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Job description
Centessa Pharmaceuticals is seeking an Associate Director, Clinical Quality Assurance to oversee GCP QA for Centessa-sponsored trials across Early to Late Phase, ensuring compliance with global regulations and ICH guidelines. The role leads daily clinical quality operations and maintains robust QA programs and documentation.
This position will provide QA oversight for trial documents, monitor evolving regulations, and partner with cross-functional teams to ensure compliance and inspection
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.