CTA (Beijing)
IQVIA(2 months ago)
About this role
This role provides administrative support to clinical research teams to ensure Trial Master File (TMF) documentation is complete, accurate, and delivered properly. It works closely with Clinical Research Associates and Regulatory/Start-Up teams to support clinical trial documentation workflows and project communications within timelines.
Required Skills
- Trial Master File
- Clinical Documentation
- Document Control
- Regulatory Compliance
- Site Compliance
- Clinical Trial Supplies
- Tracking Logs
- Case Report Forms
- Query Management
- Data Flow
+8 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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