Global CTA
IQVIA(1 month ago)
About this role
This role provides administrative support to clinical research teams to ensure complete and accurate delivery of the Trial Master File (TMF). The position partners closely with Clinical Research Associates and Regulatory/Start-Up teams to support documentation, communications, and trial supply tracking for clinical studies at IQVIA.
Required Skills
- Trial Master File
- Clinical Documentation
- Document Control
- Site Compliance
- Study Filing
- Archiving
- Clinical Trial Supplies
- CRF Tracking
- Query Tracking
- Data Flow
+8 more
Qualifications
- Bachelor Degree in Life Science or Health Care
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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