Coordinate day-to-day operational and logistical activities of clinical studies
Support planning and follow-up of visits (site selection, initiation, monitoring, close-out)
Actively contribute to study meetings and track key performance indicators
Oversee study delivery at sites, ensuring quality and client satisfaction
Assist with regulatory submissions (ethics committees, ANSM — French National Agency for Medicines and Health Products Safety)
Monitor contractual workflows: single-site agreements, amendments, budget annexes
Liaise with legal, clinical, and institutional stakeholders to ensure compliance
Contribute to site budget tracking and payment follow-up in coordination with Finance
Support the development of tools, trackers, SOPs, and internal templates
Maintain regulatory documentation and ensure audit readiness
Ensure ongoing compliance with GCP, Jardé Law, ICH guidelines, and GDPR
Work closely with Clinical Scientists, Biostatistics, and Product teams
Participate in internal alignment meetings and external study governance committees
Take part in clinical operations initiatives and cross-functional projects

Degree in life sciences, pharmacy, clinical research, or biomedical engineering
2+ years of experience in clinical research (CRA, site manager, or junior project management)
Professional fluency in both French and English, written and spoken

Clinical Trial Manager

Key skills