Clinical Trials Assistant
IQVIA(1 month ago)
About this role
This role supports the clinical study team by performing administrative work to ensure a complete and accurate Trial Master File (TMF) and related study documentation. The position works closely with Clinical Research Associates and Regulatory/Start-Up teams to support smooth trial execution and documentation quality within timelines.
Required Skills
- Trial Master File
- Document Control
- Clinical Documentation
- Site Compliance
- Study File Review
- Clinical Trial Supplies
- Case Report Forms
- Data Tracking
- Project Coordination
- Microsoft Excel
+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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