Working with the ICR-CTSU

We work with researchers worldwide to develop our research and maximise use of our data.

Who we are

Our team of experienced statisticians, trial managers, data managers, clinical IT systems and administrative staff supports the full trial life cycle from initial discussions of trial concept, through design and development, day-to-day management, to analysis and reporting.

Who we work with

Patients and the public

We work in partnership with those affected by cancer to lead innovative, equitable scientifically-rich cancer trials, develop underlying trial methodology and, by maximising use of participants’ data, gain further understandings of mechanisms of action and markers of treatment sensitivity or resistance.

International researchers

We work together with clinicians and other researchers, including laboratory-based and data scientists, to help formulate and drive clinical research priorities.

We also collaborate with national and international collaborative groups and other trials units to support and conduct research worldwide.

We work with individual clinicians located across the UK and in close conjunction with the relevant NCRI Clinical Studies Groups to help formulate and drive national clinical research portfolios.

We also collaborate with national and international collaborative groups and trials units to conduct trials within the international framework.

Our team of experienced statisticians, trial managers, data managers, clinical IT systems and administrative staff supports the full trial life cycle from initial discussions of trial concept, through design and development, day-to-day management, to analysis and reporting.

Areas of expertise

ICR-CTSU staff have expertise in the design, central management and analysis of clinical trials, including the following:

  • Statistical design and sample size calculation
  • Protocol development
  • Preparation of funding applications
  • Design of case report forms
  • Development of specialist clinical trials IT systems
  • Central trial management and monitoring
  • Data and sample collection
  • Data management and monitoring
  • Quality assurance and regulatory affairs
  • Analysis and reporting

We are always interested in discussing new studies that would fit within our portfolio. For more information please take a look at the following documents and then get in touch with the ICR-CTSU team:

Data and sample sharing arrangements

We are committed to responsible sharing of clinical trial data and trial research samples with the wider research community to improve knowledge about cancer.

The availability of patient data and sample collections is vital for research into cancer. We oversee a large resource of patient data and linked patient samples generated from our clinical trials and recognise its potential to help address critical research questions beyond those in the original trial protocol.

We have a responsibility to ensure that clinical trial data and samples are shared within the terms of the consent with which they were collected and in accordance with relevant governance and legislation. We prioritise sharing for research projects of high scientific value and with due regard to the terms and conditions of the funders and sponsors of the original research.

Our data and sample access policy is framed around the importance of:

  • Protecting our study participants’ rights and confidentiality
  • Ensuring compliance with relevant legal and regulatory requirements
  • Prioritising access to ensure the optimal use of resources, especially depletable sample resources
  • Fostering high quality research and collaborations

You can find out more about how to make an access request and how this is reviewed using the links below:

Data and Sample Access policy  Data and Sample Access Request form

If you are interested in requesting access to ICR-CTSU data or samples please contact [email protected] for discussion with the relevant team.

Join the team

We are a multidisciplinary team of clinical trials professionals and applied methodologists and welcome applications from both experienced trialists and those early in their career.

Our comprehensive internal training programme, which supplements the ICR’s wider training opportunities, aims to equip our staff with the skills and knowledge they need for a rewarding career in clinical trials.

We also host PhD students, university industrial placement students, summer placement students and other short term placement opportunities.

Inclusivity and representation are important to us and the ICR has a range of forums to help celebrate and support diversity, including the Race, Ethnicity and Cultural Heritage Forum and LGBT+ Network. Having a diverse team also helps us to consider how to make our research as inclusive as possible.

For details of our current opportunities please visit the ICR’s vacancies page.

Current vacancies

Tessa Jowell Brain Cancer Mission: Clinical Fellowship in Neuro Oncology

  • Sutton
  • Clinical Studies
  • Salary Range: £43,923 - £63,152 per annum
  • Fixed term

