CRA II / SR CRA
Fortrea(1 month ago)
About this role
A Clinical Research Associate at Fortrea oversees clinical study sites to ensure compliance with study protocols, regulatory requirements, and ICH GCP. The role supports study conduct through monitoring visits, data verification, and coordination with study teams and sponsors. It requires frequent travel to study sites and contributes to audit readiness and study deliverables.
Required Skills
- Site Management
- Clinical Monitoring
- ICH GCP
- Source Review
- eCRF Review
- Data Verification
- Query Resolution
- Regulatory Compliance
- SAE Reporting
- CTMS
+4 more
Qualifications
- University Degree
- Certification In Allied Health
- Nursing Licensure
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
FSP CRA II/ Snr CRA
Clinical Careers Page(1 month ago)
CRA II (Melbourne/ Sydney)
Clinical Careers Page(2 months ago)
Single Sponsor CRA I / II (Must have UK monitoring exp. Phase I exp. preferred.)
Clinical Careers Page(12 days ago)
Clinical Research Associate II-Taiyuan
Parexel(1 month ago)
CRA Nederland
Clinical Careers Page(3 months ago)
Sponsor dedicated CRA I/II - Home based ITA
Clinical Careers Page(1 month ago)