Manager d'Etudes Cliniques – CDD

• Acting as Project Manager for your studies, coordinating and supervising internal teams and external vendors (CROs)
• Overseeing study feasibility and budget estimates prepared by CROs
• Contributing to protocol in close collaboration with the Medical writer
• Leading the Clinical Trial Team for your assigned studies
• Ensuring studies are optimised and controlled in terms of cost, timelines, quality, and risk management
• Reporting study progress and budget status to project and clinical operations management

Requirements

• Postgraduate scientific degree (Master's level or equivalent) in medicine, pharmacy, or another scientific discipline
• At least 5 years’ experience managing international clinical trials
• Experience in oncology would be 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

Core Competencies

Demonstrates expertise in managing international clinical trials, with a strong focus on budget oversight, risk management, and collaboration with CROs. Proficient in protocol development and ensuring compliance with clinical regulatory standards.

Highest-signal resume keywords

• Project Management
• Clinical Trial Management
• Collaboration With CROs
• Regulatory Compliance
• Oncology Experience

Hard Skills

• Clinical Trial Management
• Budget Management
• Protocol Development
• Risk Management
• Study Feasibility Assessment

Soft Skills

• Leadership
• Communication
• Collaboration

Industry Keywords

• Clinical Trials
• Oncology
• CROs
• Regulatory Environment
• Quality Standards