FSP CRA II（Shanghai）
Fortrea(1 month ago)
About this role
A Clinical Monitoring role responsible for overseeing and ensuring the quality and compliance of clinical studies at research sites. The position involves site management, data verification, regulatory adherence, and collaboration with study teams, often requiring travel to study sites.
Required Skills
- GCP
- ICH Guidelines
- Monitoring
- Clinical Trials
- Regulatory Compliance
- Data Verification
- eCRF
- SAE
- Source Document Review
- Study Management
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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