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