Offer summary
Qualifications:
Bachelor's degree in life science/related field, advanced degree preferred, Minimum of 4+ years in clinical research industry, Proven track record managing clinical trials and site monitoring, In-depth knowledge of clinical trial processes, GCP, and regulatory requirements, Ability to travel for site visits.
Key responsabilities:
- Plan and conduct routine monitoring visits
- Oversee site staff execution of the study
- Review and verify source data against CRFs
- Ensure clinical trials comply with regulatory requirements
- Prepare detailed monitoring visit reports