Senior Clinical Trial Associate
ICON · Paris, France
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Trial Associate role supporting the management and execution of clinical trials through administrative and operational tasks. The position involves handling documentation, regulatory submissions, site coordination, and stakeholder engagement across complex trial projects.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive clinical trial support experience with solid understanding of trial processes
- Strong organizational and multitasking abilities managing multiple concurrent projects
- Proficiency in clinical trial management systems and data management software
- Excellent communication and interpersonal skills with cross-functional teams
- Willingness to travel approximately 10% as required
- Legal right to work in France
What you'll be doing
- Own clinical trial management deliverables and apply expertise to complex operational challenges
- Manage documentation, coordinate meetings, and maintain trial-related records
- Prepare and submit regulatory documents while ensuring protocol and regulatory compliance
- Monitor trial progress, manage site communications, and coordinate timely delivery of materials
- Build and maintain relationships with site staff and stakeholders to support trial success
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.