CRA II
ICON · Paris, France
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Research Associate II position supporting late-phase clinical trials across multiple therapeutic areas in France. Responsible for independent monitoring of Phase III and IV studies, ensuring protocol compliance, data quality, and regulatory adherence at investigative sites.
What they're looking for
- Advanced degree in life sciences, nursing, medicine, or related field
- Prior experience as Clinical Research Associate in CRO or pharmaceutical setting
- Demonstrated ability to manage multiple sites and studies simultaneously
- Expertise in monitoring practices, data integrity, and site management
- Fluency in French and professional English proficiency
- Strong organizational, communication, and stakeholder management skills
What you'll be doing
- Independently monitor Phase III and IV clinical trials for ICH-GCP and regulatory compliance
- Conduct site qualification, initiation, monitoring, and closeout visits across France
- Manage studies in oncology, neurology, psychiatry, obesity, cardiology, and dermatology
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Perform data review, query resolution, and collaboration with investigators and site staff
Privacy & handoff
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