Clinical Research Associate (Canada)
IQVIA · Quebec, Canada
Clinical OperationsFull-time$74k–$171kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Clinical Research Associate to conduct site monitoring and management for clinical trials in the Kirkland, Quebec area. The role involves ensuring sites comply with study protocols, regulatory guidelines, and sponsor requirements while managing recruitment, documentation, and data integrity throughout the trial lifecycle.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline, or equivalent education and experience
- Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Proficiency with Microsoft Word, Excel, PowerPoint, and laptop/mobile devices
- Strong written and verbal English communication skills
- Organizational and problem-solving abilities with time and financial management skills
- Ability to establish effective working relationships with sites, team members, and stakeholders
What you'll be doing
- Conduct site monitoring visits including selection, initiation, ongoing monitoring, and close-out activities per regulatory requirements
- Develop and track subject recruitment plans with sites to meet enrollment projections and project timelines
- Deliver protocol training to assigned sites and maintain regular communication to manage expectations and resolve issues
- Assess quality and integrity of site practices, escalate compliance concerns, and maintain trial and investigator site files
- Track regulatory submissions, enrollments, case report form completion, and manage data queries and resolution
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.