Offer summary
Qualifications:
Minimum 2 years in clinical research, Experience as Study Nurse/Coordinator, Completed degree in natural sciences, Knowledge of ICH-GCP Guidelines, Familiar with ophthalmology clinical studies.Key responsabilities:
- Oversee daily functions of clinical trials
- Coordinate between staff, patients, and sponsors
- Maintain adherence to FDA GCP/ICH guidelines
- Manage subject study data accurately
- Complete case report forms timely