Clinical Research Associate — Site Monitoring & Trial Data
Listed on 2026-10-17
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist -
Healthcare
Clinical Research
IQVIA is seeking a Clinical Research Associate to monitor trial sites in Oklahoma. You will ensure sites conduct studies per protocol and regulatory guidelines, and collaborate with teams to drive recruitment and data integrity.
With 2+ years of on-site CRA experience, you will manage regulatory submissions, CRFs, and TMF/ISF documentation while maintaining strong communication with investigators and sponsors. This full-time, on-site role offers competitive pay and benefits.
This role, Clinical Research Associate — Site Monitoring & Trial Data at IQVIA, could be your next opportunity.
All applications are reviewed carefully by our team.
The position is based in Lawton, OK, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 75..
We aim to respond to suitable candidates as soon as possible.
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