Description
Fortrea's FSP department in Paris is recruiting a Senior Clinical Research Associate II (SCRA II).
Key Responsibilities:
- Monitor clinical trials by conducting site visits to ensure compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP), with 40% of site visits in France.
- Manage sites by serving as the primary point of contact for investigational sites, ensuring smooth study operations.
- Perform Source Document Verification (SDV) by reviewing and verifying the accuracy of clinical data collected from study sites.
- Provide investigator training and support by offering ongoing training to site staff on study protocols and regulatory requirements.
- 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 accredited institution (e.g., nursing licensure).
- Thorough understanding of ICH GCP Guidelines and local regulatory requirements.
- Knowledge of monitoring procedures and a basic understanding of the clinical trial process.
- Fluency in English, both written and verbal.
What We Offer:
- Office-based or remote position.
- Career growth opportunities in a supportive environment.
- Dedicated line manager.
- Opportunity to work directly with a leading sponsor on innovative studies.
- Attractive salary and Fortrea benefits.
If you're passionate about clinical research, enjoy collaborative environments, and seek exciting career growth, we'd love to hear from you!