The Cystic Fibrosis Trust

Who we are

About us

Cystic fibrosis (CF) is a condition affecting around 11,000 people in the UK and 70,000–100,000 worldwide. As a genetic disorder, individuals will have CF from birth and for the rest of their life. 

Cystic Fibrosis Trust is the only UK charity dedicated to improving the lives of people living with CF. Formed in 1964, the Trust has continued to invest in cutting-edge research into the causes and treatments for the condition, campaigning for fast and equal access to transformational therapies and supporting improvements in the standards of clinical care. As an organisation, we have supported many of the major advances in CF research and healthcare. However, there is still much to be done.

Our mission

Our mission and our values underpin everything we do, as we unite for a life unlimited by cystic fibrosis for everyone affected by the condition.

Our culture and values

Our Values

Together

We work together to represent the diverse experiences of everyone affected by CF.

We are committed to making the Trust a truly inclusive workplace, where everyone feels they belong.

We build collaborative and supportive relationships with colleagues, stakeholders and people affected by CF, but we also challenge where needed. We proactively work with people who have a diverse range of expertise and experience.

Trusted

Our work can be trusted by everyone affected by CF, our supporters and CF professionals. We are informed by evidence, accelerating progress in CF.

We are professional, transparent and understand the impact of our actions, words and campaigns. Our beliefs and actions are rooted in being trustworthy, compassionate and caring.

Unstoppable

We thrive on innovation and will take brave but considered risks to overcome challenges. We champion the CF cause, pushing for changes that will improve the lives of people living with CF.

We are ambitious, determined and courageous. We are committed to delivering impact for people living with CF while also maintaining a healthy work/life balance.

Equality, diversity and inclusion policy

We welcome applications from individuals of all backgrounds and experiences. The cystic fibrosis community is diverse, encompassing people of all ages and backgrounds. We are committed to ensuring that this diversity is reflected on our Board. We are especially interested in hearing from those with lived experience of CF, disabled individuals, and candidates from Black, Asian, and minority ethnic communities, as well as LGBTQI individual