FSP CRA II (Beijing)
Fortrea(29 days ago)
About this role
A Clinical Monitoring role focused on managing and overseeing clinical studies at various sites, ensuring compliance with regulatory standards, and safeguarding data integrity. The position involves site visits, monitoring data, managing study documentation, and collaborating with study teams across different locations.
Required Skills
- ICH GCP
- Monitoring
- Source Data Verification
- Regulatory Compliance
- Clinical Trials
- eCRF
- Site Management
- Data Integrity
- SOPs
- SAE Reporting
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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