What we offer
Generous annual leave entitlement (37 days – 25 days annual leave plus 12 days public holidays (pro rata)
Contribution pension scheme
Flexible hybrid approach to work
About the role
Are you looking for a role in which you will help to improve the lives of families in your community and beyond? One
that encourages you to share your expertise, build new skills and feel valued by colleagues, clients and the
organisation you work for?
We are looking for a part-time Admin/Resource Worker to join our Lanarkshire service.
Providing support to the Huntington’s Disease Specialist team, the part-time Admin/Resource Worker has a key role to
play in the specialist team which provides care management, specialist assessment and emotional support to
individuals and their families throughout Lanarkshire.
The service works in partnership with, and provides training and education to, local Health and Social Care teams in
addition to professionals and voluntary agencies involved in all aspects of Huntington’s disease care.
We invite applications from candidates with administration experience and excellent communication, IT and
interpersonal skills. You will be competent in using databases and spreadsheets and have a working knowledge of
NHS IT applications and audio typing. You will also be able to carry out basic budgetary tasks, manage the HD
Specialist Service diary and take minutes of meetings.
We are looking for someone who is enthusiastic, motivated and takes great pride in the work they do.
This is an exciting time to join Scottish Huntington’s Association as we enter the second year of of Standing Tall:
A Strategy For Growth 2023 – 28 to transform the care and support of Huntington’s families. The launch of
our five-year strategy followed two years of expansion in specialist teams, increased funding, a rise in media
engagement and growth in parliamentary support for our work.
Please note: Hybrid working means many of our staff work partially from home however it is expected that the post
holder will travel to the office based in Hunter Health Centre in East Kilbride as required during their work
week.
About Scottish Huntington’s Association
People impacted by Huntington’s disease need specialist services to cope with a severe and complex disease, the
impact on families and a lack of awareness amongst health and social care providers and the wider public.
Scottish Huntington’s Association is the only charity in the country exclusively dedicated to providing expert and
personalised support for those impacted by Huntington’s disease.
Our personalised support reduces unnecessary hospital admissions, supports carers and other family members; lowers
household poverty; and alleviates wellbeing risks to children and young people living in Huntington’s
families.
We are commissioned by NHS Boards and Health and Social Care Partnerships throughout the country to share our
expertise with front line staff and build support for improved services and higher standards of care for every
family impacted by this devastating disease.
About Huntington’s disease
Huntington’s disease is caused by an inherited faulty gene that damages the brain over time. People with the disease
can eventually lose the ability to walk, talk, eat, drink and care for themselves, requiring specialist support
from those who understand the condition.
The disease is genetic, meaning it is passed down from one generation to the next. It therefore impacts entire
families over generations rather than individuals alone. Anyone with a parent who has Huntington’s has a 50%
risk of inheriting the condition from them.
Around 800 people in Scotland are living with the symptoms of Huntington’s disease right now. A further 3,200 are
estimated to be at risk of developing Huntington’s disease as a result of inheriting the faulty gene.