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Company Description
Fortrea (Nasdaq: FTRE) is a global clinical research organization (CRO) delivering innovative development solutions to the life sciences industry. With over 30 years of clinical research expertise, Fortrea supports biotech, biopharma, medical device, and diagnostic innovators with agile FSO, FSP, and hybrid solutions. The company provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services across 20+ therapeutic areas. Operating in approximately 100 countries, Fortrea combines scientific rigor and operational excellence to bring predictability to clinical trial execution. Visit to learn more.
Role Description
This is a full-time on-site role for a Clinical Research Associate located in Paris Area. The Clinical Research Associate will oversee the operational aspects of assigned clinical trials, ensuring compliance with protocols, regulatory guidelines, and company standards. Responsibilities include monitoring trial sites, performing site evaluations, maintaining study documentation, and ensuring proper conduction of clinical trials. The role involves regular collaboration with site investigators and clinical teams to achieve project goals.
Qualifications
- Deep knowledge of protocols and operational guidelines in clinical research
- Experience in working on clinical trials and clinical research operations
- Strong understanding of Clinical Research Associate responsibilities and regulatory requirements
- Ability to conduct site evaluations effectively and ensure compliance with study guidelines
- Excellent organizational, communication, and problem-solving skills
- Willingness to travel within the assigned geographic region
- Bachelor's degree in Life Sciences, Pharmacy, or a related field
- Previous experience in a similar role or environment is preferred
