Clinical Trials Assistant (Guangzhou)
IQVIA(2 months ago)
About this role
This role provides administrative support to clinical operations teams to ensure Trial Master File (TMF) documentation is complete, accurate, and delivered on time. It partners closely with Clinical Research Associates and Regulatory/Start-Up teams to support study documentation flow and project communications within IQVIA’s clinical research services organization.
Required Skills
- Trial Master File
- Document Management
- Clinical Documentation
- Site Compliance
- File Archiving
- Clinical Trial Supplies
- Tracking Management
- Case Report Forms
- Query Management
- Clinical 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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