Hybrid Clinical Trial Admin & Documentation Specialist
Listed on 2026-10-21
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Administrative/Clerical
Data Entry -
Healthcare
IQVIA is seeking an Administrative Support professional to assist Clinical Research Associates and the RSU team in maintaining the Trial Master File and related systems. Your work will help ensure site compliance and timely project delivery by accurately updating documents and coordinating with the clinical team.
You will handle preparation, distribution, filing, and archiving of essential clinical documentation, support review of study files for completeness, and act as a central contact for
The Hybrid Clinical Trial Admin & Documentation Specialist role at IQVIA is now open for applications in Wilmington, DE, United States.
We are seeking a motivated Hybrid Clinical Trial Admin & Documentation Specialist to join IQVIA in Wilmington, DE, United States.
Consider building your career as a Hybrid Clinical Trial Admin & Documentation Specialist at IQVIA.
The Hybrid Clinical Trial Admin & Documentation Specialist position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
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