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Manager d'Etudes Cliniques – CDD
Pierre Fabre GroupClinical Study Manager overseeing international interventional clinical trials in oncology and dermatology. Leading project management within the Clinical Operations Team at Pierre Fabre Laboratories.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
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 ManagementClinical Trial ManagementCollaboration With CROsRegulatory ComplianceOncology Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ManagementBudget ManagementProtocol DevelopmentRisk ManagementStudy Feasibility Assessment
Soft Skills
LeadershipCommunicationCollaboration
Industry Keywords
Clinical TrialsOncologyCROsRegulatory EnvironmentQuality Standards
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Benefits
Comp & perks- Incentives
- Profit-sharing
- Pierre Fabre shareholding with matching contribution
- Health and provident insurance
- 16 days of holidays (RTT) in addition to 25 days of personal holidays
- Public transport participation