Clinical Trial Manager
ICON · Paris, France
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Trial Manager role managing end-to-end operations for assigned protocols in France within a sponsor-dedicated model. Responsible for project delivery, regulatory compliance, team leadership, and stakeholder coordination across clinical trial execution.
What they're looking for
- University degree in medicine, science, or equivalent education and experience
- Demonstrated ability to drive clinical study deliverables
- Subject matter expertise in designated therapeutic area
- Prior monitoring experience preferred
- Willingness to travel approximately 30% as required
- Legal right to work in France
What you'll be doing
- Serve as primary point of contact for assigned protocols between Country Operations and clinical trial team
- Manage end-to-end project execution including feasibility, site selection, recruitment, and study closeout
- Ensure compliance with ICH/GCP, country regulations, sponsor policies, and adverse event reporting requirements
- Lead and support local study teams including protocol training and coordination across roles
- Create and execute local risk management plans and review monitoring visit reports
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.