Clinical Research Monitor: Site & Sponsor Alignment
Listed on 2026-10-13
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Research/Development
Clinical Research
IQVIA is seeking an on-site Clinical Site Monitor in Kansas to ensure sites conduct studies per protocol and regulatory guidelines. You will perform monitoring visits, train site staff, and manage documentation across TMF/ISF while tracking enrollments and data quality.
The role requires 1+ year of on-site monitoring, strong English communication, and proficiency in MS Office; collaboration with study teams is essential. Base pay varies with experience.
For the Clinical Research Monitor:
Site & Sponsor Alignment position at IQVIA, we are reviewing applications now.
We would love to welcome a new Clinical Research Monitor:
Site & Sponsor Alignment to our group in Overland Park, KS, United States.
Step into the Clinical Research Monitor:
Site & Sponsor Alignment role at IQVIA in Overland Park, KS, United States and grow with us.
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