Clinical Research Associate: Site Monitoring & Data Quality
Listed on 2026-10-17
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Research/Development
Clinical Research, Research Assistant/Associate -
Healthcare
Clinical Research
IQVIA is seeking a Clinical Research Associate to perform on-site monitoring visits in accordance with GCP and protocol requirements. You will ensure site readiness, oversee data quality, and engage with sites to support recruitment and regulatory submissions.
The role requires at least 2 years of independent CRA experience, strong regulatory knowledge, and excellent communication. Proficiency with EDC/CTMS/eTMF is expected.
We would love to welcome a new Clinical Research Associate:
Site Monitoring & Data Quality to our organisation in O’Fallon, MO, United States.
All applications are reviewed carefully by our team.
The position is based in O’Fallon, MO, 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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