CTA-Shanghai
IQVIA(1 month ago)
About this role
This role supports clinical research project teams by coordinating and maintaining key study documentation to ensure accurate Trial Master File delivery. The position works closely with Clinical Research Associates and Regulatory/Start-Up teams to keep study records complete and organized across the trial lifecycle.
Required Skills
- Trial Master File (TMF)
- Document Control
- Clinical Documentation
- Site Compliance Tracking
- Clinical Trial Supplies
- Case Report Forms (CRFs)
- Query Tracking
- Data Flow Coordination
- Project Communications
- File Archiving
+7 more
Qualifications
- High School Diploma
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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