Clinical Research Associate: Site Monitoring & Coordination
Listed on 2026-10-18
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Research/Development
Clinical Research, Research Assistant/Associate -
Healthcare
Clinical Research
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.
Step into the Clinical Research Associate:
Site Monitoring & Coordination role at IQVIA in Overland Park, KS, United States and grow with us.
We have an opening for a Clinical Research Associate:
Site Monitoring & Coordination in Overland Park, KS, United States within Bio & Pharmacology & Health.
This role, Clinical Research Associate:
Site Monitoring & Coordination at IQVIA, could be your next career step.
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