Coordinateur(rice) de projets cliniques - CDD H/F
Core
Clinical project coordinator supporting managers in setting up, coordinating, and executing real-world clinical studies to ensure quality, cost, and timeline compliance.
Role type
Clinical Project Coordinator (Real-World Evidence)
Builds
Real-world clinical studies (interventional and non-interventional)
Domain
Pharmaceutical / Dermo-cosmetics / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical study coordination, Trial Master File (TMF/eTMF) management, contract tracking with centers and experts, budget monitoring, CRO management, GCP/regulatory knowledge, data quality stewardship, project planning and stakeholder follow-up
Preferred skills
ARC certification, experience in pharmaceutical labs or CROs, RWE study experience, advanced Excel and Veeva eTMF proficiency
Technologies
Veeva eTMF, Excel
Responsibilities
Assist in study document management, track contracts with centers and experts, contribute to study tracking dashboards, monitor study budgets, support planning and stakeholder follow-up, organize key study meetings, manage TMF quality and archiving, supervise project contributors and CROs, ensure data quality in internal tracking tools, communicate study progress to PMO director, manage team training and handovers
Seniority
Mid-level, hands-on IC