Exeter is home to a thriving genomic medicine community, with career options available at every level within the Department of Clinical and Biomedical Sciences – see https://medicine.exeter.ac.uk/clinical-biomedical/careers/. We currently have a number of opportunities in rare disease genomics:
Postdoctoral researcher to evaluate approaches to newborn screening with whole genome sequencing using large-scale population cohorts (MRC funded).
Postdoctoral researcher to apply machine-learning approaches for improving rare variant interpretation and burden testing for discovery of novel disease genes (Wellcome funded).
Clinical genomic scientist and postdoctoral bioinformatics positions jointly between the University of Exeter and the NHS Royal Devon & Exeter Hospital to develop new approaches to rapid whole genome sequencing in diagnostics (NHS funded).
Come and join our friendly team and make a real difference to how genomics is used in medicine! Please contact (caroline.wright [at] exeter.ac.uk) to discuss!
