Experienced Clinical Research Associate Sponsor-dedicated
IQVIA(17 days ago)
About this role
This role involves performing site monitoring and management for clinical trials, ensuring studies are conducted in compliance with regulations and study protocols. The position includes communication with study sites, tracking project progress, and maintaining documentation to support study quality and regulatory adherence.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Regulatory Compliance
- Study Management
- Data Collection
- Communication
- Documentation
- Problem Solving
- Time Management
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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