FSP CRA I (Shenyang, Changchun)
Fortrea(1 month ago)
About this role
A site monitoring and site management role supporting clinical studies to ensure study conduct aligns with company, sponsor SOPs, and regulatory guidelines. The position contributes to implementation of project plans and requires coordination with internal teams, vendors, and occasional travel.
Required Skills
- Site Monitoring
- Site Management
- Informed Consent
- Source Review
- CRF Review
- SAE Tracking
- Regulatory Knowledge
- CTMS
- Audit Readiness
- Travel Coordination
+2 more
Qualifications
- University Degree
- Allied Health Certification
- 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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