FSP CRA II
Fortrea(6 months ago)
About this role
A Clinical Research Associate at Fortrea is responsible for supporting clinical studies by overseeing site activities to ensure compliance with protocols, regulatory requirements, and company standards. The role focuses on protecting subject safety and maintaining data integrity across study sites. It involves collaboration with study teams and travel to investigator sites as required.
Required Skills
- Site Management
- Clinical Monitoring
- ICH GCP
- Source Verification
- Regulatory Compliance
- eCRF Review
- SAE Reporting
- CTMS
- Data Integrity
- Travel Management
+1 more
Qualifications
- University Degree
- Nursing Licensure
- Allied Health Certification
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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