regulatory requirements", "Site feasibility", "Enrollment strategy", "Vendor management", "Data quality", "Data cleaning" ], "hardSkills" : [ { "name" : "Clinical monitoring", "level" : "intermediate" }, { "name" : "Protocol development", "level" : "intermediate" }, { "name" : "Regulatory requirements", "level" : "intermediate" }, { "name" : "Site feasibility", "level" : "intermediate" }, { "name" : "Enrollment strategy", "level" : "intermediate" }, { "name" : "Vendor management", "level" : "intermediate" }, { "name" : "Data quality", "level" : "intermediate" }, { "name" : "Data cleaning", "level" : "intermediate" } ], "majorSkills" : "Clinical trial management, Protocol adherence, Regulatory compliance", "majorSkillsList" : [ "Clinical trial management", "Protocol adherence", "Regulatory compliance" ], "coreResponsibilities" : "Serve as clinical trial lead, Plan clinical studies, Conduct clinical studies, Oversee clinical studies, Ensure protocol adherence, Ensure SOP adherence, Ensure GCP adherence, Ensure regulatory adherence, Act as primary clinical point of contact, Collaborate on invoicing, Manage clinical budget variance, Develop study related documents, Identify training needs for CRAs, Identify training needs for vendors, Present at Investigator Meetings, Present at Study Kick-off meetings, Generate potential site list, Drive site feasibility process, Identify risks to enrollment targets, Develop country recruitment strategy, Develop country retention strategy, Develop communication with investigators, Develop relationships with investigators, Ensure effective site feasibility, Ensure effective site start up, Ensure effective enrollment, Ensure effective site maintenance, Ensure effective site close out, Lead internal clinical team meetings, Set expectations for clinical team, Address CRA questions, Address site questions, Maintain FAQ log, Support investigator meetings, Review IP release packages, Approve IP release packages, Oversee submissions to Competent Authorities, Oversee approvals to Competent Authorities, Oversee submissions to IRB/Ethics Committees, Oversee approvals to IRB/Ethics Committees, Develop clinical monitoring strategies, Assure study timelines are met, Assure quality deliverables, Generate metric reporting, Utilize metric reporting, Ensure study is conducted per plan, Communicate issues to PM, Communicate issues to CRAs, Implement eTMF, Manage eTMF, Develop CAPA, Implement CAPA, Close CAPA, Assist sites with GCP audits, Assist internal staff with GCP audits, Assist CRAs with GCP audits, Address project-specific resourcing issues, Escalate CRA performance issues, Escalate site compliance issues, Ensure data quality, Ensure compliance with data cleaning timelines, Manage investigational product processes, Manage drug accountability, Manage drug reconciliation, Assume project management responsibility, Support business development activities, Support marketing activities, Negotiate site budget, Negotiate investigator contract, Review site visit reports, Ensure monitoring is executed per plan, Manage clinical vendors, Perform clinical data review, Generate query, Manage workload of supervised staff, Perform other duties as assigned", "teamCollaboration" : "Internal clinical team; CRAs; CTAs; Data management; QA; Regulatory departments; Legal department; Site contracts group", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Oncology; Rare Disease; ICH-GCP; Clinical trial monitoring; Clinical documentation; Investigational product", "domainList" : [ "oncology", "rare-disease", "ich-gcp", "clinical-trial-monitoring", "clinical-documentation", "investigational-product" ], "domainSpecificKnowledge" : [ "Oncology", "Rare Disease", "ICH-GCP", "Clinical trial monitoring", "Clinical documentation", "Investigational product" ], "toolProficiency" : [ "CTMS", "eTMF" ], "communicationSkills" : "Presenting at meetings", "documentationSkills" : "Clinical documents; CRF completion guidelines; Study trackers; Training materials; FAQ log", "problemSolvingSkills" : "Risk identification; Problem resolution", "qualificationsBasic" : "Bachelor's degree or equivalent, 5-8 years clinical research experience, Significant clinical monitoring experience", "qualificationsPreferred" : "Advanced degree preferred, Oncology (Phase I) trial experience in Taiwan and China preferred", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease. We are hiring for a Clinical Trial Manager (based in Shanghai/Beijing) Position Summary: Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies per defined scope of work and ensures that clinical studies are conducted in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP and all applicable regulatory requirements. Essential functions of the job include but are not limited to: Primary clinical point of contact with the client Collaborate with PM on monthly invoicing and variance management of clinical budget Develop study related clinical documents (e. g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials) Identify