Clinical Research Associate: Site Monitoring & Coordination
Listed on 2026-10-06
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Research/Development
Clinical Research, Research Assistant/Associate
IQVIA LLC is seeking a Clinical Monitoring professional in Overland Park, KS, to ensure sites conduct studies per protocol and regulations. You will monitor, train, and manage site activities, data quality, and regulatory submissions, with strong communication to sponsor teams.
The role requires 1+ year of on-site monitoring, GCP/ICH knowledge, and proficiency in Word/Excel/PowerPoint. Collaboration with study teams and effective time/financial management are essential.
We invite applications for the Clinical Research Associate:
Site Monitoring & Coordination position located in Overland Park, KS, United States.
We appreciate your interest in this position.
Join IQVIA LLC and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Clinical Research Associate:
Site Monitoring & Coordination role at IQVIA LLC, based in Overland Park, KS, United States.
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