Clinical Trials Assistant - Multi-Sponsor - Paris based
IQVIA(1 month ago)
About this role
This role provides administrative support to clinical research teams to ensure accurate and complete Trial Master File (TMF) delivery. The position works closely with Clinical Research Associates and Regulatory/Start-Up teams to support study documentation flow and project coordination. The job sits within a clinical research services organization supporting life sciences and healthcare clients.
Required Skills
- Trial Master File
- Document Control
- Clinical Documentation
- Site Compliance
- File Archiving
- Clinical Trial Supplies
- Tracking Management
- Case Report Forms
- Query Tracking
- Data Flow
+6 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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