Study Start-Up CRA
IQVIA(1 month ago)
About this role
The Study Start-Up CRA role focuses on setting up clinical trial sites and guiding them from initial allocation through readiness (“Green Light”) for Phase I–IV studies. The position serves as the primary point of contact for sites during selection and start-up, coordinating documentation and submissions with internal teams and external stakeholders to meet country commitments and timelines.
Required Skills
- Site Selection
- Study Start-Up
- Clinical Monitoring
- ICH-GCP
- Regulatory Submissions
- IRB-IEC
- Health Authority
- TMF Management
- Document Collection
- Site Green Light
+6 more
Qualifications
- University 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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