CRA-HK
IQVIA(6 hours ago)
About this role
This role involves conducting site monitoring and management for clinical studies to ensure compliance with protocols, regulations, and sponsor requirements. The job supports study coordination, data integrity, and site communication to facilitate successful clinical trial execution.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Regulatory Compliance
- Project Management
- Data Management
- Communication Skills
- Clinical Trials
- Documentation
- Team Collaboration
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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