Lead Clinical Research Associate

il y a 2 jours


Paris, France CHEManager International Temps plein

Lead Clinical Research Associate TFS HealthScience is a leading global mid‑size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout the entire clinical development journey. Our expertise includes full‑service capabilities, resourcing, and Functional Service (FSP) solutions. About This Role As part of our Strategic Resourcing Solutions (SRS) team, you will work alongside passionate and innovative professionals to ensure our customers achieve their goals. The Lead CRA is responsible for coordinating and overseeing the country and site management activities during study conduct, following company policies, SOPs and regulatory requirements, and managing financial and contractual obligations. Key Responsibilities Support the Project Manager and oversee all aspects of monitoring and site management activities, ensuring compliance with ICH/GCP guidelines, SOPs and protocol requirements. Lead, manage and guide CRAs, providing training and quality oversight of site management activities while proactively identifying potential operational issues and ensuring study deliverables. Develop study monitor plans, monitor and site training plans, verification initiatives, coordinate study investigator meetings, and review site and country study reports. Ensure study processes, procedures and expectations align with the practical realities of conducting the trial from feasibility through to close‑out. Serve as the initial point of contact for the monitoring team and support liaison with investigative site personnel. Implement monitoring and recruitment plans and support the design of CRF completion guidelines. Qualifications Bachelor’s Degree in life sciences, nursing or equivalent. Minimum 3 years of experience as a CRA, including on‑site monitoring experience. Able to work in a fast‑paced environment with changing priorities. Strong understanding of basic medical terminology and science related to the assigned drugs and therapeutic areas. Knowledge of Good Clinical Practice regulations and ICH guidelines. Ability to work independently as well as in a matrixed team environment across multiple projects. Excellent written, verbal, and computer communication skills. Excellent organizational and line‑management skills. Willingness to travel 10–20%. What We Offer We provide a competitive compensation package, comprehensive benefits, and opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, innovation, and making a difference in the lives of patients. About Us Our journey began over 25 years ago in Lund, Sweden. As a global CRO committed to patient safety and well‑being, we offer tailored clinical development solutions. We operate in 17 countries across Europe, North America, Asia Pacific and the Middle East. Our core values of Trust, Quality, Flexibility and Passion guide our culture and work ethic. #J-18808-Ljbffr



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