South East Genomics

WORK FOR US

Are you looking to join one of the largest providers of genomic testing in the UK? Would you like to join a network of staff across South London, Kent, Surrey and Sussex in providing an equitable genomic service for all NHS patients?

The South East GLH has a wide range of roles and any vacancies will be listed below.

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South East GLH Scientific Lead for Cancer Genomics

We are offering a fantastic 8b opportunity for a senior scientist with a strong background in translational science and/or diagnostic test development.

The successful candidate will take on a senior leadership position at the South East GLH and within the Cancer Genetics Service to implement state-of-the-art tumour diagnostics and ensure that the GLH stays at the cutting edge of cancer patient care.

Go to the vacancy page

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South East Genomics

Welcome to our new home

We have recently changed our name from the NHS London South Genomic Laboratory Hub to the NHS South East Genomic Laboratory Hub. We think it better reflects the region we cover!

Read the full announcement here
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With any Whole Genome Sequencing (WGS) test ordered, a Record of Discussion (RoD) form will also need to be submitted. This document is to record the patient’s consent for genomic testing and their choice on taking part in research. Guidance on the patient choice conversation can be found here. 
 
This RoD form will be available for clinicians to download from this webpage. Once completed with the patient, it can be send to the lab with the corresponding test order form and sample.
Tests available to order will be listed in the National Genomic Test Directory. A test order form will soon be made available for clinicians on this webpage to download and complete. This form will include the address of the laboratory that the appropriate sample and completed form needs to be sent to.
 
Until the new Genomic Laboratory Service goes live, please continue to follow existing test order processes.
 
Later this year, the online test ordering tool for Whole Genome Sequencing will be integrated into the National Genomics Informatics System (NGIS) and clinicians will be able to search or filter to find a clinical indication, confirm eligibility criteria and start the test request process for their patient.