Clinical Research Associate - Site Monitoring Specialist

IQVIA is seeking a Clinical Research Associate to monitor study sites across the United States, ensuring protocol compliance and data integrity. The role involves site visits, training, and collaboration with study teams to drive timely recruitment and quality data.

Applicants should have a CRA background with 2+ years independent on-site monitoring, strong regulatory knowledge, and proficiency in EDC/CTMS/eTMF systems. This is an on-site position requiring location within the U.S.