CRA
Fortrea(2 months ago)
About this role
Clinical Research Associate responsible for managing and monitoring clinical study sites to ensure subject protection, data integrity, and compliance with ICH GCP and sponsor requirements. The role involves site initiation, routine monitoring, close-out visits, and maintaining regulatory and eTMF documentation while supporting study deliverables. Significant travel to study sites is required.
Required Skills
- Site Management
- Clinical Monitoring
- Source Verification
- Regulatory Compliance
- eCRF Review
- Data Verification
- Query Generation
- CTMS
- SAE Reporting
- Project Planning
+4 more
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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