FSP CRAI (Guangzhou)
Fortrea(14 days ago)
About this role
A Clinical Research Associate manages various aspects of clinical study site monitoring, including ensuring regulatory compliance, data integrity, and effective communication with study staff and vendors. The role supports the successful execution of clinical trials by maintaining site readiness and overseeing study procedures.
Required Skills
- Regulatory Guidelines
- Clinical Trials
- Site Management
- Data Review
- GCP
- CRF
- Monitoring
- Investigator Coordination
- Medical Devices
- Project Coordination
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.
View more jobs at Fortrea →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Fortrea
Similar Jobs
CRA II (Multi-sponsor) - Argentina Home Based
Clinical Careers Page(11 days ago)
Senior Clinical Research Associate - Oncology - West Coast - FSP
Parexel(19 days ago)
Senior Clinical Research Associate - FSP - Remote
Clinical Careers Page(11 days ago)
Sr CRA 1
IQVIA(2 hours ago)
CRA II/ SCRA (Sydney/ Melbourne/ Brisbane)
Clinical Careers Page(12 days ago)
CRA 2
IQVIA(1 month ago)