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Clinical Study Supply Manager at Excelya. About the Job. Join Excelya, where . Audacity, Care, and Energy. define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.. This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.. Main Responsibilities. Ensure timely, cost-effective, and quality-compliant delivery of clinical study supplies for CHC clinical studies . Coordinate the sourcing of clinical study drug products (placebo, investigational and marketed products) in collaboration with CMOs, CHC Development Centers, and IA sites . Manage clinical supplies budget, including forecasting and invoice tracking with CMOs . Oversee CMOs to ensure effective execution of clinical supply operations in line with study requirements . Define and implement the optimal clinical supply strategy for each study and ensure clear communication to study teams . Monitor clinical supply production plans and ensure alignment with study timelines . Lead Operational Supply Meetings with CMOs to track progress, anticipate issues, and adjust supply strategies to mitigate risks . Review and contribute to study-related documentation (protocols, pharmacy manuals, monitoring and communication plans) to optimize supply usage . Ensure proper oversight of clinical supply documentation within the (e)TMF . Identify and mitigate clinical supply-related risks as part of the study risk management approach . Contribute, as needed, to broader clinical study management activities, including process improvement and coordination of external collaborations. About You. At Excelya, . taking audacious steps is encouraged. , so we're looking for individuals who are ready to grow with us and share our values.. Experience:. Minimum 4 years of experience as Clinical Study Support Manager.. . Skills:. Solid understanding of . GxP regulations. and clinical trial operations. . Education:. Master's degree in the related field.. . Languages:. Fluent in french and in english.. Company Location: France.