Offer summary
Qualifications:
Bachelor’s degree or RN in a related field, Experience in site management and monitoring, Understanding of clinical trial management principles, Knowledge of Good Clinical Practice/ICH Guidelines, Strong computer skills and communication abilities.
Key responsabilities:
- Oversee site management, monitoring, and compliance
- Identify and mitigate risks in project management
- Coordinate with cross-functional teams for study milestones
- Conduct training and ensure understanding of protocols
- Manage client communications and status updates