Senior CRA II
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Key Responsibilities
• Monitor Clinical Trials
- conduct site visits to ensure compliance with protocols, regulatory requirements and Good Clinical Practice (GCP)
- National on sites visits in France (40%).
• Site Management
- Serve as the primary point of contact for investigational sites, ensuring smooth study operations.
• Source Document Verification (SDV)
- Review and verify accuracy of clinical data collected from study sites.
• Investigator Training and Support
- Provide ongoing training to site staff on study protocols and regulatory requirements
• Reporting and Documentation
- Prepare monitoring reports, maintain study records, and contribute to overall trial documentation.
Qualifications:
• Life Sciences University degree or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
• Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.
• Thorough knowledge of monitoring procedures and basic understanding of the clinical trial process.
• Fluency in English, written and verbal.
What We Offer
• Office based or remote position
• Career growth environment in a supportive environment
• Dedicated Line Manager
• Works directly with a leading sponsor on innovative studies
• Attractive salary and Fortrea benefits If you are passionate about clinical research, thrive in a collaborative environment, and seek exciting career growth, we want to hear from you Learn more about our EEO & Accommodations request here.
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