About ALS Society of Canada
Founded in 1977, the ALS Society of Canada (ALS Canada) and our provincial partners are dedicated to supporting Canadians living with ALS and investing in research to make ALS a treatable, not terminal, disease. We are a registered charity that receives no government funding – all of our services and research are funded through the generosity of our donors. Through the ALS Canada Research Program, we fund peer-reviewed research grants, foster collaboration and build capacity within Canada’s ALS research community, and participate in new areas of research where we are well-positioned to have an impact. Within Ontario, ALS Canada has a role similar to that of the provincial ALS societies providing services and support to help meet the needs of people living with ALS. ALS Canada advocates federally, provincially and locally for better government support and access within the healthcare system for people touched by ALS.
- Employees
- 11 to 50
- Headquarters
- Toronto
Leadership
The top of ALS Society of Canada's org chart, with how many people report into each leader.
Tammy Pighin Moore
Chief Executive Officer
28 reports
Christopher K. Pon
Vice President, Fund Development
8 reports
Jennifer Asselin
Vice-president, Marketing, Strategic Communications, And Knowledge Exchange
7 reports
David Taylor
Chief Scientific Officer
4 reports
Sonila Elezi
Director, Human Resources And Volunteer Services
2 reports
Anthony Battista
Vice President, Finance & Administration
1 report
Paulenia Ramlingum
Office Manager & Executive Assistant
Jobs at ALS Society of Canada
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