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 .