FSP CRA I (Beijing)
Fortrea(1 month ago)
About this role
A clinical research professional supporting site monitoring and site management for clinical studies, ensuring compliance with company and sponsor SOPs and regulatory guidelines. The role supports implementation of project plans, coordination with internal teams and vendors, and contributes to study and registry activities across clinical sites.
Required Skills
- Site Monitoring
- Site Management
- Regulatory Guidelines
- Informed Consent
- Source Review
- Data Monitoring
- SAE Reporting
- CTMS
- Microsoft Office
- Audit Readiness
+2 more
Qualifications
- University Degree
- Nursing Licensure
- 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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