Your responsibilities: You will join our diagnostic Rare and Inherited Disease team who are committed to patient-centered service provision through accurate and timely data analysis, interpretation, and reporting of genomic information. Attention to detail is essential to ensure that patient results are delivered in a safe and efficient way in order to direct patient management and therapeutic decisions. Key components of the role will be: report authorisation and responsibility for service delivery in a specified area of the department including line management of scientists. Through collaboration with relevant management teams, you will contribute to the overall management and direction of the Department. You will also be involved in training and education within your section and in liaising with other healthcare professionals to develop and maximise the effectiveness of the service. What we are looking for: an HCPC registered scientist with considerable diagnostic laboratory experience; excellent clinical and scientific knowledge of human genetics and the ability to critically analyse and interpret complex scientific data; good communication and leadership skills. PhD or FRCPath Part 1 is desirable.