Clinical Research Associate - Site Monitoring & Impactful Trials
Listed on 2026-11-04
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
IQVIA is seeking an on-site Clinical Research Associate to monitor study sites, ensure protocol compliance, and manage data and regulatory submissions. You will train sites, track recruitment, and maintain TMF/ISF documentation while collaborating with the study team.
Required qualifications include 2+ years of CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS systems. Fluency in English and excellent communication skills are essential.
We invite applications for the Clinical Research Associate
- Site Monitoring & Impactful Trials position located in Barre, VT, United States.
We have an opening for a Clinical Research Associate
- Site Monitoring & Impactful Trials in Barre, VT, United States within Bio & Pharmacology & Health.
This role, Clinical Research Associate
- Site Monitoring & Impactful Trials at IQVIA, could be your next opportunity.
Are you ready to take on the Clinical Research Associate
- Site Monitoring & Impactful Trials role at IQVIA?
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