Fortrea

1 Job

10,821 Employees

About the Company

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network.

Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

Listed Jobs

Company Name: Fortrea
Job Title: Senior Clinical Research Associate based in France
Job Description: **Job Title** Senior Clinical Research Associate **Role Summary** Lead the monitoring of interventional clinical trials, ensuring adherence to protocols, GCP, and regulatory requirements. Build and maintain robust site relationships, coordinate cross‑functional activities, and drive continuous improvement within clinical operations. **Expectations** - 3–4 years of senior CRA experience in clinical research. - Deep knowledge of ICH‑GCP guidelines and local regulatory frameworks. - Fluency in French and English; ability to travel across France. - Strong organizational and communication skills, with a focus on timely data collection and study success. **Key Responsibilities** - Conduct site initiation, monitoring, and close‑out visits. - Verify protocol compliance, data accuracy, and regulatory documentation. - Develop and sustain relationships with investigators, site staff, and CROs. - Collaborate with study teams (clinical, data management, biostatistics, regulatory) to resolve issues and ensure milestone attainment. - Identify and implement process improvement initiatives, contributing to operational excellence. **Required Skills** - Advanced understanding of GCP, ICH regulations, and national regulatory requirements. - Excellent verbal and written communication in French and English. - Proficiency in clinical trial management systems and Microsoft Office. - Ability to manage multiple studies concurrently and prioritize tasks. **Required Education & Certifications** - Bachelor’s degree in Life Sciences, Pharmacy, Biomedical, or related field (Master’s preferred). - ICH‑GCP certification (or equivalent clinical research training) is essential.