An exciting opportunity has arisen for a Regional Fundraiser to join the Fundraising Team at the Motor Neurone Disease Association based in either London or the Thames Valley.
Salary: c.£28,500 + London weighting plus benefits
Location: Home-based in region
Hours: Full-time 37 hours per week
Contract Type: Permanent
About the role
This role works with high profile supporters as well as a fantastic network of voluntary branches and groups, working across all elements of the fundraising teams within the regions.
The role is full of varied and interesting fundraising activities from promoting participation of local and national events, to attending functions on behalf of the Association, in order to meet agreed income and maximise the return of investment of fundraising activities.
What are we looking for?
You will have demonstrable experience of working within 'community' or 'relationship fundraising'. Outstanding communication and presentation skills are essential along with a proven track record in achieving fundraising targets.
We are looking for a people orientated self-starter with good organisational skills and the ability to work swiftly and methodically to ensure fundraising opportunities are seized and maximised.
A full driving licence and access to a car is essential
Travels expenses will be covered for this post.
How to apply?
We would love to hear from you.
If this sounds like the perfect opportunity for you, apply online now.
The MND Association was founded in 1979. Our mission is to improve care and support for people with MND, their families and carers. We also fund and promote research that leads to new understanding and treatments and brings us closer to a cure for MND. The Association also campaigns and raises awareness so the needs of people with MND, and everyone who cares for them, are recognised and addressed by wider society.
- MND is a fatal, rapidly progressive disease that affects the brain and spinal cord
- It attacks the nerves that control movement: people can still think and feel but their muscles refuse to work
- Six people die from MND every day in the UK. It has no cure
Please submit your application as soon as possible; due to the high volumes of applications we receive, and we reserve the right to close any adverts before the closing date once we have received sufficient applications.
Please note, from late 2019, our National Office will be relocating to new premises within Northampton.
At the MND Association we are committed to equalities and value diversity. We are working hard to remove perceived and actual barriers to participation by people with and affected by MND, current and future staff and volunteers and stakeholders.