Clinical Research Associate II (CRA2)
Fortrea(5 months ago)
About this role
A Clinical Site Monitor at Fortrea supports clinical research operations by ensuring studies are conducted in compliance with regulatory and company standards. The role typically requires clinical monitoring experience and involves frequent travel to study locations.
Required Skills
- Site Monitoring
- Site Management
- Monitoring Procedures
- Clinical Trials
- ICH GCP
- Regulatory Requirements
- SAE Reporting
- Vendor Liaison
- Study Documentation
- Planning
+2 more
Qualifications
- University Or College Degree
- Certification In Allied Health Profession
- Nursing Licensure
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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