About this role
Fortrea is recruiting!
Our FSP department in Paris is looking for a Senior Clinical Research Associate II (SCRA II).
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.