FSP CRA I/II(Nanjing/Hangzhou)
Fortrea(2 months ago)
About this role
A Clinical Research Associate who supports clinical studies by overseeing site-level conduct and ensuring adherence to company/sponsor SOPs and regulatory requirements. The role collaborates with sponsors, vendors, and cross-functional teams to support implementation of project plans and may require travel to clinical sites.
Required Skills
- Site Monitoring
- Site Management
- Regulatory Knowledge
- Patient Safety
- Source Verification
- Data Review
- CRF Review
- SAE Reporting
- CTMS
- Vendor Management
+2 more
Qualifications
- University Degree
- Allied Health Certification
- 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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