Clinical Trials Assistant (CTA) (Evergreen)
IQVIA(1 year ago)
About this role
A Clinical Trial Documentation Specialist at IQVIA supports clinical research operations by ensuring accurate clinical documentation and Trial Master File delivery for studies. The role serves as a central contact for project communications between clinical and regulatory teams and helps maintain compliance with applicable clinical research standards. It contributes to IQVIA’s mission of accelerating development and commercialization of medical treatments.
Required Skills
- Document Filing
- TMF Management
- CRF Tracking
- Clinical Monitoring
- Clinical Supplies
- Regulatory Knowledge
- Microsoft Word
- Microsoft Excel
- PowerPoint
- Communication
+2 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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