CRA I
Fortrea(2 months ago)
About this role
A Clinical Research Associate responsible for site monitoring and site management of clinical studies, ensuring compliance with company, sponsor SOPs, and regulatory guidelines. The role supports implementation of project plans and coordination with internal teams and vendors. Travel to clinical sites for monitoring, initiation, and closeout visits is an essential function of the role.
Required Skills
- Site Monitoring
- Site Management
- Clinical Trials
- Regulatory Guidelines
- Informed Consent
- CRF Review
- Data Review
- SAE Tracking
- CTMS
- Communication
+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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