Full-Time

Associate Director of Development

The ALS Association

The ALS Association

201-500 employees

Advances ALS research and supports patients

Compensation Overview

$68.5k - $83.2k/yr

Houston, TX, USA

Remote

Remote role based out of the Houston, TX metro area; candidate may need to be within the Houston metro region.

Category
Business & Strategy (1)
Required Skills
Adobe Photoshop
Word/Pages/Docs
Salesforce
Adobe Illustrator
Data Analysis
Excel/Numbers/Sheets

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Requirements
  • Bachelor’s degree, required.
  • A minimum of 3-5 years of recent and relevant fundraising and event production experience with proven history of achieving revenue goals.
  • Strong knowledge of the Southwest communities and corporate leaders is a plus.
  • Proven managerial experience; ability to effectively coach, delegate and manage responsibility; knowledge of general human resources practices
  • Must have extensive experience in fundraising and fundraising mechanics including CRM or other donor management, communications, and fundraising platforms
  • Demonstrated ability to provide leadership, organize fundraising activities effectively, and participate in high-level customer service support
  • Demonstrated ability to incorporate latest peer-to-peer fundraising tools into the event experience required
  • Maintains strong organizational, detail and interpersonal skills
  • Excellent written communication, public speaking, and customer service skills
  • Demonstrated proficiency with a variety of computer programs in a Windows environment, such as Microsoft Word, Excel, and PowerPoint. Ability to quickly train and use a donor database (such as Salesforce).
  • Proficiency with video conferencing software.
  • Experience using Quark, Illustrator, Publisher and/or Photoshop a plus, to produce and/or edit program-specific materials to meet deadlines.
  • Must effectively respond to constantly changing priorities and effectively respond to and proactively resolve problems/conflicts as they arise; the ability to “think on one’s feet” is critically important
  • Great relationship and interpersonal skills; loves working with people and proven ability to build and manage relationships that help advance an organization’s mission through fundraising and donations
  • Goal-oriented and high degree of self-initiative, motivation and discipline
  • The ability to travel up to 50% of the time and work occasional nights and weekends for Association business and events
  • Ability to occasionally bend, lift and carry equipment and other materials (up to 30 pounds)
Responsibilities
  • Lead all aspects of the revenue/fundraising within defined portfolio. Including but not limited to developing engagement and fundraising strategies that drive revenue, budget management, donation tracking, logistical planning, and execution.
  • Assist with the implementation of strategies to meet all fundraising goals for the territory.
  • Provide coaching and direction to Development Managers as needed to meet fundraising goals.
  • Cultivate and steward relationships with key constituents and help create a pipeline of donors for mid-level and major gifts.
  • Provide volunteer support through face-to-face meetings, phone and email contact, speaking engagements as requested, kick off events, and corporate cultivation meetings
  • Along with Corporate Development staff, grow corporate partnership initiatives including prospecting, cultivation, developing custom proposals, securing commitments, stewardship, and retention.
  • Work closely with the Team Captains and participants to develop their personal and team fundraising plans by mentoring, coaching, and encouraging fundraising efforts.
  • Maintain a portfolio of individual donors specific to the Southwest area, prospecting, cultivating, soliciting, and stewarding annually.
  • Responsible for the recruitment, stewardship and retention of event committee chair and members as well as building strong relationships with community partners.
  • Analyze fundraising data from assigned events to forecast revenue, as well as surface areas of opportunity and challenge.
  • Work in conjunction with the Marketing and Communications team to help execute all marketing communication efforts relating to local and community events in respective region.
  • Manage the Convio database, Team Raiser, Salesforce, and/or Greater Giving platform to track financial progress.
  • Maintain knowledge of fundraising trends, technologies, and strategies within the charitable event field
  • Actively look for and take action to incorporate “moves management” (cultivation, solicitation, renewed contributions, moving donor from lower level to higher level) as part of stewardship.
  • Where opportunity presents itself, work closely with embedded staff to actively cultivate and when appropriate solicit donors for planned gifts and/or major gifts.
  • Perform other duties as assigned in support of mission and fundraising goals.

The ALS Association is a national nonprofit organization dedicated to fighting ALS on multiple fronts. It leads global research efforts, provides assistance to people with ALS through a nationwide network, coordinates multidisciplinary care via certified clinical care centers, and builds government partnerships to advocate for policies and funding. Its programs include funding and guiding research, offering patient and caregiver support, coordinating clinical care to ensure access to specialized services, and advocating for public policy and resources. This approach is distinct because it combines research leadership, direct services, and policy advocacy under one umbrella, with a nationwide network and dedicated ALS Nexus platform to connect patients, researchers, and clinicians. The goal is to discover new treatments and a cure for ALS while improving quality of life and expanding access to care for those affected.

