Job Summary
A company is looking for a GCP Auditor/Compliance Specialist to support clinical research quality assurance efforts.
Key Responsibilities
- Perform audits of clinical trial sites to ensure adherence to Good Clinical Practice (GCP) guidelines
- Contribute to the development and maintenance of the Quality Management System (QMS)
- Oversee QA functions including training programs, document control, and CAPA processes
Required Qualifications
- Bachelor's degree required
- Demonstrated experience in clinical site GCP auditing is essential
- Understanding of regulatory audit processes and quality systems within Contract Research Organizations (CROs)
- Solid grasp of current GCP regulations
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