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Clinical Research Associate, Sponsor Dedicated, IVD

IQVIA • Overland Park, KS, US • published 2026-11-10 12:59:10.288467

Description

Overland Park, United States of America \| Full time \| Field\-based \| R1579059 **Position Summary** The Clinical Research Associate (CRA) will be responsible for designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Responsibilities include but are not limited to: * Ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures, good clinical practices and other applicable regulatory requirements; * Validating product performance claims; * Supplying data for critical Regulatory submissions; * Defining the functional and clinical utility of investigational products, and * Obtaining opinions and input regarding investigational products from laboratories or customers, who may be considered key opinion leaders. The CRA is responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions. **Job Function/Responsibilities** * Performing or coordinating aspects of clinical studies including site selection, study initiation, site monitoring, and study closeout. * ...

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