RBW is supporting a small biotech to hire an experienced GCP Site Auditor on a contract basis. In this role, you will be responsible for conducting 100% audits of clinical trial sites to ensure full compliance with GCP, regulatory standards, and trial protocols. This is not a sample audit role — you will review all documentation, processes, and trial data to maintain the highest quality standards across their clinical sites.
Responsibilities:
- Perform 100% audits of clinical trial sites to ensure full compliance with GCP and regulatory requirements.
- Review all trial documentation, patient records, informed consent forms, and data.
- Conduct root cause analysis, provide feedback, and ensure corrective actions are implemented.
- Collaborate with cross-functional teams to maintain audit readiness and regulatory compliance.
Qualifications:
- Strong GCP knowledge and prior experience in clinical site auditing.
- Attention to detail with the ability to audit complex data and processes.
- Excellent communication and reporting skills.
