Bruyère Health Research Institute·Ottawa, Ontario
The Research Coordinator will manage day-to-day activities for neuromodulation clinical trials, including participant recruitment, data collection, and regulatory compliance. They will also provide administrative and financial support, such as budget tracking, meeting coordination, and drafting research reports.
Position type: Full-time, 75 hours / pay period, 1 FTE
$34.36 to $39.18 per hour
Closing Date: 2026/09/09*
Why should you join Bruyère Health RI?
The Bruyère Health Research Institute supports investigators who contribute to a better, more responsive health care system that delivers the best care to patients, residents, and families. We focus on finding the future of care for aging Canadians and vulnerable populations.
Summary of the role
We are looking to hire a Research Coordinator to join our Palliative Care research team led by Dr. James Downar. The successful candidate will be responsible for coordinating day-to-day activities in neuromodulation clinical trials (e.g., Scrambler Therapy (ST) for neuropathic pain and repetitive transcranial magnetic stimulation (rTMS) for psychological distress), including Health Canada and Research Ethics Board submissions and adherence, participant recruitment, data collection and entry, and budget tracking.
Main duties and responsibilities
Other duties as assigned
Other duties as assigned
About Bruyère Health RI
Bruyère Health and its Research Institute are fully affiliated with the University of Ottawa, and have other regional academic, government, NGO, and industry partners engaged in collaborative research and innovation initiatives. Our research priorities include Aging and Long-Term Care, Palliative Care, Rehabilitation and Recovery, and Social Accountability (encompassing Primary Care and Health Equity).
*Please note that applications received after the closing date will not be considered.
This posting is intended to fill an existing vacancy.
All applicants must provide a recent CV, and a cover letter that clearly indicates that they meet the required qualifications. Copies of your degrees and certifications, if applicable, in one of Canada’s official languages must also be included. Should it be determined that any background information provided is misleading, incorrect, or inaccurate, Bruyère Health may, at its discretion, dismiss your application.
Bruyère Health uses artificial intelligence to screen and assess answers provided by applicants. All applications received are subsequently reviewed by a member of our team. The information received, including that which is reviewed and analyzed by artificial intelligence, is used and stored in a secure environment and in accordance with Bruyère Health’s privacy policy PHIL 04 - Privacy and Confidentiality of Personal Information.
Bruyère Health promotes the principles of diversity and inclusion and adheres to the Employment Equity Act and Accessibility for Ontarians with Disabilities Act. Bruyère Health is committed to developing inclusive, barrier-free selection processes and work environments. If contacted regarding this competition, please advise the departmental official of the accommodation measures which may be required to enable you to be assessed in a fair and equitable manner.
All Bruyère Health employees are required to provide proof of full vaccination for all identified communicable diseases as per our Communicable Diseases: Health Surveillance and Management policy.
An acknowledgement of receipt will be sent following the submission of your application. We thank all applicants for their interest, however, only those selected for further consideration will be contacted.
The next step is yours, apply now!
Candidates must hold at least an undergraduate degree in a relevant health science field and possess a minimum of two years of clinical research experience. Essential qualifications include experience with Health Canada regulated trials, REB applications, and knowledge of GCP guidelines.
Market context
Research Coordinator opportunities in Ontario commonly seek candidates who can manage clinical studies, Health Canada–regulated trials, REB applications, and GCP requirements; relevant degrees and hands-on experience can make applicants more competitive. Before applying, prepare examples of your trial coordination and regulatory work, and use the AI-summarized requirements and benefits from the original job description here to reduce research time, including pension, wellness, mental health, and family assistance supports.