Job Details
Are you a detail-oriented QA professional with a deep understanding of Good Clinical Practice (GCP) guidelines? If so, I want to hear from you! We are partnered with a breaking clinical biotech company seeking a highly motivated Senior QA Consultant to join their growing team.
What you'll do:
- Conduct comprehensive reviews of clinical trial protocols, informed consent documents, and other study documents to ensure compliance with GCP guidelines and regulatory requirements.
- Develop and implement effective quality management plans for clinical trials.
- Partner with sponsors, investigators, and clinical research associates (CRAs) to provide GCP expertise and guidance.
- Conduct audits of clinical trial sites to identify potential risks and ensure adherence to GCP procedures.
- Prepare comprehensive audit reports with detailed findings and recommendations for improvement.
- Stay up-to-date on the latest GCP regulations and industry best practices.
- Contribute to the continuous improvement of the company's GCP compliance program.
Apply directly or send an up-to-date resume to 'james.bayliss@rbwconsulting'