Senior GCP Audit & Quality Compliance Lead (Global)

MMS is a data-focused CRO seeking a Quality Auditor with strong GCP expertise to independently plan, conduct, and document audits across clinical trial sites and vendors. You will develop CAPA plans and ensure compliance with 21 CFR Part 11, FDA, and GxP requirements, while traveling up to 30% within the UK/EU.

The role requires a college degree or equivalent experience, excellent communication, and a proactive approach to problem solving in a regulated environment.

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