Clinical Research Associate Jobs at Fortrea Paris
Looking to advance your career as a clinical research associate in an international research environment? This role at Fortrea offers an exciting pathway into high-impact clinical research jobs, supporting global clinical trials from Paris. Ideal for professionals and those seeking a strong jobs opportunity for life science graduates, this position places you at the centre of innovation, compliance, and patient-focused research excellence.
About the Company
Fortrea is a leading global contract research organization (CRO) dedicated to advancing clinical development through scientific rigor, innovation, and patient-centric solutions. With a strong international presence, Fortrea careers offer professionals exposure to complex global trials, modern clinical technologies, and long-term growth across the life sciences sector.
Job Details:
- Job Title: Clinical Research Associate II – FSO
- Location: Paris
- Employment Type: Full-time
- Posted: Yesterday
- Job Requisition ID: 26446
About the Clinical Research Associate Role
As a Clinical Research Associate II (CRA II), you will serve as the vital connection between science and real-world clinical outcomes. In this role, you will help translate complex clinical protocols into high-quality execution at investigational sites, directly contributing to the success of global clinical trials and the delivery of innovative therapies to patients worldwide.
Key Responsibilities
- Manage clinical trial sites in accordance with Fortrea SOPs, ICH-GCP guidelines, project plans, and sponsor requirements
- Conduct all phases of site monitoring visits, including pre-study, initiation, routine, and close-out
- Ensure subject safety, protocol compliance, and data integrity throughout the study lifecycle
- Perform source data verification (SDV), query resolution, and eCRF review to maintain audit-ready data
- Maintain essential documents within eTMF and sponsor systems
- Monitor investigational product (IP) accountability, storage, and compliance with protocol and regulatory standards
- Collaborate with cross-functional teams to support site performance, timelines, quality metrics, and study goals
Required Qualifications about Clinical Research Associate
- University or college degree in life sciences, or a related allied health profession (or equivalent relevant experience)
- Strong knowledge of ICH-GCP guidelines and applicable local regulatory requirements
- Working understanding of clinical trial processes and site monitoring procedures
- High attention to detail with the ability to follow complex protocols and documentation standards
- Fluency in English (written and spoken)
- Proficiency with clinical trial systems and tools
- Ability to work independently and travel as required
Why Join a Clinical Research Associate Job at Fortrea?
- Contribute to advancing innovative therapies and improving patient outcomes through global clinical research
- Work in a collaborative environment that supports mentorship, learning, and professional growth
- Utilize modern clinical technologies and efficient systems that promote quality and compliance
- Benefit from a flexible work model, competitive compensation, and a strong focus on employee well-being.
