Clinical Research Associate: Site Monitoring Expert
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 perform site monitoring and management to ensure study sites conduct and report data per protocol and guidelines. You will work to recruit subjects, administer training, and track regulatory submissions with regular communication to sites.
Ideal candidates have 2+ years of on-site CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS/eTMF. Excellent English communication and organizational skills are essential.
Consider building your career as a Clinical Research Associate:
Site Monitoring Expert at IQVIA.
The following opportunity is for a Clinical Research Associate:
Site Monitoring Expert with IQVIA.
Our organisation is growing, and we are hiring a Clinical Research Associate:
Site Monitoring Expert in Northfield, MN, United States.
This opportunity is for the Clinical Research Associate:
Site Monitoring Expert role at IQVIA.
We are seeking a motivated Clinical Research Associate:
Site Monitoring Expert to join IQVIA in Northfield, MN, United States.
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