Clinical Research Associate: Site Monitor & Trial Oversight
Listed on 2026-10-17
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist
IQVIA is seeking a Clinical Research Associate to monitor sites and ensure data quality in line with GCP/ICH guidelines across US sites.
Core duties include site monitoring visits, initiation and close-out activities, tracking regulatory submissions and enrollment, and maintaining TMF/E clinical trial documentation. The role requires 2+ years of on-site CRA experience, strong analytical skills, and effective collaboration with sponsor teams.
For the Clinical Research Associate:
Site Monitor & Trial Oversight position at IQVIA, we are reviewing applications now.
Join us at IQVIA as our next Clinical Research Associate:
Site Monitor & Trial Oversight in Lancaster, CA, United States.
We are currently recruiting a Clinical Research Associate:
Site Monitor & Trial Oversight for our team in Lancaster, CA, United States.
This is a genuine opportunity to take on the Clinical Research Associate:
Site Monitor & Trial Oversight role at IQVIA.
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