Associé(e) de recherche clinique (ARC) principal(e) or Attaché(e) de recherche clinique II / Senior Clinical Research Associate or CRA 2

IQVIA seeks an experienced Clinical Research Associate to monitor and manage investigator sites across clinical trials in the Kirkland, Quebec area. The role involves conducting site visits, ensuring protocol compliance, managing recruitment, and maintaining regulatory documentation.

Responsibilities

• Conduct site monitoring visits including selection, initiation, routine monitoring, and closeout activities
• Develop and track subject recruitment plans with sites to improve enrollment predictability
• Deliver protocol training and maintain regular communication to resolve project issues
• Assess site quality and protocol compliance; escalate regulatory concerns as needed
• Track study progress including regulatory submissions, enrollment, CRF completion, and data query resolution

Requirements

• Bachelor's degree in scientific or healthcare discipline
• Minimum 2 years of on-site monitoring experience in clinical research
• Strong knowledge of GCP guidelines and ICH regulatory requirements
• Proficiency with Microsoft Office, laptops, and mobile devices
• Fluent written and verbal English and French
• Strong organizational and problem-solving skills
• Ability to manage time and budgets effectively