FSP CRA (Xi'an)
Fortrea(21 days ago)
About this role
A Clinical Research Associate manages the oversight of clinical studies, ensuring compliance with regulatory standards and safeguarding data integrity. They coordinate with study sites, monitor progress, and assist in study administration, all while working within a regulated environment.
Required Skills
- GCP
- CRA
- Clinical Monitoring
- Regulatory Compliance
- Source Documentation
- eCRF
- SAE
- Data Verification
- Trial Management
- Regulatory Documents
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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