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
Mid-level clinical project coordinator (real-world evidence)
Builds
Real-world clinical studies (interventional and non-interventional)
Domain
Pharmaceutical / Clinical Research
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 RWE studies, advanced Excel and Veeva eTMF
Technologies
Veeva eTMF, Excel
Responsibilities
Assist Project Managers in study setup and execution; manage study documents and TMF; track contracts with centers and experts; monitor study budgets and invoices; coordinate operational aspects of multicentric studies; ensure data quality and compliance with GCP; organize key study meetings and prepare presentation materials; supervise administrative and documentation management; communicate study progress to PMO; manage team training and handovers.
Seniority
Mid-level, hands-on IC
