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Job description
Vertex Pharmaceuticals LLC seeks an Associate Director, Clinical Study Quality Lead (Hybrid) to provide strategic GCP quality oversight across clinical trials and vendors. You will develop audit plans, ensure regulatory compliance, and drive inspection readiness while collaborating with cross-functional teams.
The role requires a strong background in ICH-GCP guidelines, risk management, CAPA processes, and vendor oversight, with potential line management responsibilities in the future.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.