and develop training needs for CRAs and third-party vendors specific to the study, protocol and practices including presenting these at Investigator Meetings and Study Kick-off meetings Generate potential site list from key stakeholders and drive site feasibility process Identify potential risks to the enrollment targets based on feasibility analysis and site’s contracted commitment Develop and finalize the country recruitment/retention strategy Develop timely and effective communication and good working relationships with investigators and study team to ensure effective and timely feasibility, site start up, enrollment, maintenance and close out procedures Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs Address all CRA and site questions and maintains Frequently Asked Question (FAQ) log as appropriate Support in planning and conducting investigator meetings Review and/or approve of IP release packages Oversee, support and track all submissions and approvals to Competent Authorities and IRB/Ethics Committees in conjunction with regulatory departments as applicable Develop clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables Generate and utilize metric reporting (e. g. CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicates issues to PM and CRAs as appropriate Responsible for eTMF implementation and management Collaborate with PM, CRAs and QA to develop any Corrective and Preventative Action Plan (CAPA) and is accountable for implementation and timely closure Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits Work closely with PM for project-specific resourcing issues Escalate pertinent CRA performance and site compliance issues when necessary Collaborate with data management and CRAs to ensure data quality and compliance with data cleaning timelines Manage processes for investigational product (IP) including drug accountability and reconciliation When a cross-functional PM is not assigned to a given program, the CTM will assume project management responsibility as needed Supports business development and marketing activities as appropriate May negotiate site budget and investigator contract with support from the legal department and/or site contracts group May review site visit reports and ensures monitoring (i. e. scheduling and scope) is executed per monitoring plan May be responsible for management of clinical vendors (e. g. labs, IP, patient diary, home health care) in conjunction with PM May perform clinical data review of patient profiles, data listings and summary tables, including query generation May have line management responsibilities May manages workload of supervised staff with continued assessment and adjustment as needed Perform other duties as assigned by management Qualifications: Minimum Required : Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred Minimum of 5-8 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience. Oncology (Phase I) trial experience in Taiwan and China preferred Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.", "summaryDescription" : "Clinical Trial Manager at Precision Medicine Group. Skills: Clinical trial management, Protocol adherence, Regulatory compliance. Serve as clinical trial lead. Plan clinical studies", "postedDate" : "2026-06-11T07:12:27.383", "createdAt" : "2026-06-11T07:12:27.383", "lastUpdated" : "2026-06-11T07:50:44.742", "ingestTimestamp" : "2026-06-11T07:12:27.383", "mongoId" : "6a2a3fb574d8ee00a05c465e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Clinical monitoring", "Protocol development", "Regulatory requirements", "Site feasibility", "Enrollment strategy", "Vendor management", "Data quality", "Data cleaning", "Clinical trial management", "Protocol adherence", "Regulatory compliance", "Clinical trial execution", "Scientific knowledge", "Laboratory expertise", "Data sciences", "Project management", "Oncology", "Rare Disease", "ICH-GCP", "Clinical trial monitoring", "Clinical documentation", "Investigational product", "CTMS", "eTMF" ], "skillCount" : 24, "jobCategory" : "other", "jobSubcategory" : "clinical-solutions", "dataQualityScore" : 0.8888889, "_score" : 481.34732, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Life Sciences" }, { "id" : "6a305e6cf292fd229cf70714", "title" : "Data Manager for Clinical Trials", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 75000.0, "max" : 95000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Data Manager in the Biotech industry in Mississauga, Canada, adjusted for full-time employment." }, "location" : "Mississauga, ON, Canada", "locations" : [ "Mississauga", "ON", "Canada" ], "timestamp" : "2026-06-16T10:38:08.200", "fingerprint" : "6402554b421574d37787eca96b7e77665f5c5fc06e87a9482913b5db02c8b408", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000131986259-data-manager-for-clinical-trials", "externalId" : "744000131986259", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Mississauga", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.5884727,-79.6436580" } ], "locationText" : "Mississauga, Ontario, Canada", "employmentType" : "FULL_TIME", "minimumEducation" : "College