Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated
IQVIA · Quebec, Canada +1 more
Clinical OperationsFull-time$72k–$160kCompany career page
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Role summary
Senior Clinical Research Associate position at IQVIA responsible for site monitoring and management across multiple protocols and therapeutic areas. Requires bilingual French-English proficiency and Montreal-based location, with oversight of regulatory compliance, recruitment tracking, and site team mentoring.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline
- Minimum 3 years of site monitoring experience
- Deep knowledge of GCP and ICH regulatory guidelines
- Strong computer skills including Microsoft Office suite
- Fluent in French and English, both written and verbal
- Excellent organizational and problem-solving abilities
What you'll be doing
- Conduct site monitoring visits including selection, initiation, ongoing, and close-out activities
- Collaborate with sites to develop and track subject recruitment plans aligned with project goals
- Deliver protocol training and maintain regular communication to manage project expectations
- Evaluate site compliance with regulatory requirements and escalate quality issues
- Generate visit reports, follow-up documentation, and maintain trial and investigator files
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.