Clinical Research Associate, Sponsor Dedicated
$64k - $189kIQVIA
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
Vacancy posted 1 day ago
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