Clinical Research Associate, Sponsor Dedicated
IQVIA(1 month ago)
About this role
This role at IQVIA focuses on overseeing clinical trial sites to ensure studies are executed correctly and study data is reported according to protocols and regulatory requirements. The position works closely with research sites and internal study teams to support successful study execution and predictable enrollment progress. It is based in the same country as the job location and includes travel for on-site activities.
Required Skills
- Site Monitoring
- Clinical Research
- Good Clinical Practice
- ICH Guidelines
- Site Management
- Subject Recruitment
- Regulatory Submissions
- CRF Review
- Data Queries
- TMF Management
+5 more
Qualifications
- Bachelor's Degree
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.
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