Act as Project Manager for assigned studies, coordinating and supervising internal teams and external vendors (CROs) using appropriate project management and performance monitoring tools
Oversee study feasibility assessments and budget estimates prepared by CROs
Define and prepare all performance indicators and oversight tools used to monitor vendors' activities
Contribute to the protocol in close collaboration with the Medical Writer and develop study documents
Lead the Clinical Trial Team for assigned studies
Ensure studies are optimized and controlled in terms of cost, timelines, quality, and risk management
Ensure full compliance with Good Clinical Practice, internal procedures, and Pierre Fabre ethical standards
Supervise study administrative and document management activities performed by Clinical Study Coordinators
Report study progress and budget status to project and clinical operations management
Act as a mentor and point of reference for junior Clinical Study Managers

Postgraduate scientific degree (Master’s level or equivalent) in medicine, pharmacy, or another scientific discipline
Minimum 5 years’ experience managing international clinical trials
Experience in oncology is an asset
Proven track record of successful collaborations with international CROs on strategic, project-based studies
Strong understanding of the clinical regulatory and quality environment
Fluent in English, both spoken and written

Clinical Study Manager – Permanent

Key skills