Clinical Research Monitoring Specialist
Listed on 2026-10-06
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Research/Development
Clinical Research
IQVIA is seeking a field-based clinical monitoring professional to ensure sites conduct studies per protocol, regulations, and sponsor requirements. You will monitor visits, manage data quality, and maintain essential trial documentation in collaboration with the study team.
Responsibilities include initiating monitoring visits, tracking enrollment, and ensuring accuracy of CRFs, queries, and TMF/ISF records while maintaining strong site relationships.
This role, Clinical Research Monitoring Specialist at IQVIA, could be your next opportunity.
Learn more about the Clinical Research Monitoring Specialist role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
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This posting is for the Clinical Research Monitoring Specialist role at IQVIA, based in Overland Park, KS, United States.
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