The Tessa Jowell Fellowship The Tessa Jowell Fellowships, hosted in collaboration with Tessa Jowell Centres of Excellence (TJCE), are designed to support clinicians to address the needs of the future of neuro-oncology. The 12-month funded Fellowships aim to train highly skilled clinicians that are capable of appreciating the breadth of comprehensive brain tumour management and can integrate knowledge and experience in personalizing and optimising cancer care. The intention is for the Fellow to gain experience with the ultimate objective of leading high impact practice changing neuro-oncology clinical trials in the future as a Chief Investigator. This particular fellowship is for a dedicate Neuro-Oncology Clinical Fellow within the Drug Development Unit at the Institute of Cancer Research and The Royal Marsden. The Institute of Cancer Research The ICR is one of the world’s most influential cancer research institutes with an outstanding record of achievement dating back more than 100 years. The scientists at the ICR have contributed to identifying several cancer genes, discovered multiple practice changing cancer drugs and have developed precision therapies. Together with our hospital partner The Royal Marsden (RM) , we are rated in the top four centres for cancer research and treatment worldwide. The ICR was ranked first in the UK for its research in biological sciences in a combined assessment of research quality, impact and environment; and overall, second in the UK among all higher Education institutions in REF 2021 analysis. The Royal Marsden The Royal Marsden is recognised worldwide for the quality of it cancer services. The Trust’s strategic aim is to achieve excellence in cancer treatment and diagnosis, through partnership and collaboration. The prime purpose of the Trust is the provision of state of the art cancer services as well as enabling research into the development of improved methods of prevention, diagnosis and treatment of cancer. Its other main purpose is teaching and the dissemination of knowledge both nationally and internationally. The Drug Development Unit, The DDU within the ICR and Royal Marsden, is a dedicated Clinical Trials Unit, with bespoke facilities to conduct early phase clinical trials. The Unit, led by Professor Johann de Bono, comprises of clinicians, scientists, data and study management staff, and focuses on providing a seamless conduit between pre-clinical drug discovery, proof of principle Phase-1 clinical trials and tumour specific evaluation of novel agents. The Unit undertakes both industry-sponsored and investigator-initiated trials of new anti-cancer drugs. The Unit is rapidly expanding and provides an excellent opportunity for the post holder to develop a variety of skillsets. Summary of Role TJBCM Fellowships are for applicants who are near completion of training in clinical or medical oncology. Applicants will need to be able to demonstrate that they meet the range of skills and experience outlined in the person specification. The fellowship is focused on providing extensive clinical experience working with novel targeted therapies as well as experience in all aspects of Phase 1 trial conduct, over twelve months. Importance is placed on the longitudinal experience of managing brain tumours in these settings, in which clinical oncology trainees usually have approximately 4-months and medical oncology trainees have zero experience within a standard training programme. Fellows are further encouraged to gain experience and understanding of the multi-disciplinary approach to brain tumour management, with the opportunity to spend one day a week observing and learning from the various disciplines involved in brain tumour management. The objective of the Tessa Jowell Drug Development Unit Fellowship is to offer the opportunity for a medical oncology (or clinical oncology) trainee who wishes to gain specific experience in early clinical trials with a specific focus on neuro-oncology. The post provides: extensive clinical experience working with novel targeted therapies in oncology(clinics, ward work and consultant ward rounds) experience in all aspects of Phase 1 trial conduct from protocol development, trial setup, trial conduct in line with GCP, clinical and administrative management of trials, decision making on dose escalation, correlation of clinical and laboratory findings (pharmacokinetics, pharmacodynamics). The majority of the anti-cancer drugs being explored at often at a very early first in human stage and span a breath of immune-oncology, DNA damage-response therapies, targeted therapies as well as novel anti-cancer strategies. Opportunities to be involved in projects leading to publication of manuscripts, and trial presentation at national and international meetings. For suitable candidates, there is the option to develop grant applications and translational project proposals for higher degrees (MD/PhD). To apply for this post, please submit an online application including a supporting statement, detailing reasons why you are applying for the post and include your CV. We encourage all applicants to access the job pack attached for more detailed information regarding this role.

Postdoctoral Training Fellow - Bioinformatics

  • Sutton
  • Clinical Studies
  • £45,600
  • Fixed term

Professor Johann de Bono’s translational research team is seeking a talented Postdoctoral Training Fellow. The programme focuses on integrating multi-omic and clinical data, including single cell and spatial data as well as hyperplex immunocytochemical data, to help develop novel therapeutic strategies against cancer. For general information on Post Docs at The ICR can be found here. Key Requirements The successful candidate will be highly motivated and possess robust bioinformatic, scientific, and analytical skills, with a proactive approach to learning and applying new techniques, including artificial intelligence. Primary responsibilities will involve working with integrated datasets including clinical trial datasets comprising next-generation sequencing data and other applications relevant to the analysis of DNA and RNA sequencing, as well as protein assays. Familiarity with cancer genomics is desirable. The ICR has a workforce agreement stating that Postdoctoral Training Fellows can only be employed for up to 7 years as PDTF at the ICR, providing total postdoctoral experience (including previous employment at this level elsewhere) does not exceed 10 years Department/Directorate Information: Professor Johann de Bono is a world leader in anticancer drug development, biomarker studies, and prostate cancer care. His team conducts biomarker-driven clinical and translational research to accelerate the development of novel cancer therapies and improve understanding of cancer biology, drug sensitivity and resistance. His team has driven major advances in cancer care through early and late stage trials, and he has led pivotal phase III trials of several prostate cancer drugs including abiraterone, cabazitaxel, enzalutamide, lutetium PSMA and olaparib. His team consists of basic, translational and clinical scientists, and is embedded in a vibrant world-class research environment. We encourage all applicants to access the job pack attached for more detailed information regarding this role. For an informal discussion regarding the role, please contact Dr Wei Yuan via email on [email protected] Due to the high volumes of applications that we receive, we reserve the right to close the advert before the published closing date, once we have received a sufficient number of applications. Therefore, we advise that you to submit your application, as early as possible to avoid disappointment.

Training and development

Clinical research fellows and PhD students

We have a rolling programme of studentships with clinical fellows and PhD students embedded within the ICR-CTSU to gain applied knowledge of clinical trial development, conduct and reporting whilst working towards a PhD.

We have a number of PhD students working on a wide range of projects including refining methods for biostatistical analysis, assessing and enhancing equality diversity and inclusion and improving collection of patient reported outcomes.

Find out more about current PhD opportunities.

Clinical trial professional development

Our in-house staff training programme includes trial regulation and conduct training, specialist data management training and bitesize statistics workshops for non-statisticians. In addition to this our staff benefit from attending external career development training and events.

We run a regular series of research meetings at which we present our work and invite external speakers to discuss topics of interest to the wider ICR. Our staff can also access the wider programme of ICR seminars covering all of the work at the Institute, and benefit from the ICR training programme.

STEM outreach

We recognise the crucial importance of promoting the rewarding and varied career available in clinical trials to the next generation. We attend careers fairs at schools and universities and we are always looking for an opportunity to engage with students, particularly any which involve groups currently underrepresented in STEM careers. Contact us at [email protected] if you would like us to attend or speak at an event you are organising.

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Contact us

Get in touch with us for general enquiries and finding out more about our clinical trials.