Leadership Team

The Executive Leadership Team works alongside the Board of Directors to set and influence our strategic direction, while providing leadership both within the organisation and externally, as ambassadors and thought leaders.

Chris Wigley

CEO

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Professor Matt Brown

Chief Scientific Officer

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Catherine Byers

Chief Financial & Performance Officer

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Jackie Kinsey

Chief People Officer

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Nick Maltby

General Counsel, Company Secretary and Data Protection Officer

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Parker Moss

Chief Ecosystems and Partnership Officer

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Rakhi Rajani

Chief Digital Officer

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Dr Augusto Rendon

Chief Bioinformatician

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Dr Richard Scott

Chief Medical Officer

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Pete Sinden

Chief Information Officer

Anna Tomlinson

Chief Communications & Engagement Officer

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Board

The Genomics England Board oversees all of our activities, ratifies all major decisions and sets the overall strategy for the organisation. Genomics England has several independent advisory committees that report to the board. These include the Ethics Advisory Committee, Science Advisory Committee, Data Advisory Committee, Access Review Committee, GeCIP Board and the Audit Committee.

Chris Wigley

CEO

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Baroness Nicola Blackwood

Chair

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Vikram Bajaj

Non-Executive Director

Professor Sir John Bell

Non-Executive Director, Chair of Scientific Advisory Committee

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Professor Ewan Birney

Non-Executive Director

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Professor Matt Brown

Chief Scientific Officer

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Roz Campion

Department of Health Director

Andrew Eland

Non-Executive Director

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Dr Annalisa Jenkins

Non-Executive Director

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Professor Michael Parker

Non-Executive Director; Chair of the Ethics Advisory Committee

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Lord David Prior

Non-Executive Director

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Dr Keith Stewart

Non-Executive Director

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Sir Jonathan Symonds CBE

Non-Executive Director

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Participant Panel

The Participant Panel sits at the heart of Genomics England and is made up of participants from the 100,000 Genomes Project, and parents or carers of people involved in this project. It is expanding to include patients and relatives from the GenOMICC COVID-19 study and NHS patients who give consent for their whole genome sequences and associated health data to be used for research in the Genomics England National Genomic Research Library.

The Panel acts as an advisory body to the Genomics England Board, working to ensure that the health data held by Genomics England is being looked after with respect and used in the best interests of our participants.

Jillian Hastings Ward

Chair of the Participant Panel

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Rebecca Middleton

Vice Chair

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Cecily Berryman

Participant Panel member

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Dr Latha Chandramouli

Participant Panel member

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Kate Grafton

Participant Panel member

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Andy Hart

Participant Panel member

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Peter Hopper

Participant Panel member

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Shelley Simmonds

Participant Panel member

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Ismael Kherroubi Garcia

Participant Panel member

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Leanne LeRiche

Participant Panel member

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Anthony Locke

Participant Panel member

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Dave McCormick

Participant Panel member

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Helen Mendis

Participant Panel member

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Dominique Stephens

Participant Panel member

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Dr Charles Steward

Participant Panel member

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Helen White

Participant Panel member

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Science Advisory Committee

Our independent Science Advisory Committee advises the Genomics England Board on scientific aspects of the company's projects. This includes overseeing: disease inclusion criteria; Genomics England Clinical Interpretation Partnership (GeCIP) domain formation; data access request applications; and patient recruitment strategies. The Committee considers the interests of patients, the public, scientists and clinicians engaged in genomic research or genomic medicine.

Professor David Lomas

Deputy Chair, UCL

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Professor Sir John Bell

Non-Executive Director, Chair of Scientific Advisory Committee

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Professor Tim Aitman

University of Edinburgh

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James Brenton

Cancer Research UK Cambridge Institute

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Professor Sir John Burn

Newcastle University

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Professor Patrick Chinnery

University of Cambridge

David Church

Andrew Fry

Professor Dame Sue Hill

NHS England

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Professor Matthew Hurles

Wellcome Sanger Institute

Professor Mark Lawler

HDR UK

Professor Anna Schuh

University of Oxford

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Professor Matt Seymour

University of Leeds

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Dr Samra Turajlic

Cancer Research UK

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Professor Andrew Wilkie

University of Oxford

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Ethics Advisory Committee

Our independent Ethics Advisory Committee identifies, defines, examines and responds to ethical issues in the 100,000 Genomes Project. They also help to ensure the Project is delivered in the interests of the public and of participants.

They provide timely advice, guidance, review and recommendations on ethical issues, as requested by the Board.

Professor Michael Parker

Non-Executive Director; Chair of the Ethics Advisory Committee

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Professor Angus Clarke

Cardiff University

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Dr Sarah Chan

Usher Institute for Population Health Sciences and Informatics and University of Edinburgh

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Anne Croudass

Cancer Research UK

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Professor Bobbie Farsides

Brighton and Sussex Medical School and University of Sussex

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Alison Hall

PHG Foundation

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Alastair Kent OBE

Consultant in Health Policy and Patient Engagement in Rare and Genetic Diseases

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Professor Anneke Lucassen

University of Southampton

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Professor Penney Lewis

King’s College London

Dr Nadeem Qureshi

University of Nottingham

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Dr Anneke Seller

Health Education England

Shelley Simmonds

Participant Panel member

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Richard Stephens

Patient Representative & NCRI

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Dr Mark Taylor

Sheffield Institute for Biotechnology Law and Ethics and University of Sheffield

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Dr Ron Zimmern

PHG Foundation

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Access Review Committee

The Access Review Committee’s (ARC) role is to provide an independent examination and response to requests for access to genomic and health data held in the Genomics England National Genomic Research Library. These requests come from academic researchers, clinicians, and commercial researchers.

There is a set application process for these individuals to go through to access the data. The ARC reviews these applications to check that they are in line with the aims of the National Genomic Research Library Protocol and to assess whether they are in the interest of both the public and the participants. 

Professor Jonathan Knowles

Chair

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Jillian Hastings Ward

Chair of the Participant Panel

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Cecily Berryman

Participant Panel member

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Kate Grafton

Participant Panel member

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Peter Hopper

Participant Panel member

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Professor APS Hungin

OBE MD FRCP FRCGP FRSA

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Professor Dame Parveen Kumar

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Richard Stephens

Patient Representative & NCRI

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GECIP Board

The Genomics England Clinical Interpretation Partnership (GECIP) consists of groups or ‘domains’, overseen by the GECIP Board.

Each domain covers a different disease or topic in the project. The groups are responsible for interpreting the data to improve clinical care, and also undertake complementary research, including medical, computational and social research.

The GECIP Board oversees the operation of GECIP and includes representatives from GECIP funders and the GECIP domains. Up to three places on the GECIP Board are reserved for the representatives of the Participant Panel and they contribute and vote as any other member of the GECIP Board. The individual Participant Panel representatives are free to rotate attendance at the GECIP Board according to their availability.