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In this role, you will support the delivery of high-quality clinical trials across innovative therapies, building strong site relationships and ensuring excellence in study execution.Working in this model offers close collaboration with the sponsor’s teams, strong study ownership, and the opportunity to contribute directly to advancing cutting-edge treatments for patients worldwide.Core responsibilities:Act as primary contact for assigned clinical trial sites, building strong, collaborative relationshipsManage site lifecycle from start-up through monitoring and close-out, ensuring delivery to timelines and quality standardsConduct on-site and remote monitoring, identifying risks and driving timely issue resolutionEnsure compliance with study protocol, ICH-GCP, and local regulatory requirementsOversee site performance including data quality, recruitment, training, and documentation completenessSupport study execution (e.g. feasibility, site activation, investigator meetings, audit readiness)Collaborate cross-functionally to implement site strategies and ensure successful trial deliveryRequired Qualifications:Bachelor’s degree in Life Sciences or equivalent experience5 years’ experience in clinical research, including site monitoring/site managementProven experience in Oncology , Ophthalmology, Gene Therapy or similar therapeutic areaStrong knowledge of ICH-GCP, regulatory requirements, and clinical trial processesSolid problem-solving and critical thinking skillsProficiency in German and in EnglishWillingness to travelJoin Fortrea and take ownership of clinical trial sites across innovative therapies, playing a critical role in delivering high-quality data and accelerating drug development.
Join Fortrea as a Senior Clinical Research Associate II within a sponsor-dedicated model, where you will work exclusively with a leading global biopharmaceutical partner.
This role offers strong autonomy, cross-functional collaboration, and exposure to cutting-edge clinical research.If you are passionate about advancing clinical research and want to grow your expertise in a sponsor-dedicated environment, we encourage you to apply and join us in making a meaningful impact on patients’Learn more about our EEO & Accommodations request here . #J-18808-Ljbffr
