Clinical Research Monitor: Site Oversight & Data Quality
Listed on 2026-10-17
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Research/Development
Clinical Research
IQVIA is seeking a Clinical Research Associate to perform on-site monitoring and site management across studies, ensuring data quality and regulatory compliance. You will engage with sites to drive subject recruitment, deliver protocol training, and maintain open lines of communication to manage project expectations.
The role requires a minimum of 2 years of independent CRA experience, solid GCP/ICH knowledge, and proficiency with EDC, CTMS, and eTMF systems.
The following opening is for a Clinical Research Monitor:
Site Oversight & Data Quality with IQVIA.
This is an excellent position to take on the Clinical Research Monitor:
Site Oversight & Data Quality role at IQVIA.
As a Clinical Research Monitor:
Site Oversight & Data Quality, you will play an important part at IQVIA in Melbourne, FL, United States.
We invite applications for the Clinical Research Monitor:
Site Oversight & Data Quality position located in Melbourne, FL, United States.
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