FSP CRA(Guangzhou and Southern cities)
Fortrea(10 months ago)
About this role
A Clinical Research Associate (CRA) candidate for Fortrea’s future opportunities, focused on supporting clinical trial site operations and ensuring study documentation and regulatory readiness. The role aligns candidates with Fortrea’s monitoring needs across trials conducted under ICH GCP and company SOPs and involves collaboration with study teams and sponsors.
Required Skills
- Site Management
- Clinical Monitoring
- Source Verification
- Regulatory Compliance
- eCRF Review
- SAE Reporting
- Data Integrity
- CTMS
- Report Writing
- Communication
Qualifications
- University or College Degree
- Certification in Allied Health
- 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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