CRA2
IQVIA(27 days ago)
About this role
A Clinical Research Associate at IQVIA supports the conduct of clinical studies by ensuring study data and documentation meet protocol, sponsor, and regulatory requirements. The role works with study sites and internal teams to maintain data integrity, regulatory compliance, and study readiness throughout the trial lifecycle.
Required Skills
- Site Monitoring
- Recruitment Planning
- Study Training
- Regulatory Compliance
- GCP
- ICH Guidelines
- CRF Completion
- Data Queries
- TMF Management
- Documentation
+5 more
Qualifications
- Bachelor's Degree in Scientific Discipline or Healthcare
- 1 Year On-site Monitoring Experience
- Equivalent Education/Experience Accepted
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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