Clinical Research Associate II
Fortrea(3 months ago)
About this role
A Clinical Research Associate at Fortrea oversees site management and monitoring of clinical studies to ensure compliance with Fortrea SOPs, ICH GCP, and applicable regulatory requirements. The role supports trial conduct from pre-study through close-out, protecting participant safety and ensuring data integrity. Frequent travel to study sites is required.
Required Skills
- Site Management
- Clinical Monitoring
- Source Verification
- Regulatory Compliance
- eCRF Review
- SAE Reporting
- CTMS
- Data Management
- Microsoft Office
- Communication
Qualifications
- University Degree
- Allied Health Certification
- 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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