
About NORD
The National Organization for Rare Disorders (NORD) is the leading independent nonprofit organization representing all patients and families affected by rare diseases. Join our team and gain hands-on experience in nonprofit development and corporate engagement while supporting NORD’s mission to improve the lives of those impacted by rare diseases.
The Opportunity
The Development Intern will provide critical support to NORD’s Development team in managing outreach, tracking sponsor benefits, and coordinating logistics for NORD’s main conference. This role is ideal for a detail-oriented individual who is comfortable with repeated outreach and follow-up, enjoys working collaboratively across departments, and is eager to learn about nonprofit development and event sponsorships.
This is an unpaid internship with a flexible schedule, lasting from May-August 2026 with flexibility to adjust start and end date based on student availability.
What You Will Do
Qualifications
Learning Opportunities
Working Conditions
This is a U.S.-based, fully remote, unpaid internship with a flexible structure and meaningful responsibility. Requires reliable internet access. Occasional virtual meetings with staff and sponsors will be scheduled during standard business hours.
We expect the internship to last from May-August 2026 with flexibility to adjust start and end date based on student availability.
NORD is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
#LI

The National Organization for Rare Disorders (NORD), a 501(c)(3) organization, is an independent patient advocacy organization dedicated to helping individuals with rare diseases and the organizations that serve them. NORD, along with its 350+ patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient support services.
NORD serves all stakeholders in the rare disease community, including patients and their families, patient organizations, researchers, medical professionals, medical students, and companies developing orphan products.
NORD also works closely with many government agencies, most notably the National Institutes of Health (NIH) and the Food and Drug Administration (FDA).
All NORD programs are focused on one ultimate goal: to improve the lives of individuals and families affected by rare diseases.
NORD is the official U.S. sponsor of Rare Disease Day, an international observance day held on the last day of February each year. Its goals are to raise awareness for rare diseases and improve access to treatment and medical representation for individuals with rare diseases and their families. To learn more, visit rarediseases.org/rare-disease-day.
To learn more, please visit the NORD website at www.rarediseases.org. You can also follow NORD on X at @RareDiseases.