Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated
IQVIA · Ontario, Canada
Clinical OperationsFull-time$103k–$153kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a bilingual senior clinical research associate to oversee site monitoring and management across multiple protocols and therapeutic areas in Montreal. The role involves conducting regulatory site visits, managing recruitment, maintaining study documentation, and mentoring clinical staff.
What they're looking for
- Bachelor's degree in science or healthcare discipline
- Minimum 3 years of site monitoring experience
- Deep knowledge of GCP and ICH regulatory guidelines
- Fluent in French and English; located in Montreal
- Proficiency with Microsoft Office suite and mobile devices
- Strong written and verbal communication skills
- Excellent organizational and time management abilities
What you'll be doing
- Conduct site selection, initiation, monitoring, and close-out visits per regulatory requirements
- Develop and track subject recruitment plans with assigned sites to meet project timelines
- Deliver protocol training to sites and maintain regular communication on project status
- Monitor study progress including regulatory approvals, enrollment, CRF completion, and data queries
- Mentor clinical staff through co-monitoring visits and provide ongoing training
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.