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Job Description & How to Apply Below
Working alongside Dr. James Downar, you will lead the day-to-day operations of clinical trials focused on neuromodulation. Responsibilities include Health Canada submissions, participant recruitment and data management. The ideal candidate will have clinical research experience and a relevant educational background.
Key Responsibilities:
• Develop and manage study documentation and materials
• Conduct participant recruitment and informed consent processes
• Perform data collection through assessments and monitoring
• Ensure compliance with ethical and regulatory standards
• Assist in drafting research publications and presentations
Requirements:
• Bachelor's degree in health sciences or related fields
• At least 2 years of relevant clinical research experience
• 1+ years in clinical trial coordination
• Experience with regulatory submissions
• Strong problem-solving and organizational skills
Join Bruyère Health to make a meaningful difference in patient care and research.
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