FSP SCRA I (Beijing)
Fortrea(26 days ago)
About this role
The Senior CRA I is responsible for site monitoring and management in clinical trials, ensuring compliance with regulations and study protocols. They oversee site activities, coordinate with vendors, and act as a project lead for specific tasks, contributing to the successful execution of clinical research projects.
Required Skills
- Clinical Monitoring
- Regulatory Compliance
- Site Management
- Study Coordination
- Data Review
- SAE Reporting
- Project Management
- Regulatory Knowledge
- Communication Skills
- Investigator Recruitment
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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