or University degree", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "technicalSkills" : "SQL, Python, R, Scala, Spark, Dbt, Tableau, Power BI, Looker, Snowflake, BigQuery, Redshift, Databricks, Fivetran, Airflow, Delta Lake, Scikit-learn, TensorFlow, PyTorch, XGBoost, LightGBM, Hugging Face, MLflow, AWS, GCP, Azure", "professionalSkills" : [ "Clinical data management", "Data reconciliation", "Medical coding", "Query management", "Database lock" ], "hardSkillsList" : [ "Statistical analysis", "Regression", "Classification", "Clustering", "Time-series analysis", "A/B testing", "Causal inference" ], "hardSkills" : [ { "name" : "Statistical analysis", "level" : "intermediate" }, { "name" : "Regression", "level" : "intermediate" }, { "name" : "Classification", "level" : "intermediate" }, { "name" : "Clustering", "level" : "intermediate" }, { "name" : "Time-series analysis", "level" : "intermediate" }, { "name" : "A/B testing", "level" : "intermediate" }, { "name" : "Causal inference", "level" : "intermediate" } ], "majorSkills" : "Data management, Clinical trials, Data quality, Database administration", "majorSkillsList" : [ "Data management", "Clinical trials", "Data quality", "Database administration" ], "coreResponsibilities" : "Act as communication line for project teams, Maintain TMF/eTMF, Train Assistant Data Manager, Support study documentation development, Perform user acceptance testing, Manage user access, Review data, Reconcile eCRF/External data, Perform medical coding, Support SAE reconciliation, Manage queries, Enter and QC local lab normal ranges, Perform Study Database Lock activities, QC archival of CRFs, Perform data entry/QC, Report project status, Generate and deliver data listings/Patient profiles, Assist with Database Lock tasks", "teamCollaboration" : "Project teams", "projectManagementSkills" : [ "Project status reporting" ], "domainKnowledge" : "Clinical data management; Medical science; Life science", "domainList" : [ "clinical-data-management", "medical-science", "life-science" ], "domainSpecificKnowledge" : [ "Clinical data management", "Medical science", "Life science" ], "toolProficiency" : [ "TMF", "ETMF" ], "communicationSkills" : "Communication line", "documentationSkills" : "Study documentation; CRF Completion Guidelines; Data Management Plan; Edit Checks Specification; User Access Management Plan; Data Validation Plan; External Data Transfer Agreements; SAE Reconciliation Guidelines; Local Lab Normal Ranges Guidelines; Coding Guidelines", "problemSolvingSkills" : "Query management", "qualificationsBasic" : "College or University degree, Minimum of one year of industry experience, Experience working with clinical or medical data", "qualificationsPreferred" : "PhD preferred, Specific ML framework experience, Cloud platform certs", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,200 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them. 1. Acts as a communication line for project teams regarding clinical data management 2. Maintains TMF/eTMF 3. Trains Assistant Data Manager 4. Is involved in clinical data management activities including, but not limited to: * Supporting development of study documentation (eCRF Requirements, Edit Checks Specification, Data Management Plan, CRF Completion Guidelines, User Access Management Plan, Data Validation Plan, External Data Transfer Agreements, SAE Reconciliation Guidelines, Local Lab Normal Ranges Guidelines, Coding Guidelines where applicable) * User acceptance testing * User access management * Data review * eCRF/External data reconciliation * Medical coding (for staff with medical/Life Science background) * Supporting SAE reconciliation * Query management * Local lab normal ranges entry and QC * Study Database Lock activities * Archival of CRFs QC * Data entry/QC * Project status reporting * Data listings/Patient profiles generation and delivery * Assisting with Database Lock tasks as needed for assigned projects ## Qualifications * College or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities * A minimum of one year of industry experience, preferably working with clinical or medical data", "summaryDescription" : "Data Manager for Clinical Trials at PSI CRO. Skills: Data management, Clinical trials, Data quality, Database administration. Act as communication line for project teams. Maintain TMF/eTMF", "postedDate" : "2026-06-12T20:35:30.000", "createdAt" : "2026-06-16T00:25:49.908", "lastUpdated" : "2026-06-16T10:38:08.200", "ingestTimestamp" : "2026-06-16T00:25:49.908", "mongoId" : "6a305e6cf292fd229cf70714", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Statistical analysis", "Regression", "Classification", "Clustering", "Time-series analysis", "A/B testing", "Causal inference", "Data management", "Clinical trials", "Data quality", "Database administration", "Clinical data management", "Data