Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated

Montréal, Québec

On-site

Full-time

No salary posted2 weeks ago

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Employment type: Full-time · On-site
Posted: September 22, 2026
Province: Quebec (QC)

Hiring confidence: Sparse posting · 11/100

This posting is missing most of the signals we look for, or shows patterns common to listings that are not actively being filled. Check with the employer before applying. How this is scored

Job Overview

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Vue d’ensemble du poste Effectuer des tâches de suivi et de gestion de site pour une variété de protocoles, de sites et de domaines thérapeutiques. Doit être bilingue français et anglais et situé à Montréal. Responsabilités essentielles Effectuer des visites de suivi des sites (visites de sélection, de lancement, de suivi et de clôture) conformément à la portée contractuelle des travaux et les exigences réglementaires, c’est-à-dire les directives de pratiques exemplaires cliniques (BPC) et de l…

This role is based in Quebec. IQVIA is hiring for this full-time position through Jobily, where you can check how well your resume matches the posting before you apply.

Market context

About this role in Quebec

Average salary for Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated in Quebec

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NOC code

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Typical qualifications for Canadian employers

Bilingual: French and English fluency
Located in Montreal
Knowledge of Good Clinical Practice (GCP) guidelines
Understanding of regulatory requirements
Experience with multiple therapeutic areas

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What you'll do

Perform site monitoring visits (selection, initiation, monitoring, and closure visits)
Manage site tracking and oversight tasks
Ensure compliance with contractual scope of work
Ensure adherence to regulatory requirements
Support various protocols across different therapeutic domains
Maintain documentation in accordance with GCP guidelines

What you'll need

Bilingual: French and English fluency
Located in Montreal
Knowledge of Good Clinical Practice (GCP) guidelines
Understanding of regulatory requirements
Experience with multiple therapeutic areas
Experience with multiple protocols and sites