Senior Clinical Research Associate I - Fso

Fortrea is recruiting! ### Our FSO department in Paris is looking for a Senior Clinical Research Associate I (SCRA I). ### **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 * ### 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](https://careers.fortrea.com/us/en/eeo-and-accommodations).