About this opportunity
Vertex Pharmaceuticals Incorporated lists this Clinical Study Quality Lead - Hybrid/On-Site QA (GCP) opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Vertex Pharmaceuticals Incorporated seeks a Senior Manager, Clinical Study Quality Lead to provide study-level GCP QA oversight for assigned trials and partner with clinical study teams, CROs, and investigator sites. The role focuses on risk-based audit strategy, CAPA support, and inspection readiness in a sponsor-regulated environment.
Required are aBachelor's degree and 6+ years of hands-on GCP QA experience, with strong knowledge of ICH GCP E6(R3) and global regulations.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.