Clinical Research Associate Sponsor-dedicated
IQVIA(2 months ago)
About this role
This role supports the oversight of clinical trial sites to ensure studies are executed and data are reported in line with the study protocol, sponsor expectations, and applicable regulations. The position works closely with investigative sites and internal study teams to maintain consistent communication and ensure study progress across assigned sites.
Required Skills
- Site Monitoring
- Clinical Trials
- GCP
- ICH
- Site Management
- Subject Recruitment
- Study Training
- Regulatory Submissions
- CRF Review
- Data Queries
+5 more
Qualifications
- High School Diploma
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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