PSPA is hiring a Research Coordinator for a 12-month maternity cover with a biomedical science degree or relevant experience.
Public source
Publisher name
Public post
🚨*Applications close today!* 🚨 This is your final opportunity to join PSPA as our Research Coordinator (12-month maternity cover). Are you ready to make a real impact?…
Company
PSPA
Together we can stop Progressive Supranuclear Palsy and Corticobasal Degeneration.
- Industry
- Non-profit Organizations
- Location
- Milton Keynes, GB
- Company size
- 51–200 employees
About PSPA
PSPA is a national charity offering support and information to people living with the neurological diseases Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD), while funding research into the conditions. PSPA relies entirely on voluntary donations. Both of these conditions are caused by the progressive death of nerve cells in the brain, leading to difficulty with balance, movement, cognition, vision, speech and swallowing. At least 5,000 people are living with PSP & CBD in the UK at any one time, but this number could be more than 10,000 as many are misdiagnosed with other conditions. There is no cure and there are no effective treatments for these conditions, but therapies can help manage symptoms. Thanks to PSPA, no one need face a diagnosis of PSP or CBD alone. Our helpline can be contacted on 0300 0110 122, helpline@pspassociation.org.uk
See moreLatest activity
Latest activity from PSPA
4 signals
Presence & Recognition
PSPA attended the annual PSPA Golf Day this year with 19 teams and raised over £4,000 in total, with the winning team Two Putt Shakur
Research & Knowledge
PSPA published a new research paper exploring differences between people with Corticobasal Syndrome (CBS) and Alzheimer’s disease biomarkers, post-mortem examination, and underlying causes.
Presence & Recognition
PSPA is hosting an awareness event in Basildon, Essex on Thursday, 24 September, featuring health education and medical education.
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