Offer summary
Qualifications:
4-year college degree in healthcare or life sciences preferred, 4+ years relevant clinical research experience may substitute for degree, Minimum 6 years of site monitoring experience, Expertise in complex therapeutic indications monitoring, Strong knowledge of GCP/ICH guidelines.
Key responsabilities:
- Monitor investigational sites for subject safety
- Conduct pre-study, initiation, and monitoring visits
- Ensure compliance with protocols and regulations
- Communicate findings and report issues to project teams
- Manage and resolve site-related problems proactively