CRA 2 - Single Sponsor Dedicated
IQVIA(18 days ago)
About this role
IQVIA is seeking experienced Clinical Research Associates in the UK to perform site monitoring and management for clinical studies. The role involves ensuring compliance with regulations, supporting study progress, and maintaining documentation.
Required Skills
- GCP
- ICH Guidelines
- Site Management
- Regulatory Compliance
- Clinical Trials
- Data Management
- Monitoring
- Communication
- Organization
- Problem Solving
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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