reconciliation", "Medical coding", "Query management", "Database lock", "Project status reporting", "Medical science", "Life science", "TMF", "ETMF" ], "skillCount" : 21, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 481.0943, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c91e974d8ee00a0984529", "title" : "Senior Counsel (Complex Trial)", "company" : "Tyson & Mendes LLP", "industry" : "Legal", "salary" : { "min" : 160000.0, "max" : 190000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Costa Mesa, California, United States", "locations" : [ "Costa Mesa", "California", "United States" ], "certifications" : [ "Admission to the State Bar" ], "timestamp" : "2026-06-16T05:50:15.234", "fingerprint" : "bfe263799df1be5e4fcb167d2fb4a067cb51102403abc9380646717e916e8f0b", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/tysonmendesllp/jobs/5253958008", "externalId" : "5253958008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Diego", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "32.7174202,-117.1627720" } ], "locationText" : "San Diego, California, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Trial advocacy", "Legal research", "Legal writing", "Case management", "Negotiation", "Pleading drafting", "Discovery management", "Motion practice", "Client counseling", "Deposition preparation", "Witness preparation" ], "hardSkillsList" : [ "Complex trial", "Commercial litigation", "Construction defect", "Employment litigation", "Premises liability", "Product liability", "Catastrophic injury", "Medical malpractice", "Trucking litigation", "Toxic tort", "Professional liability", "Business litigation", "Appeals", "Arbitration", "Mediation" ], "hardSkills" : [ { "name" : "Complex trial", "level" : "intermediate" }, { "name" : "Commercial litigation", "level" : "intermediate" }, { "name" : "Construction defect", "level" : "intermediate" }, { "name" : "Employment litigation", "level" : "intermediate" }, { "name" : "Premises liability", "level" : "intermediate" }, { "name" : "Product liability", "level" : "intermediate" }, { "name" : "Catastrophic injury", "level" : "intermediate" }, { "name" : "Medical malpractice", "level" : "intermediate" }, { "name" : "Trucking litigation", "level" : "intermediate" }, { "name" : "Toxic tort", "level" : "intermediate" }, { "name" : "Professional liability", "level" : "intermediate" }, { "name" : "Business litigation", "level" : "intermediate" }, { "name" : "Appeals", "level" : "intermediate" }, { "name" : "Arbitration", "level" : "intermediate" }, { "name" : "Mediation", "level" : "intermediate" } ], "majorSkills" : "Complex trial, Litigation, Legal analysis", "majorSkillsList" : [ "Complex trial", "Litigation", "Legal analysis" ], "coreResponsibilities" : "Manage complex trial cases, Conduct legal research, Draft pleadings and motions, Manage discovery, Prepare for and take depositions, Prepare witnesses for testimony, Argue motions, Conduct trials, Negotiate settlements, Counsel clients, Handle appeals, Participate in arbitration, Participate in mediation", "teamCollaboration" : "Law firm teams; Clients", "projectManagementSkills" : [ "Case management" ], "domainKnowledge" : "Complex commercial litigation; Construction defect litigation; Employment litigation; Premises liability litigation; Product liability litigation; Catastrophic injury litigation; Medical malpractice litigation; Trucking litigation; Toxic tort litigation; Professional liability litigation; Business litigation; Appeals; Arbitration; Mediation", "domainList" : [ "complex-commercial-litigation", "construction-defect-litigation", "employment-litigation", "premises-liability-litigation", "product-liability-litigation", "catastrophic-injury-litigation", "medical-malpractice-litigation", "trucking-litigation", "toxic-tort-litigation", "professional-liability-litigation", "business-litigation", "appeals", "arbitration", "mediation" ], "domainSpecificKnowledge" : [ "Complex commercial litigation", "Construction defect litigation", "Employment litigation", "Premises liability litigation", "Product liability litigation", "Catastrophic injury litigation", "Medical malpractice litigation", "Trucking litigation", "Toxic tort litigation", "Professional liability litigation", "Business litigation", "Appeals", "Arbitration", "Mediation" ], "toolProficiency" : [ "Westlaw", "LexisNexis" ], "communicationSkills" : "Client counseling; Courtroom advocacy", "documentationSkills" : "Pleading drafting; Motion drafting; Discovery documents", "problemSolvingSkills" : "Legal analysis; Case strategy", "outcomesObjectives" : "Achieve favorable case outcomes; Successfully resolve client matters", "qualificationsBasic" : "5+ years of complex trial experience, Admission to the State Bar", "qualificationsPreferred" : "Experience with complex commercial litigation, Experience with construction defect litigation, Experience with employment litigation, Experience with premises liability litigation, Experience with product liability litigation, Experience