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Manager, Policy & Advocacy

This job is no longer available

Bethesda, MD, USA
Full-time

The Cystic Fibrosis Foundation seeks a Manager to join our Policy and Advocacy department in Bethesda, MD.  

This position is responsible for managing the Cystic Fibrosis Foundation’s nationwide volunteer advocacy program. The Manager will coordinate the recruitment and training of key volunteers and help develop messaging and strategy to mobilize these volunteers, both online and offline, to advance the CF Foundation’s public policy agenda. Additionally, the Manager will play a key role in planning and executing several large advocacy events throughout the year.

This position will assist in the planning and implementation of public affairs campaigns designed to promote access to care for cystic fibrosis patients and provide for increased access to specialized CF care and treatments for the disease.

This position will also collaborate with other teams within the organization, including Field and Communications Departments, on projects that help execute Foundation goals and objectives. As a member of the Policy and Advocacy team, this position will be tasked with special projects as needed.

Areas of Responsibility: 

As employees perform their roles and responsibilities, they are expected to demonstrate behaviors that are aligned with the Cystic Fibrosis Foundation’s Five Core Values including:

  • Keep sight of what really matters.
  • Aspire for excellence in all we do.
  • Stronger together.
  • Innovate with courage.
  • Care about our people.

Essential Functions:

  • Team Management
    • Manage the day-to-day activities of advocacy staff to execute work plans, volunteer engagement and training.
    • Manage cross functional and inter-departmental projects.
  • Volunteer Recruitment and Retention
    • Support a tiered national volunteer advocacy network to form and strengthen relationships with elected officials at the state and federal levels
    • Work with volunteer leaders nationwide and facilitate their efforts to coordinate local activity
    • Work with field staff to identify and recruit additional advocacy leaders
  • Communications and Messaging
    • Draft and edit materials advocacy materials and action alerts to help volunteer advocates and key stakeholders
    • Support and maintain advocacy database and web pages
  • Event Planning
    • Support, plan and execute four annual major advocacy events ranging from 50 to over 300 participants
    • Provide support to volunteers and chapter staff for state-level meetings

Additional Responsibilities:

  • Database management and analysis
  • Provide input on process, design and implementation of cross functional
Educational Background: 
Bachelor’s degree, preferably with a background in political science, communications, public policy, or biological science
Skills/Experience: 
  • 5-7 years of community/political organizing, communications, fundraising, or similar experience including 3-5 years supervisory experience
  • 3-5 years of experience recruiting, training, and managing volunteers
  • Ability and experience working collaboratively across functions among various subject matter experts
  • At least a basic familiarity with the legislative and political process.
  • HTML or equivalent proficiency preferred

Organization Info

Cystic Fibrosis Foundation

Overview
Headquarters: 
Bethesda, MD, United States
Founded: 
1957
About Us
Mission: 

The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment and ensuring access to high-quality, specialized care.

The Cystic Fibrosis Foundation has 70 chapters and branch offices across the country that work diligently to raise funds to help support the search for a cure. In addition, the Foundation provides funding for and accredits more than 120 CF care centers and 53 affiliate programs nationwide, including more than 100 programs for treating adults with CF. The high quality of specialized care available throughout the care center network has led to the improved length and quality of life for people with CF. Located at teaching and community hospitals across the country, these care centers offer the best care, treatments and support for those with CF.

Listing Stats

Post Date: 
Aug 23 2018
Active Until: 
Sep 23 2018
Hiring Organization: 
Cystic Fibrosis Foundation
industry: 
Nonprofit