About ALS Association

The ALS Association, founded to support individuals affected by amyotrophic lateral sclerosis (ALS), is a national nonprofit organization dedicated to providing patient services, advancing scientific research, and promoting public policy efforts to ultimately find a cure for the disease. With local chapters across the United States and primary offices in Washington, D.C., Calabasas Hills, California, and Chicago, Illinois, the organization offers critical support to individuals and families navigating ALS at the community level. The ALS Association has invested over $48 million into global research initiatives, partnering with top institutions to accelerate scientific discovery and treatment development. Its mission is supported by a wide network of donors, volunteers, and professionals who share a commitment to improving the lives of those living with ALS. As an employer, the ALS Association fosters a purpose-driven, collaborative, and compassionate work culture that values dedication and empathy. The organization seeks individuals who are passionate about nonprofit work, community engagement, and medical advocacy. Employees often work alongside healthcare professionals, researchers, and grassroots organizers, all aligned in the effort to create a world without ALS. The ALS Association’s impact is both local and global, making it a meaningful workplace for those committed to social impact and medical progress.