Sr.CRA1
IQVIA(4 years ago)
About this role
A Clinical Research Associate (CRA) at IQVIA supports the conduct of clinical trials by ensuring study sites operate in compliance with protocol and regulatory standards, contributing to overall data quality and trial integrity. The role involves on-site engagement with investigators and coordination with study teams to support successful study execution and reporting.
Required Skills
- Site Monitoring
- GCP
- Regulatory Compliance
- Protocol Knowledge
- Recruitment Planning
- CRF Completion
- TMF Management
- ISF Maintenance
- Data Queries
- Visit Reporting
+6 more
Qualifications
- Bachelor's Degree
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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