Cancer Research UK appoints Professor Mariam Jamal-Hanjani as Chief Clinician

The thoracic oncologist and TRACERx investigator takes up the newly prominent role as CRUK's scientific leadership structure evolves.

Published · AI-drafted summary based on 2 public sources
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Cancer Research UK has appointed Professor Mariam Jamal-Hanjani as its new Chief Clinician. Jamal-Hanjani is a consultant oncologist and professor at University College London, widely known for her leadership of the TRACERx lung cancer evolution study, which has produced a series of landmark findings on tumour heterogeneity, clonal dynamics, and the genomic basis of metastasis.

The role of Chief Clinician is intended to bridge CRUK's research strategy with clinical translation and health-system engagement. In an accompanying profile published by CRUK, Jamal-Hanjani described her priorities as spanning early detection, treatment science, and ensuring that research findings reach patients equitably.

The appointment is of note to the genetics and genomics research community given Jamal-Hanjani's track record in longitudinal tumour sequencing and her advocacy for integrating multi-region genomic profiling into the design of cancer trials. Her elevation to a senior leadership position at the UK's largest cancer research charity signals continued institutional investment in cancer genomics as a translational priority.

Sources

Read the original reporting — these are the public sources this summary draws from.

  1. Primary source Cancer Research UK · 2026-10-06
    Cancer Research UK appoints Professor Mariam Jamal-Hanjani as its new chief clinician
  2. Cancer Research UK · 2026-10-06
    A moment with Mariam: Meeting CRUK's new Chief Clinician

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cancer-research-uk cancer-genetics cancer-genomics tracerx tumour-heterogeneity science-leadership
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Educational summaries of public genetics news

Genetic Current is the news section of Evagene, an academic, research, and educational pedigree-modelling platform. Stories are AI-drafted summaries of items from trusted public sources, written for researchers, clinicians, educators, students, genealogists, and patients with an interest in genetics. Summaries are for educational and research purposes only and are not medical advice.

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