Clinical QC Consultant
Medvacon Life Sciences, LLCNew Jersey, United States
Posted March 20, 2026
Full Time
About the Company
No company description available.
Job Description
The Clinical QC Consultant is responsible for ensuring the quality, accuracy, and compliance of clinical trial documentation and data. This role supports clinical operations by performing quality control reviews and ensuring adherence to regulatory requirements and internal standards.
Requirements
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
- 5+ years of experience in clinical research, QA/QC, or clinical operations
- Strong knowledge of FDA regulations, ICH guidelines, and GCP
- Experience reviewing clinical trial documentation and TMF management
- High attention to detail and strong analytical skills
Benefits
- Paid time off
- Retirement plan
- 401k matching
