Research Associate

2 weeks ago


Cambridge, United Kingdom University of Cambridge Full time

Applications are invited for an enthusiastic and motivated post-doctoral scientist to join an active research team investigating the molecular pathogenesis of rare inherited cancer predisposition syndromes and epigenetic disorders. The project is based in the group of Professor Eamonn Maher at the Department of Medical Genetics, University of Cambridge and is funded for 3 years in the first instance.

The appointee will take genomic approaches to understand the molecular pathogenesis of rare inherited human disorders in order to develop new diagnostic approaches and identify potential therapeutic interventions. The work be mainly "dry lab" analysing genomic, epigenomic and/or transcriptional data generated within the laboratory and publically available genomic data repositories. Excellent facilities are available, and the Department of Medical Genetics prioritises a positive research culture.

Fixed-term: The funds for this post are available for 30 months in the first instance.

The interview date for the role is: To be confirmed

The University has a responsibility to ensure that all employees are eligible to live and work in the UK.


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