Postdoctoral Scientist Myeloid Cancer Biology

Duration: 3 years fixed term

About the role:

We are seeking a Postdoctoral Scientist to join the newly established Myeloid Cancer Biology group, led by Dr Justin Loke, to investigate how inherited and acquired genetic mutations cooperate to drive acute myeloid leukaemia (AML) and myelodysplastic syndrome (MDS).

A key focus of the post are inherited conditions caused by germline mutations that carries a substantial lifetime risk of AML/MDS. How specific combinations of somatic mutations cooperate with these inherited mutations to drive leukaemic transformation remains poorly understood, in large part because existing model systems cannot recreate the complex, multi-mutation genotypes seen in patients.

The post holder will use a novel transgenic mouse platform developed by the PI and colleagues, in which Cas12a-mediated genome editing enables simultaneous disruption of up to four genetic loci within single haematopoietic stem and progenitor cells. Using this platform, the post holder will generate and characterise genetically complex murine models of inherited predisposition related MDS/AML, combining in vivo transplantation experiments, flow cytometry and histopathology with single-cell multiome (RNA and ATAC) profiling to define the epigenetic programmes underlying malignant transformation, and to establish proof-of-concept for novel therapeutic vulnerabilities in this and related inherited myeloid malignancy syndromes.

This post is supported by a John Goldman Fellowship from Leukaemia UK.

The Environment:

The Myeloid Cancer Biology group was established in October 2025, and this post offers an early opportunity to help shape a new laboratory's research programme and infrastructure. The post holder will work closely with the Group Leader and benefit from the wider myeloid malignancy and haematology community at the Institute, including collaboration with Professor Tim Somervaille (epigenetic mechanisms in myeloid neoplasia) and Professor Georges Lacaud (RUNX1 biology and haematopoiesis), aswell as an established international collaboration on Cas12a genome-editing technology.

The Institute's core facilities – including the Genome Editing and Mouse Models Facility, Flow Cytometry, Molecular Biology and Computational Biology Support – provide direct technical support for the in vivo and single-cell components of this project. The group is based in the Paterson Building, directly attached to The Christie NHS Foundation Trust, providing a translational research environment with strong links to clinical haematology.

About you:

You should have, or be near completion of, a PhD in cancer biology, molecular biology, genetics, immunology, haematology or a related field. You will have demonstrable practical experience of mammalian cell culture and core molecular biology techniques, together with a track record of scientific publication or presentation, and the ability to define and solve research questions independently. Prior experience with murine/in vivo models, genome engineering or CRISPR-based approaches, and/or single-cell genomic technologies would be a strong advantage, as would a background in haematopoiesis or leukaemia biology – but candidates with strong complementary expertise and a genuine interest in developing these skills are also encouraged to apply.

How to apply?

For any informal enquiries about this post, please contact Dr Justin Loke email: justin.loke@cruk.manchester.ac.uk

Closing date: 18:00, 11 October 2026 Sunday

First-round interviews (via Microsoft Teams): 15 and 16 October 2026

Second-round interviews (in person): w/c 26 October 2026 

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