Clinical Research Associate: Site Monitoring & Trials
Listed on 2026-10-15
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist
IQVIA is seeking a Clinical Research Associate to perform site monitoring and ensure protocol adherence across study sites. You will manage recruitment plans, training, and regular communications with sites to meet sponsor and regulatory requirements.
Requires 2+ years on-site CRA experience, knowledge of GCP/ICH, and proficiency with EDC/CTMS/eTMF; strong English communication and organizational skills are essential.
The following position is for a Clinical Research Associate:
Site Monitoring & Trials with IQVIA.
For the Clinical Research Associate:
Site Monitoring & Trials position at IQVIA, we are reviewing applications now.
Step into the Clinical Research Associate:
Site Monitoring & Trials role at IQVIA in Afton, WY, United States and grow with us.
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