Clinical Research Associate - Sponsor Dedicated
IQVIA(1 month ago)
About this role
This role focuses on ensuring clinical trial sites conduct studies and report data in line with the protocol, regulatory requirements, and sponsor expectations. The position works closely with investigative sites to support study execution, communication, and documentation throughout the trial lifecycle.
Required Skills
- Clinical Monitoring
- Site Management
- GCP
- ICH
- Study Start-Up
- Site Initiation
- Close-Out Visits
- Subject Recruitment
- Protocol Training
- Regulatory Submissions
+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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