Oncology- Clinical Research Associate
IQVIA(15 days ago)
About this role
This role involves monitoring and managing clinical study sites to ensure compliance with study protocols and regulations. It includes overseeing site activities, ensuring data quality, and collaborating with study teams to support trial success.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Regulatory Requirements
- Data Management
- Protocol Knowledge
- Communication Skills
- Organizational Skills
- Microsoft Office
- 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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