16252 - Sr.CRA 2
IQVIA(1 month ago)
About this role
A Clinical Research Monitor at IQVIA supporting the conduct of clinical trials across multiple therapeutic areas by managing site relationships and ensuring regulatory and quality standards are met. The role contributes to study execution and data integrity within IQVIA's global clinical research services.
Required Skills
- Site Monitoring
- GCP
- ICH
- Subject Recruitment
- Protocol Training
- Regulatory Compliance
- TMF Management
- CRF Completion
- Data Queries
- Microsoft Office
+4 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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