CRA I/II (Shanghai)
Fortrea(22 days ago)
HybridFull TimeMedior$60,000 - $80,000Clinical Research
Apply NowAbout this role
This position involves monitoring and managing clinical trial sites to ensure compliance with regulatory requirements, data integrity, and study protocols. It requires coordination with study teams, site staff, and sponsors to facilitate successful clinical research operations. The role emphasizes independent work and adherence to quality and safety standards within a dynamic clinical environment.
Required Skills
- GCP
- ClinicalMonitoring
- DataReview
- RegulatoryCompliance
- SourceDocumentVerification
- TrialManagement
- eCRF
- SAEReporting
- ProjectCoordination
- MedicalDevices
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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