Clinical Research Associate — On-Site Monitoring & Study Delivery
Listed on 2026-10-15
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist -
Healthcare
Clinical Research
IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure compliant data reporting in line with the protocol and regulations. The role requires coordinating site visits, training, and documentation to support study progress in the US.
The candidate will track regulatory submissions, recruitment, CRF completion, and data queries, while maintaining TMF/ISF records and collaborating with the study team.
We invite applications for the Clinical Research Associate — On-Site Monitoring & Study Delivery position located in Lawton, OK, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Research Associate — On-Site Monitoring & Study Delivery role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
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