Clinical Research Associate, Sponsor Dedicated

IQVIA seeks an experienced Clinical Research Associate for sponsor-dedicated monitoring and site management across multiple U.S. regions. The role involves conducting site visits, managing study progress, ensuring regulatory compliance, and supporting recruitment and enrollment activities with 65-70% travel required.

Responsibilities Conduct site monitoring visits including selection, initiation, monitoring and close-out per protocol and regulatory requirements Collaborate with sites on subject recruitment planning and tracking to meet enrollment targets Administer protocol training and maintain ongoing communication with assigned study sites Evaluate site quality and adherence to regulations; escalate compliance issues as needed Track study progress including regulatory submissions, enrollment, CRF completion and data queries Requirements 2.5+ years clinical research coordination experience at site level Bachelor's degree in life sciences or nursing (U.S. equivalent or higher) Knowledge of electronic data capture systems preferred Ability to travel 65-70% nationwide Understanding of Good Clinical Practice (GCP) and ICH guidelines Compensation:

$64,000-$189,000 base