CRA2
IQVIA(28 days ago)
About this role
A Clinical Research Site Monitor at IQVIA oversees site performance to ensure clinical studies are conducted and reported according to the study protocol, sponsor requirements, and applicable regulations. The role supports data integrity and regulatory compliance across study sites and liaises with study teams and site staff. The position typically involves field-based work and collaboration with cross-functional project teams.
Required Skills
- Site Monitoring
- Regulatory Compliance
- Patient Recruitment
- Protocol Training
- Clinical Documentation
- TMF Management
- CRF Management
- Data Queries
- Communication
- Time Management
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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