eTMF Specialist- CDI - H/F
Pierre Fabre Group • Boulogne-Billancourt, France
Role Description
Your mission
We are hiring a permanent eTMF Specialist in Toulouse or Boulogne to join a team of 7 people under the hierarchical and functional responsibility of the Clinical Study Coordinators Manager in the R&D Medical Care department.
The eTMF Specialist plays a vital role within the Clinical Development Platform by overseeing the electronic Trial Master File (eTMF) system to ensure regulatory compliance, quality control, and inspection readiness across global clinical trials. This position requires expertise in clinical trial documentation management, collaboration with cross-functional teams, and active participation in audits and inspections.
Your role within a pioneering company in full expansion:
The specialist manages the setup, maintenance, and closeout of eTMFs, performs regular quality control checks, monitors metrics and KPIs to ensure document completene...