PSPA is hiring a Research Coordinator for a 12-month maternity cover with a biomedical science degree or relevant experience.

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🚨*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?…

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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

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