Experienced CRA, Sponsor Dedicated - Italy
IQVIA(9 months ago)
About this role
A Clinical Research Associate (CRA) at IQVIA supports the conduct and quality of clinical trials by ensuring sites adhere to protocol, regulations, and sponsor requirements. The role is field-based and works with study teams and investigator sites to support reliable study execution and data integrity.
Required Skills
- Site Monitoring
- Recruitment Tracking
- Protocol Training
- Regulatory Compliance
- GCP
- ICH
- CRF Management
- TMF Filing
- Documentation
- Communication
+1 more
Qualifications
- Bachelor's Degree
- Master's Degree
- CRA Certification (Ministerial Decree 15.11.2011)
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
View more jobs at IQVIA →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 IQVIA
Similar Jobs
CRA Switzerland multi-sponsor
Clinical Careers Page(1 month ago)
Single-sponsor CRA Austria
Clinical Careers Page(2 months ago)
CRA II - Sponsor dedicated - Brazil Home Based
Clinical Careers Page(3 months ago)
Sponsor dedicated CRA I/II - Home based ITA
Clinical Careers Page(2 months ago)
CRA II (Czechia) sponsor dedicated, homebased
Clinical Careers Page(1 month ago)
CRA I (Sponsor dedicated) Athens Homebase
Clinical Careers Page(29 days ago)