Alagille Syndrome Alliance jobs and careers
As of October 23, 2026, Alagille Syndrome Alliance has no open roles listed.
About Alagille Syndrome Alliance
"Mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille Syndrome." The Alagille Syndrome Alliance is a 501(c)(3) public charity with a Medical Advisory Board, a quarterly newsletter and web site that reachs families worldwide. We provide a vital link between families and offer them the resources they need to help their children live longer and healthier lives. The ALGSA is the primary resource for people with ALGS, their families and friends who form a close-knit community to provide mutual support, share information, and connect to resources. As the source of current, accurate information on ALGS and its treatment, we provide financial support for research and are actively involved in encouraging our members to participate in research studies.
- Employees
- 1 to 10
Leadership
The top of Alagille Syndrome Alliance's org chart, with how many people report into each leader.
Roberta Smith
President
Jobs at Alagille Syndrome Alliance
No open positions right now. Explore more companies on TheJobsMap.
Alagille Syndrome Alliance jobs: common questions
- Is Alagille Syndrome Alliance hiring right now?
- Alagille Syndrome Alliance has no open roles listed as of October 23, 2026. Roles appear here as soon as they are posted on Alagille Syndrome Alliance's careers site.
- Who leads Alagille Syndrome Alliance?
- Roberta Smith, President, is at the top of Alagille Syndrome Alliance's org chart.
- How do I apply for a job at Alagille Syndrome Alliance?
- Pick a role on Alagille Syndrome Alliance's TheJobsMap page and select Apply. Every listing links to the original posting on Alagille Syndrome Alliance's own careers site, so you apply directly with the employer.