FSP CRA I/II(Hefei)
Fortrea(2 months ago)
About this role
A Clinical Research Associate at Fortrea supports clinical study execution by overseeing study sites and ensuring compliance with company, sponsor SOPs, and regulatory guidelines. The role works within project teams and interfaces with internal and external stakeholders. It typically involves travel for site visits and coordination of study documentation and regulatory communication.
Required Skills
- Site Monitoring
- Site Management
- CRF Review
- Source Review
- Regulatory Knowledge
- Clinical Trials
- CTMS
- SAE Tracking
- Data Review
- Audit Readiness
+2 more
Qualifications
- University Degree
- Certification In Allied Health (e.g., Nursing Licensure)
- 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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