CRA2
IQVIA(27 days ago)
About this role
A Clinical Research Site Monitor at IQVIA supports clinical trials by ensuring investigational sites conduct studies in compliance with protocol, regulations, and sponsor requirements. The role focuses on maintaining data integrity and site readiness while serving as a point of contact between sites and the study team. It contributes to the successful execution and reporting of clinical research to advance medical product development.
Required Skills
- Site Monitoring
- GCP
- ICH Guidelines
- Regulatory Compliance
- Protocol Knowledge
- Recruitment Planning
- TMF Management
- CRF Review
- Documentation
- Communication
+3 more
Qualifications
- Bachelor's Degree in Scientific Discipline or Health Care
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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