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Royston, England, United Kingdom
Job reference: R-046148
Posted date: May. 31, 2019

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. We're proud to have a unique workplace culture that inspires innovation and collaboration. We believe in the potential of our people and you’ll develop beyond what you thought possible.

The new R&D Oncology organisation brings together early and late oncology teams, from discovery through to late-stage development, with oncology specific Regulatory and Biometrics groups.

You’ll be in a global pharmaceutical environment but also exposed to strong rigorous academic science. For example, every postdoc has an external academic mentor to ensure we are working and publishing at the highest level in a field. What’s more, you’ll have the support of a leading academic advisor, who’ll provide you with the guidance and knowledge you need to develop your career.

You’ll join AZ’s Genomics Initiative, which aims to analyse data from up to two million genomes through a network of academic collaborations, including genomic samples donated by patients in its clinical trials. This genome sequence data is linked to rich phenotypic records, including data on disease, drug response data and patient outcomes. Focusing on our core key therapeutic areas (oncology, respiratory, cardiovascular, renal and metabolic disease), this initiative is expected to provide novel insights into the biology of disease, identify and validate new targets for medicines, improve selection of patients for clinical trials and match marketed treatments to patients most likely to benefit. Using the power of genomics to better define disease supports our ambition to develop the most innovative and impactful treatments for patients. Genomics is foundational to our research and development and help us in the discovery of the next wave of targeted innovative medicines. Join us and you could play a role in enabling this.

This role in AZ’s Centre for Genomics Research (CGR) focusses on using whole exome sequencing data from the world-renowned UK Biobank to explore genetic resilience and loss-of-function carrier phenotypes, which are of interest because understanding these phenomena has the potential to yield insight into biology of and resilience to disease.

Genetic resilience refers to the situation whereby individuals whose genomes harbour bona fide dominant-acting pathogenic variants remain ostensibly healthy. One possible reason for this is ‘suppressor’ variant(s) that counteract the effect of the pathogenic variant. Furthermore, heterozygous carriers of some recessive loss-of-function disease alleles can exhibit a related or sub-clinical phenotype, although this is poorly understood for many recessive-acting genes.

You’ll work with the CGR Analytics & Informatics team using AZ’s advanced access to the UK Biobank, which combines genetic (genotyping and whole exome sequencing) and phenotypic data from over 500,000 individuals in an unprecedented combination of breadth and depth. The UK Biobank also provides an exemplar opportunity to apply advanced analytics including PheWAS and machine learning algorithms to address the goals of the project.

Your research will be supervised by Dr Keren Carss (Genome Analyst, AZ Centre for Genomics Research) and Dr Slavé Petrovski (VP and Head of Genome Analytics & Informatics), with external academic supervision from Dr Emma Davenport of the Wellcome Sanger Institute. You’ll have the opportunity to collaborate with world leading experts in large-scale human genetics, both within AZ and outside of the company. Your research will lead to high quality peer-reviewed publications and the opportunity to present at national and international meetings.

Education and Experience required:


• A Doctoral degree in human genetics, statistical genetics, bioinformatics, or other relevant discipline.

• Demonstrable expertise in analysis of large-scale human genetics sequencing data.

• Experience of programming, preferably in R, Perl or Python, and using high performance computing clusters (e.g., Slurm).

• Knowledge of genomics community algorithms and solutions. Interest in the potential of genomics to impact drug discovery.

• Proven communications skills, including writing of manuscripts and oral presentations


• Experience with application of advanced analytics, including machine learning, in genomics.

• Experience querying and analysing complex phenotypic datasets and electronic health records.

• Track record of first-authored work published in reputable scientific journals.

Skills and Capabilities required:

• Highly motivated, well organized and resourceful.

• Able to work well both as part of a team and independently.

• Excellent communication skills (both oral and written).

This is a 3 year programme.  2 years will be a Fixed Term Contract, with a 1 year extension which will be merit based.  The role will be based in Cambridge, UK, with a competitive salary on offer. To apply for this position, please click the apply link below.

Advert opening date – 31st May 2019 / Advert closing date – 9th August 2019

AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.

Postdoc Fellow - Exploring genetic resilience using 500K exomes

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