Senior / Clinical Research Associate
IQVIA(26 days ago)
About this role
A Site Monitor at IQVIA performs monitoring and site management to ensure clinical studies are conducted and study data are reported according to protocol, regulations, and sponsor requirements. The role supports site initiation, monitoring, and close-out activities while maintaining trial documentation and collaborating with study teams to support project execution.
Required Skills
- Site Monitoring
- Subject Recruitment
- Protocol Training
- Regulatory Compliance
- GCP
- ICH
- CRF Management
- TMF Management
- Documentation
- Communication
+3 more
Qualifications
- Bachelor's Degree in Scientific Discipline or Healthcare
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
Clinical Research Associate (Biopharma)
American Association of Physicists in Medicine(7 months ago)
CRA II (Multi-sponsor) - Mexico Home Based
Clinical Careers Page(19 days ago)
Clinical Research Associate II
Parexel(2 months ago)
CRA II - Sponsor dedicated - Brazil Home Based
Clinical Careers Page(3 months ago)
Single-sponsor CRA Austria
Clinical Careers Page(2 months ago)
CRA Switzerland multi-sponsor
Clinical Careers Page(1 month ago)