Clinical Research Associate: Site Monitoring & Compliance
Listed on 2026-10-06
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
IQVIA is seeking a site-monitoring professional to ensure study sites follow the protocol and regulatory requirements. You will conduct monitoring visits and train site staff, while tracking recruitment and data quality across multiple studies.
The role requires at least 2 years of on-site monitoring experience, strong GCP/ICH knowledge, and excellent English communication. US residency in Wyoming/Cheyenne is expected; IQVIA offers comprehensive clinical research services globally.
Step into the Clinical Research Associate:
Site Monitoring & Compliance role at IQVIA in Cheyenne, WY, United States and grow with us.
This opportunity is for the Clinical Research Associate:
Site Monitoring & Compliance role at IQVIA.
We are seeking a motivated Clinical Research Associate:
Site Monitoring & Compliance to join IQVIA in Cheyenne, WY, United States.
Consider building your career as a Clinical Research Associate:
Site Monitoring & Compliance at IQVIA.
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