Overview

This post will work across the life span of both Paediatric and Adult Cystic Fibrosis patients. The post holder will provide social work services that meet the needs of children, adolescents and adults with CF and their families, in line with the Regional Cystic Fibrosis Clinical Network and national best‑practice guidelines.

The core responsibility is to support patients and families in managing psychosocial, practical and health‑related challenges, including the impact of CF at key stages such as diagnosis, transition, deteriorating health, transplantation and end‑of‑life care. The role links the paediatric and adult services to provide a seamless, patient‑centred experience.

Key Responsibilities

• Manage a caseload of children’s and adult CF patients across inpatient, outpatient and community settings.
• Undertake holistic psychosocial assessments and develop care plans in partnership with patients and families.
<...