IQVIA · Durham, NC
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This role involves planning and executing independent Good Clinical Practice audits across international sites to verify regulatory compliance and adherence to company procedures. The position requires assessing findings, preparing reports for stakeholders, consulting on regulatory interpretation, and overseeing corrective action closure. The ideal candidate holds a bachelor's degree, has at least five years in pharmaceutical/technical fields with three years in quality assurance audits, and is willing to travel 30–50% annually.
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