CRA (Taipei)
Fortrea(2 months ago)
About this role
Clinical site monitor responsible for site monitoring and site management for clinical studies, ensuring adherence to company and sponsor SOPs and regulatory guidelines. The role supports implementation of project plans, prepares monitoring reports, and helps ensure data integrity and patient protection. Travel to study sites is required and the role may act as a local project coordinator and vendor contact for assigned studies.
Required Skills
- Site Monitoring
- Site Management
- Regulatory Knowledge
- Clinical Trials
- Source Documentation
- CRF Review
- SAE Reporting
- EDC
- IVRS
- TMF
+5 more
Qualifications
- B.A./B.S. in Science or Biology
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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