FSP CRAI (Taiyuan)
Fortrea(21 days ago)
About this role
This role involves site monitoring and management responsibilities for clinical studies, ensuring regulatory compliance, data integrity, and efficient conduct of trials. It includes liaising with vendors, overseeing site activities, and supporting regulatory and safety processes.
Required Skills
- GCP
- CRF
- Regulatory
- Data Review
- Clinical Trials
- Site Management
- Monitoring
- SAE
- QC
- CTMS
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
CRAI
Clinical Careers Page(1 month ago)
Site Monitor II - FSP
Parexel(10 months ago)
In-house CRA I/ In-house CRA II
Precision for Medicine(6 days ago)
Senior Clinical Research Associate - FSP
Parexel(13 days ago)
CRA II - Sponsor Dedicated - Madrid/Barcelona, Spain
Clinical Careers Page(6 days ago)
Clinical Research Associate/Senior Clinical Research Associate- FSP
Parexel(1 month ago)