Experienced Clinical Research Associate Sponsor-dedicated
IQVIA(2 months ago)
About this role
This role focuses on monitoring and managing clinical trial sites to ensure studies are conducted and data is reported according to protocol, regulations, and sponsor requirements. It involves direct coordination with investigative sites to support trial progress and maintain compliant study documentation within required systems and files.
Required Skills
- Site Monitoring
- Clinical Trials
- GCP Compliance
- ICH Guidelines
- Site Management
- Subject Recruitment
- Regulatory Submissions
- CRF Review
- Data Queries
- TMF Management
+8 more
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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