CRA2 (Freelancer)
IQVIA(3 years ago)
About this role
A Site Monitor at IQVIA supports clinical trial execution by overseeing site compliance with study protocols, sponsor expectations, and applicable regulations. The role focuses on maintaining study quality and data integrity through engagement with participating sites and coordination with study teams.
Required Skills
- Site Monitoring
- Site Management
- Subject Recruitment
- Protocol Training
- Regulatory Compliance
- GCP
- CRF Management
- TMF Management
- 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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