Company Size

201-500

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

1985

Get referred to The ALS Association

See people who can refer or advise you

Simplify Jobs

Simplify's Take

What believers are saying

  • Walk to Defeat ALS expands fundraising and community engagement.
  • University of Miami partnership showcases promising genetic treatment progress.
  • Hoffman Clinic Awards extend coordinated care into underserved communities.

What critics are saying

  • ALS remains fatal, sustaining long-term donor fatigue pressure.
  • Only half of registered patients receive coordinated care, exposing rollout failures.
  • Research breakthroughs can stall, weakening credibility and high-value donor retention.

What makes The ALS Association unique

  • Largest philanthropic funder of ALS research worldwide.
  • Combines research, care, advocacy, and family support nationwide.
  • Operates certified clinical care centers and multidisciplinary care networks.

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Benefits

Health Insurance

401(k) Company Match

Disability Insurance

Life Insurance

Wellness Program

Paid Vacation

Paid Holidays

Company News

The ALS Association
Jun 29th, 2026
Statement from the ALS Association on Chris Johnson's ALS Diagnosis.

Statement from the ALS Association on Chris Johnson's ALS Diagnosis. Arlington, Va. (June 29, 2026) - We are deeply moved by the courage Chris Johnson has shown in sharing his ALS diagnosis with the world. We stand with Chris, his wife Brittany, and their family as they navigate this incredibly difficult journey. "I still think the same. I still dream. I still love my family. My body just doesn't cooperate." Chris's words capture something we hear from so many people living with ALS. We are inspired by his determination to fight, and by his commitment to using his platform to raise awareness for the ALS community. What people need to know about ALS: * ALS is a fatal neurodegenerative disease that gradually takes away a person's ability to walk, speak, swallow, and eventually breathe. It affects the motor neurons in the brain and spinal cord that control voluntary movement. As those neurons deteriorate and die, the brain loses its ability to initiate and control muscle movement. * ALS does not discriminate. As Chris noted, his case is sporadic ALS - meaning it occurred with no family history. About 90% of all ALS cases are sporadic. * Every 90 minutes, someone in the United States is diagnosed with ALS - and someone loses their battle with it. * The ALS Association has a strategic plan to make ALS livable and cure it. To get there, we need to accelerate research, optimize current treatments and care, and reduce the harms of ALS. * ALS can be difficult to diagnose. There is no single test that confirms ALS. Because its early symptoms - muscle weakness, slurred speech, difficulty gripping - can resemble other conditions, people often see multiple specialists before receiving a confirmed diagnosis. This delay can mean lost time for treatment and support, which is why the ALS Association developed the thinkALS tool to help clinicians identify and refer patients to ALS specialists sooner. * There is currently no cure for ALS, and it is fatal. The typical life expectancy following a diagnosis is typically two to five years, though every journey is unique. * Research is making promising advancements and there is real reason for hope. We invested in early antisense technology which led to development and FDA approval to Qalsody (tofersen), the first-ever gene-targeted therapy for ALS. There is evidence that Qalsody(R) may not just slow disease progression, but in some cases help reverse some of the lost function, something that scientists did not think possible. * Chris has said he is participating in a clinical trial, reflecting the growing pipeline of promising treatments the ALS Association is proud to help fund. We are committed to accelerating the path from scientific discovery to treatments that reach every person living with ALS. Our mission - and how you can help. The ALS Association's mission is to make ALS livable and cure it. Here is how you can make a difference: * Learn more about ALS and share Chris's story * Donate to ALS research * If you or a loved one has been diagnosed, contact us. The ALS Association offers care services, support groups, and connections to certified treatment centers across the country. * Call our helpline at 1-800-782-4747 or visit ALS.org To Chris: thank you for choosing to fight - not just for yourself, but for the tens of thousands of Americans living with ALS today. We are honored to walk this road alongside you. About the ALS Association The ALS Association is the largest ALS organization in the world. The ALS Association funds global research collaborations, assists people with ALS and their families through its nationwide network of care and certified clinical care centers, and advocates for better public policies for people with ALS. The mission of the ALS Association is to make ALS livable and cure it. For more information about the ALS Association, visit our website at www.als.org. About ALS Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. Over the course of the disease, people lose the ability to move, to speak, and eventually, to breathe. The disease is always fatal, usually within five years of diagnosis. Few treatment options exist, resulting in a high unmet need for new therapies to address functional deficits and disease progression. Manager, Communications June 29, 2026 Article Topic ALS Mission ALS Awareness