FSP CRA I（Shanghai）
Fortrea(1 month ago)
About this role
A Clinical Research Associate focused on site monitoring and site management for clinical studies, ensuring adherence to company/sponsor SOPs and regulatory guidelines. The role supports project plan implementation and contributes to study conduct and oversight across study sites.
Required Skills
- Site Monitoring
- Site Management
- CRF Review
- Data Review
- SAE Tracking
- Regulatory Knowledge
- Project Coordination
- CTMS
- Microsoft Office
- Communication
Qualifications
- University Degree
- Certification In Allied Health
- Nursing License
- 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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