Clinical Research Associate: Site Monitor & Study Oversight
Listed on 2026-10-06
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist
IQVIA is seeking a site monitoring professional to ensure study sites conduct the protocol as required and report data accurately. You will monitor visits, manage subject recruitment plans, and maintain regulatory filings, while collaborating with study teams to support project execution.
The role requires on-site monitoring experience, strong knowledge of GCP/ICH, and excellent communication skills in English, with proficiency in MS Office tools and familiarity with TMF/ISF processes.
We are looking to fill the Clinical Research Associate:
Site Monitor & Study Oversight position at IQVIA Argentina in Overland Park, KS, United States.
This posting is for the Clinical Research Associate:
Site Monitor & Study Oversight role at IQVIA Argentina, based in Overland Park, KS, United States.
The Clinical Research Associate:
Site Monitor & Study Oversight role at IQVIA Argentina is now open for applications in Overland Park, KS, United States.
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