Offer summary
Qualifications:
4 year college degree in healthcare or life sciences, 2+ years clinical research experience for non-degree holders, Minimum 3 years on-site monitoring experience, Knowledge of GCP/ICH guidelines, Strong written and verbal communication skills.
Key responsabilities:
- Monitor investigational sites for subject safety
- Support Project Team and Clinical Operations Team
- Verify site compliance with regulatory requirements
- Conduct various monitoring visits and audits
- Motivate sites to achieve study goals