Clinical Trial Assistant, HYBRID in Wilmington, DE

IQVIA • Wilmington, NC, US • published 2026-09-19 05:37:23.280870

Description

Wilmington, United States of America \| Full time \| Hybrid \| R1569476 Essential Functions * Assist Clinical Research Associates (CRAs) and Regulatory and Start\-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. * Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. * Assist with periodic review of study files for completeness. * Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. * Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. * Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. * May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training. Qualifications * Bachelor's Degree Required * 3 years administrative support experience. * Equivalent ...

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