Clinical Research Associate - Sponsor Dedicated
IQVIA(3 months ago)
About this role
This role supports the successful execution of clinical trials by overseeing study sites and ensuring study data is reported according to protocol, regulations, and sponsor expectations. The position serves as a key point of contact for assigned sites throughout the study lifecycle, helping maintain study oversight, documentation readiness, and operational progress.
Required Skills
- Site Monitoring
- Site Management
- Clinical Trials
- Good Clinical Practice
- ICH Guidelines
- Subject Recruitment
- Regulatory Submissions
- CRF Management
- Data Queries
- TMF Filing
+8 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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