Haematology Clinical Nurse Specialist/BMT Coordinator
| Dyddiad hysbysebu: | 17 Mawrth 2026 |
|---|---|
| Cyflog: | £47,810.00 i £54,710.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £47810.00 - £54710.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 30 Mawrth 2026 |
| Lleoliad: | Norwich, NR4 7UY |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | C9234-26-0208 |
Crynodeb
Clinical: To assess, plan, deliver and evaluate care for patients with haematological disorders in order to ensure that high standards of evidence-based care are provided. To provide information, support, advice and specialist knowledge to patients, their families and carers at all stages of the patients care pathway. This may be verbal and/or written. To act as a point of contact for patients, their families and carers, by attending outpatient clinics, the day unit and inpatient wards where necessary, and by other means of communication e.g. telephone and email. To act as the patients advocate, especially when discussing treatment options and possible involvement in clinical trials, so that patients can make an informed choice. To liaise closely with all members of the multi-professional team, including medical staff, ward Nurses and other Nurse Specialists, to ensure continuity of patient care. To establish and maintain effective communication with patients, their families and carers, and all members of the multi-professional team including those from primary care and other outside agencies. To participate in and develop Nurse-led clinics with focus on all aspects of BMT service. Line Management/Financial Management Responsibilities: Actively contribute to the review and development of relevant directorate policies, guidelines and protocols, with particular preference to the development of nursing in line with local and national developments. Prepare the monthly Finance reports for BMT. Act as a positive role model. Research: To be aware about and participate in clinical research trials, liaising closely with medical and nursing staff, as well as the local research network and clinical trials team, to ensure that patients and their families are fully informed, thus enabling informed consent. Participate in the collection of data and specimens for clinical trials. Please see the attached job description for full details.