Associate Director, GCP QA – Clinical Trials

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

For the Associate Director, GCP QA – Clinical Trials position at Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, we are reviewing applications now.

We are seeking a motivated Associate Director, GCP QA – Clinical Trials to join Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company in Boston, MA, United States.

Consider building your career as a Associate Director, GCP QA – Clinical Trials at Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company.