Senior CRA
ICON · Paris, France
Clinical OperationsFull-timeCompany career page
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Role summary
Senior Clinical Research Associate position at ICON overseeing clinical trial activities in a sponsor-dedicated model. Responsible for site monitoring, protocol adherence, regulatory compliance, and guidance to junior staff and site personnel across multiple concurrent trials.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Extensive Clinical Research Associate experience with strong clinical trial process knowledge
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and site management
- Proficiency with clinical trial software and relevant tools
- Strong communication and stakeholder management capabilities
- Willingness to travel approximately 60% as required
What you'll be doing
- Monitor clinical trial sites for adherence to protocols, regulatory requirements, and GCP standards
- Conduct site visits to assess performance, resolve issues, and provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train and mentor site staff and other CRAs on clinical trial conduct standards
- Build and maintain relationships with site personnel to ensure smooth trial operations
Privacy & handoff
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