Fortrea in Paris is looking for a Senior Clinical Research Associate I (SCRA I) to be Sponsor-Dedicated.

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!