Support clinical trials remotely with ICON using French and English fluency, clinical coordination experience, and careful study documentation. Montreal or Toronto applicants are welcome.
This Clinical Associate role contributes to planning, execution, and monitoring across clinical studies. You will coordinate sites, recruitment, data collection, and monitoring visits while collaborating with Clinical Operations, Data Management, and Biometrics. The role supports accurate, compliant trial delivery.
Key Responsibilities: Assist clinical trial planning, execution, and monitoring activities
Coordinate site initiation, recruitment, data collection, and monitoring visits
Collaborate with clinical operations, data management, and biometrics teams
Maintain study documentation and records under applicable requirements
Support data cleaning,



analysis, and clinical study reports
Requirements: Full professional fluency in written and spoken French and English
Bachelor’s degree in science or healthcare-related discipline
Clinical research or healthcare experience, preferably in pharmaceutical, biotechnology, or CRO settings
Robust organization, prioritization, time management, and problem-solving skills
Willingness to travel approximately 60 percent as required
Bring bilingual communication, clinical coordination, and data accuracy skills to ICON’s clinical research activities in Montreal or Toronto.

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📌 Bilingual Clinical Research Associate (New Brunswick)
🏢 ICON Clinical Research
📍 New Brunswick