NHC Job Bank

Section: 

The National Health Council has created this special page for its members to post job openings and to foster the unique talent pool of patient advocacy organizations. For more information on posting a job, click here.

 

Washington, D.C.
Posted: Tuesday, January 30, 2018

ROLE:

Arlington, VA
Posted: Tuesday, January 23, 2018

 

Washington, D.C.
Posted: Monday, January 22, 2018

Bring your passion and leadership to join the fight against ALS! 

Washington, D.C.
Posted: Wednesday, January 10, 2018

Founded in 1920, the National Health Council (NHC) is the only organization that brings together all segments of the health community to provide a united voice for the more than 133 million people with chronic diseases and disabilities and their family caregivers. Made up of more than 100 national health-related organizations and businesses, the NHC's core membership includes the nation’s leading patient advocacy organizations, which control its governance.

Washington, D.C.
Posted: Tuesday, January 9, 2018

Position Description: 

Reporting directly to the Chief Executive Officer (CEO), the Executive Assistant & Governance Manager provides administrative and governance support to the CEO. The manager is the primary point of contact for internal and external constituencies on all matters pertaining to the CEO and serves as a liaison to the Board of Directors and as the staff lead for all governance meetings within the organization.

Larchmont, NY
Posted: Monday, December 18, 2017

Barth syndrome (BTHS) is a life-threatening, genetic, multi-system disorder affecting almost exclusively boys and young men worldwide. The Barth Syndrome Foundation (BSF), in conjunction with our international affiliates, is the only worldwide organization dedicated to Barth syndrome. Since its founding in 2000, BSF has grown quickly into a leader among rare disorder foundations in the world.  It operates the following:

Towson, Maryland
Posted: Friday, December 8, 2017

Position Overview: The Immune Deficiency Foundation (IDF), founded in 1980, is the national non-profit patient organization dedicated to improving the diagnosis, treatment and quality of life of persons with primary immune deficiency diseases (PI) through advocacy, education and research.