- Remote, United States
- Remote
- 5+ years
Responsible for quality assurance in clinical research, ensuring compliance with GCP and regulatory standards.
Compensation
Package includes competitive rate and benefit options
Responsibilities
- Develop and maintain monitoring SOPs and quality management documents
- Review monitoring reports, essential documents and regulatory files
- Track and verify CAPA and effectiveness of corrective actions
- Conduct or support internal audits and inspection readiness activities
- Deliver GCP and protocol training for clinical research staff
Requirements
- Bachelor's degree in a life science or related field
- Nice to have: QA certification (e.g., CQA, RQAP-GCP)