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IQVIA is seeking a QA Auditor to independently lead the full audit lifecycle for Investigator Site Audits across a diverse portfolio of clinical research programs. The role requires coordinating with global teams, evaluating findings, and preparing CAPA plans while ensuring adherence to GCP and regulatory requirements. The position involves travel 30–50% mainly in Europe, with a strong emphasis on quality compliance and continuous improvement within a global quality organization. #J-18808-Ljbffr
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