with catastrophic injury litigation, Experience with medical malpractice litigation, Experience with trucking litigation, Experience with toxic tort litigation, Experience with professional liability litigation, Experience with business litigation, Experience with appeals, Experience with arbitration, Experience with mediation", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "Join Tyson & Mendes – Senior Counsel, Complex Trial Teams Where Insurance Defense Meets Innovation Please note: An active bar license in the State of California is required. At Tyson & Mendes, we don’t just litigate—we lead. As a national force in insurance defense and trial advocacy, we’re known for our bold mission to stop Nuclear Verdicts® and our results-driven approach to high-exposure litigation. We are expanding our Complex Trial Teams and seeking accomplished Senior Counsel ready to make an impact in the courtroom and beyond. If you are an experienced trial lawyer who thrives on complex, high-stakes cases, values strategy over spectacle, and wants to be part of a team that is reshaping the future of civil defense—this is your opportunity. Why Tyson & Mendes? Lead with Impact – As Senior Counsel on our Complex Trial Team, you’ll take the reins on challenging, high-value matters with the support and trust of a firm built for trial success. Elite Training + Resources – From our Trial Academy to dedicated jury research and litigation support, we equip you with everything you need to succeed at the highest level. Stability + Momentum – Join a financially strong, nationally scaled firm with an agile, no-silos culture that prioritizes long-term success over short-term wins. Authentic Inclusion – At Tyson & Mendes, diverse perspectives and lived experiences are essential to our approach, our outcomes, and our culture. Results Matter, Not Where You Work – Office-based, hybrid, or remote—we focus on performance and outcomes, not location. Who You Are You are a trial-tested litigator with a defense-first mindset and the strategic acumen to lead complex cases from start to finish. You bring gravitas in the courtroom, confidence in depositions, and clarity in client communication. You think like a tactician, mentor with purpose, and uphold the highest standards of ethics and advocacy. With a deep understanding of high-exposure civil litigation—especially in areas like catastrophic injury, wrongful death, or construction defect—you are ready to take the next step in your leadership and litigation career. Make Your Move. Be part of something bigger—join Tyson & Mendes and help shape the future of insurance defense. Apply today. We’re ready for your best. Responsibilities Lead Complex Trials: Represent clients in high-exposure and complex insurance defense cases, including cases involving catastrophic injury, wrongful death, property damage, and professional liability. Case Strategy and Planning: Develop and execute case strategies, including risk assessment, discovery, motion practice, and trial preparation. Client Advisement: Work closely with clients, insurance carriers, and adjusters to provide clear legal advice, case assessments, and updates on case developments. Litigation Management: Oversee all stages of litigation, including pleadings, discovery, depositions, pre-trial motions, and settlement negotiations. Courtroom Representation: Serve as lead counsel in jury trials, bench trials, and mediations, presenting cases effectively and persuasively. Team Leadership and Mentorship: Supervise and mentor junior attorneys, paralegals, and support staff, ensuring high-quality work and compliance with best practices. Collaboration with Experts: Collaborate with expert witnesses, including medical, forensic, engineering, and economic experts, to strengthen case arguments. Requirements Juris Doctor (JD) from an accredited law school. Active license to practice law in the State of California and eligibility to practice in federal courts. 8+ years of experience in insurance defense litigation with a strong focus on complex trial work. Demonstrated success as lead trial counsel in multiple high-stakes cases. Strong knowledge of civil procedure, tort law, insurance law, and trial strategies. Proven ability to manage and prioritize a large, demanding caseload with limited oversight. Exceptional oral advocacy, legal writing, and negotiation skills. Strong client relationship management skills with an ability to communicate complex legal strategies effectively. Background in catastrophic injury, construction defect, or professional liability cases preferred. Experience with e-discovery tools and case management software. Membership in local or national trial lawyer associations is a plus. Compensation Package The base salary for this position ranges from $160,000-190,000 annually, depending on experience and qualifications Attorneys are eligible for an annual billable hours bonus ranging from $10,000 and then aggregating with $7,500 for every additional tier Comprehensive