Join the innovative team at Bruyère Health Research Institute as a Research Project Specialist 2. This casual role allows you to coordinate and conduct impactful clinical trials focused on brain health.

In this position, you will support the successful execution of both pharma-sponsored and investigator-initiated trials. Your duties as a registered nurse will involve patient assessments, documenting the consenting process, and overseeing clinical research operations. If you have a robust research background and excellent communication skills, this is your chance to make a difference.

Key Responsibilities:
• Coordinate clinical trials ensuring compliance with protocols
• Review study materials and document nursing responsibilities
• Perform health assessments and manage trial-related procedures




• Track investigational products and maintain their conditions
• Engage with interdisciplinary teams for successful trial outcomes

Requirements:
• Registered Nurse with at least three years of experience
• Proven skills in administering IV medications and drawing blood
• Excellent interpersonal, verbal, and written communication skills
• Experience in clinical cognitive testing preferred
• Proficiency with MS Office applications

Make a meaningful contribution to research that enhances healthcare delivery at Bruyère Health.
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📌 Research Project Coordination Role at Bruyère (Quebec City)
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📍 Quebec City