Specialist in Precision Genetics

3 weeks ago


London, Greater London, United Kingdom Novo Nordisk Full time

Position Overview

We are seeking a highly skilled and innovative Genomic Precision Medicine Specialist to leverage advanced human genetics insights to enhance trial outcomes and facilitate human-genetics-driven precision medicine for Rare Diseases.

Key Responsibilities:

  • Provide genetic expertise to project teams focused on advancing therapies through the drug development pipeline.
  • Collaborate with colleagues to pinpoint how genetics can inform critical decisions, such as indication selection and target population identification.
  • Integrate genetic data with other omics disciplines—proteomics, metabolomics, transcriptomics, and epigenetics—to deepen understanding and tailor treatment responses.
  • Utilize trial data alongside genetic information to guide decision-making and identify populations most likely to benefit from our scientists' developed treatments.

In this role, you will have the opportunity to initiate and lead your own projects while also contributing your expertise to ongoing initiatives within the Human Genetics Centre of Excellence (CoE). Our research environment promotes collaboration, allowing you to work alongside statistical geneticists, clinicians, and computational and laboratory scientists, both internally and with external partners, to ensure optimal treatment delivery.

Qualifications:

We invite applications from candidates who demonstrate a strong team spirit, meticulous attention to detail, and a passion for thriving in a dynamic, fast-paced environment that encourages creative independence and knowledge sharing. A keen interest in applying your expertise to drug development is essential.

We are particularly eager to connect with candidates possessing:

  • A Ph.D. in human genetics, statistical genetics, genetic epidemiology, pharmacogenomics, or related fields, with notable contributions to impactful scientific publications.
  • Several years of postdoctoral experience in the genetics of rare diseases, preferably in rare blood and/or endocrine disorders.
  • Proficiency in high-performance computing systems and programming languages for analyzing large-scale datasets, such as R or Python.
  • Experience with large-scale genetic datasets and GWAS, including marker-trait and gene-trait associations.
  • Strong communication skills for conveying insights and presenting concepts to diverse audiences.
  • A self-motivated approach and the ability to collaborate effectively within interdisciplinary teams.

Experience in managing omics data (e.g., transcriptomics, proteomics) is advantageous, as is professional or postdoctoral experience in analyzing clinical trial data within academia or the biotech/pharma industry.

Department Overview:

You will join our Translational Genomics & Precision Medicine Department, part of the Human Genetics Centre of Excellence (CoE), led by Vice President, Joanna Howson PhD. The CoE's mission is to harness data science and human genetics to discover and develop new drug targets and biomarkers through various human-centric methodologies.

About Novo Nordisk:

As a leading life-science company, we are driven by our commitment to improving lives. Our work is inspired by the complexities of life, and we strive to empower individuals to lead lives free from chronic diseases.

Application Process:

Interested candidates are encouraged to submit their applications through our careers portal. We are committed to an inclusive recruitment process that values diversity and equality of opportunity for all applicants.



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