benefits coverage offered, including plans available at zero employee cost (average annual employer contribution for health/vision/dental/life coverage is $700-$1,700) Employees benefit from a 401(k) program that includes a 100% match on the first 3% contributed and a 50% match on the following 4-5% Employees receive a monthly technology reimbursement of $60 Student loan repayment assistance or 529 college savings plan (full-time attorneys after one year with the firm) $100-$200/month Paid parental leave at base pay Benefits Employee Assistance Program through HealthAdvocate Comprehensive in-house training and leadership development opportunities Firm Provided CLE Programs and Paid Bar License Renewal Fees Flexible vacation policy for attorneys Defined pathway to partnership Internal diversity and inclusion programs, such as the Women’s Initiative and Young Professionals Initiative Firm-wide charitable giving program Numerous social and off-site events each year to enrich your relationships with your colleagues Flexible Work Model: Remote, hybrid, or onsite options available About Tyson & Mendes Click here to learn more about the Tyson & Mendes Office! (944) The Tyson & Mendes Office - YouTube We’re one of the fastest-growing civil defense firms in the country—known for breaking the mold of the traditional law firm. Our dynamic, diverse team of trial attorneys delivers exceptional results, from landmark cases like Howell v. Hamilton Meats to numerous defense verdicts across the nation. But we don’t stop at great legal work—we invest in our people. With specialized training in our proven defense methods, clear paths to leadership, and robust professional development, we empower attorneys to grow their careers, build their personal brands, and become leaders in the field. Follow along with the firm on Twitter and LinkedIn or visit www.tysonmendes.com. Equal Opportunity Employer Notice OK, now for the legal copy (we are a law firm, after all). It is Tyson & Mendes’ policy to ensure equal employment opportunity without discrimination or harassment on the basis of race, religion, color, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, family medical history or genetic information, political affiliation, military service, or other non-merit-based factors. By the way, if you read all of this, congratulations – we can already tell your attention to detail is exceptional. NOTICE TO APPLICANTS/EMPLOYEES OF TYSON & MENDES: Please take notice that the Firm collects certain information about you. For more information on the Firm’s policies, please refer to the document provided here. No recruiters/agencies #li-remote Pay Range $160,000—$190,000 USD", "summaryDescription" : "Senior Counsel (Complex Trial) at Tyson & Mendes LLP. Skills: Complex trial, Litigation, Legal analysis. Manage complex trial cases. Conduct legal research", "postedDate" : "2026-06-14T21:48:11.727", "createdAt" : "2026-06-14T21:48:11.727", "lastUpdated" : "2026-06-16T05:50:15.234", "ingestTimestamp" : "2026-06-14T21:48:11.727", "mongoId" : "6a2c91e974d8ee00a0984529", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 160000, "salaryAnnualMax" : 190000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Complex trial", "Commercial litigation", "Construction defect", "Employment litigation", "Premises liability", "Product liability", "Catastrophic injury", "Medical malpractice", "Trucking litigation", "Toxic tort", "Professional liability", "Business litigation", "Appeals", "Arbitration", "Mediation", "Litigation", "Legal analysis", "Trial advocacy", "Legal research", "Legal writing", "Case management", "Negotiation", "Pleading drafting", "Discovery management", "Motion practice", "Client counseling", "Deposition preparation", "Witness preparation", "Complex commercial litigation", "Construction defect litigation", "Premises liability litigation", "Product liability litigation", "Catastrophic injury litigation", "Medical malpractice litigation", "Toxic tort litigation", "Professional liability litigation", "Admission to the State Bar", "Westlaw", "LexisNexis" ], "skillCount" : 39, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "_score" : 480.8201, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Legal", "llmIndustryConfidence" : 0.98 }, { "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, "_score" : 480.53696, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2d3f1074d8ee00a0b347f0", "title" : "Data Manager for Clinical Trials", "company" : "PSI CRO", "industry" : "Pharmaceuticals", "salary" : { "min" : 75000.0, "max" : 95000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Data Manager in Mississauga, Canada, adjusted for the Biotech industry and full-time employment." }, "location" : "Mississauga, ON, Canada", "locations" : [ "Mississauga", "ON", "Canada" ], "timestamp" : "2026-06-16T06:35:51.865", "fingerprint" : "cfd7cbd62c3d5a4fc465804d775363e78d15585f2522790f8f1a3777acb0cd35", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000131986259-data-manager-for-clinical-trials", "externalId" : "744000131986259", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Mississauga", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.5884727,-79.6436580" } ], "locationText" : "Mississauga, Ontario, Canada", "employmentType" : "FULL_TIME", "minimumEducation" : "College or University degree", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "professionalSkills" : [ "Clinical data management", "Medical coding" ], "hardSkillsList" : [ "Data management", "Data reconciliation", "Query management", "Data entry", "Data listings", "Patient profiles generation" ], "hardSkills" : [ { "name" : "Data management", "level" : "intermediate" }, { "name" : "Data reconciliation", "level" : "intermediate" }, { "name" : "Query management", "level" : "intermediate" }, { "name" : "Data entry", "level" : "intermediate" }, { "name" : "Data listings", "level" : "intermediate" }, { "name" : "Patient profiles generation", "level" : "intermediate" } ], "majorSkills" : "Clinical data management, Data reconciliation, Query management", "majorSkillsList" : [ "Clinical data management", "Data reconciliation", "Query management" ], "coreResponsibilities" : "Act as communication line for project teams, Maintain TMF/eTMF, Train Assistant Data Manager, Support development of study documentation, Manage user access, Review data, Reconcile eCRF/External data, Support SAE reconciliation, Manage queries, Enter and QC local lab normal ranges, Perform Study Database Lock activities, QC archival of CRFs, Perform data entry/QC, Report project status, Generate and deliver data listings/Patient profiles, Assist with Database Lock tasks", "teamCollaboration" : "Project teams", "domainKnowledge" : "Clinical data management; Medical science; Life Science", "domainList" : [ "clinical-data-management", "medical-science", "life-science" ], "domainSpecificKnowledge" : [ "Clinical data management", "Medical science", "Life Science" ], "toolProficiency" : [ "ECRF", "TMF", "ETMF" ], "communicationSkills" : "Communication line", "documentationSkills" : "Study documentation; CRF Completion Guidelines; Data Management Plan; Edit Checks Specification; User Access Management Plan; Data Validation Plan; External Data Transfer Agreements; SAE Reconciliation Guidelines; Local Lab Normal Ranges Guidelines; Coding Guidelines", "qualificationsBasic" : "College or University degree, Minimum of one year of industry experience, Experience working with clinical or medical data", "qualificationsPreferred" : "PhD preferred, Specific ML framework experience, Cloud platform certs", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,200 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them. 1. Acts as a communication line for project teams regarding clinical data management 2. Maintains TMF/eTMF 3. Trains Assistant Data Manager 4. Is involved in clinical data management activities including, but not limited to: * Supporting development of study documentation (eCRF Requirements, Edit Checks Specification, Data Management Plan, CRF Completion Guidelines, User Access Management Plan, Data Validation Plan, External Data Transfer Agreements, SAE Reconciliation Guidelines, Local Lab Normal Ranges Guidelines, Coding Guidelines where applicable) * User acceptance testing * User access management * Data review * eCRF/External data reconciliation * Medical coding (for staff with medical/Life Science background) * Supporting SAE reconciliation * Query management * Local lab normal ranges entry and QC * Study Database Lock activities * Archival of CRFs QC * Data entry/QC * Project status reporting * Data listings/Patient profiles generation and delivery * Assisting with Database Lock tasks as needed for assigned projects ## Qualifications * College or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities * A minimum of one year of industry experience, preferably working with clinical or medical data", "summaryDescription" : "Data Manager for Clinical Trials at PSI CRO. Skills: Clinical data management, Data reconciliation, Query management. Act as communication line for project teams. Maintain TMF/eTMF", "postedDate" : "2026-06-12T20:35:30.000", "createdAt" : "2026-06-14T20:28:47.999", "lastUpdated" : "2026-06-16T06:35:51.865", "ingestTimestamp" : "2026-06-14T20:28:47.999", "mongoId" : "6a2d3f1074d8ee00a0b347f0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Data management", "Data reconciliation", "Query management", "Data entry", "Data listings", "Patient profiles generation", "Clinical data management", "Medical coding", "Medical science", "Life Science", "ECRF", "TMF", "ETMF" ], "skillCount" : 13, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 475.52997, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 } ], "status" : 200, "message" : "OK", "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 58079, "totalPages" : 1162, "hasNext" : true, "hasPrevious" : false } }

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Common Questions