Conduct GCP audits (e.g., site, vendor, document, system audits).
Ensure clinical trial compliance with FDA, EMA, ICH, and other regulatory bodies.
Identify quality issues and collaborate on corrective/preventive actions (CAPAs).
Support inspection readiness and regulatory agency audits.
Maintain quality documentation and QA metrics.
Job Type: Full-time
Pay: ?330,000.00 - ?650,000.00 per year
Benefits:
Health insurance
Work Location: In person
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