Clinical Research Associate I - Ophthalmology
Fortrea(3 months ago)
About this role
Clinical Research Associate responsible for site monitoring and site management for clinical studies, ensuring adherence to protocols, regulatory requirements, and study plans. The role supports study start-up, monitoring, closeout, and coordination with sponsors, vendors, and internal teams to maintain data integrity and patient safety.
Required Skills
- Site Monitoring
- Site Management
- Regulatory Knowledge
- CRF Review
- Data Review
- Vendor Management
- Patient Safety
- CTMS
- Project Coordination
- Communication
Qualifications
- University Degree
- Nursing License
- Valid Driver's License
About Fortrea
fortrea.comFortrea, a leading CRO, advancing clinical trials through patient-focused clinical solutions that accelerate clinical development, drive trial success, and bring innovative therapies to those who need them most.
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