Offer summary
Qualifications:
Bachelor’s degree in scientific field or equivalent experience, 5 years of clinical research or QA experience, Experience conducting vendor and site audits, Thorough knowledge of Good Clinical Practice (GCP), Regulatory inspection support experience.
Key responsabilities:
- Lead clinical trials to support compliance
- Conduct internal and external audits for GCP
- Develop audit management plans and strategies
- Report findings and verify corrective actions
- Support training and regulatory inspections