Coordinating CRA
IQVIA(17 days ago)
About this role
A Clinical Monitor manages site visits and oversight for clinical trials, ensuring compliance with regulatory standards and protocol adherence. The role involves communication with study sites, documentation, and collaboration with research teams to facilitate study progress.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Regulatory Compliance
- Study Management
- Data Management
- Protocol Knowledge
- Communication Skills
- Documentation
- Clinical Trials
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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