Offer summary
Qualifications:
4 year college degree in healthcare or life sciences, or 2+ years clinical research experience., Minimum 3 years in on-site monitoring of clinical studies., Strong knowledge of GCP/ICH guidelines., Proficient computer and documentation skills., Valid driver’s license and passport required..
Key responsabilities:
- Monitor investigational sites for compliance and subject safety.
- Communicate with investigators and project management teams.
- Schedule and conduct site visits as per Monitoring Plans.
- Ensure completeness of essential regulatory documentation.
- Handle adverse event reporting and data verification.