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A leading healthcare institution in London is seeking a HCPC-Registered Clinical Scientist to analyze whole-genome sequencing data. The successful candidate will contribute to diagnostic reporting and work closely with clinicians to integrate findings into patient care. HCPC registration and experience in a diagnostic genetics laboratory are essential. This is a 14-month funded position with professional development opportunities.
The Neurogenetics Unit of the National Hospital for Neurology and Neurosurgery provides a regional molecular genetic service for inherited neurological disease and a national and international diagnostic service for rare neurogenetic disorders. It is merged with the Regional Genetics Laboratory at Great Ormond Street Hospital to form the lead Rare Disease Laboratory in the North Thames Genomics Laboratory Hub. The laboratory is ISO accredited and works closely with clinicians and research groups at the UCL Queen Square Institute of Neurology.
University College London Hospitals NHS Foundation Trust (UCLH) is one of the most complex NHS trusts in the UK, serving a large and diverse population. We provide academically led acute and specialist services across eight sites:
UCLH specialises in women’s health and the treatment of cancer, infection, neurological, gastrointestinal and oral disease. It has world-class support services including critical care, imaging, nuclear medicine and pathology.
An exciting opportunity has arisen for a HCPC-Registered Clinical Scientist to join our team of Clinical Scientists. The post is funded for 14 months initially. The successful candidate will focus on the analysis of whole-genome sequencing data, with opportunities to work in other areas.
For the full Person Specification and more information regarding the main responsibilities of this role, please refer to the attached Job Description.
This advert closes on Tuesday 25 Nov 2025