Working in a Registered CTU
Working in an an academic or non-commercial CTU can offer you exciting opportunities that may not be available to you elsewhere. These range from publishing your research, presenting at national or international conferences, or teaching the next generation of researchers, as well as making a positive difference to patient and public health.
You can download some information on the different types of roles in CTUs here.
Below you can find some of the vacancies currently available across our 50 registered CTUs. You can also find vacancies on www.jobs.ac.uk.
If you are looking to work with a specific unit or in a particular area of the country then you might also like to visit the websites of individual CTUs. These can be identified via our CTU Finder.
We also occasionally share details of committee roles that may be of interest to colleagues across our Network. You can find details here.
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Analyst/Programmer – Oxford CTSU
Job title: Analyst/Programmer
Salary: £39,424 to £47,779 per annum (pro rata)
Contract type: Fixed term
Working pattern: Full time (part time considered)
Closing date: 9 July 2026 (12 noon)
About us
Oxford Population Health (Nuffield Department of Population Health) is home to world-renowned population health research groups and provides an excellent environment for multi-disciplinary research and teaching. The Clinical Trial Service Unit (CTSU) is a major international research institute within the NDPH, and is a world-leading centre for large-scale research into the causes, prevention and treatment of chronic diseases (such as cancer and cardiovascular and kidney disease).
About the role
We are seeking an Analyst/Programmer with skills to support and develop IT systems used to conduct large-scale clinical studies. The role involves the full application life cycle, including developing, refining and testing applications used to manage our studies.
About you
To be considered for the role, a BA, BSc or similar or equivalent experience in software development is required along with experience in a selection of the following: C++Builder, C/C++, Delphi or other similar languages. You will also have excellent communication skills with a positive attitude to acquiring new skills and taking on new responsibilities.
Further information
The position is full time (although part time considered) and fixed term for 2 years.
For a full role description, and to apply, please click here.
Data Manager – OCTO
Job title: Data Manager
Salary: £35,681 – £41,636 per annum (pro-rata)
Contract type: Fixed term for 2 years
Working pattern: Full time (80% worked over no fewer than 4 days will be considered)
Closing date: 13 July 2026 (12 noon)
About the role
We have an exciting opportunity for a Data Manager to join the Oncology Clinical Trials Office (OCTO). OCTO, part of the University of Oxford’s Department of Oncology, is a leader in early cancer detection, precision prevention, and therapy trials, delivering high-quality academic clinical research.
As a Data Manager, you will provide support and advice across clinical trials and studies requiring the capture, storage, management, review, and reporting of clinical research data. You will work closely with database programmers, trial management teams, investigators, statisticians, and external collaborators to develop appropriate data collection tools and documentation. You will contribute to monitoring the completeness, accuracy, consistency, and validity of trial data, ensuring that datasets specified for each trial meet the standards of quality expected with particular consideration of the requirements of GCP as well as the UK clinical trials and data protection legislation.
This post is based at the Oncology Clinical Trials Office (OCTO), Level 2, Cancer & Haematology Department, Churchill Hospital, Headington, Oxford, OX3 7LE and is offered on a full-time (80% worked over no fewer than 4 days will be considered), fixed-term basis for 2 years.
An early start date is essential for this role.
About you
You will hold a degree or equivalent qualification in a biomedical, scientific, statistical, or allied field, or have equivalent experience working in clinical trials/research studies. You will have experience of working in clinical trials/research studies with particular experience in handling clinical trial data (to include Clinical Trials of Investigational Medicinal Products (CTIMPs).
You will have knowledge and experience in developing, managing, and maintaining processes and systems for the collection of clinical trial data including entry, processing, validation, and be familiar with electronic data capture systems, ideally REDCap and/or OpenClinica.
You will be organised, analytical, and able to work independently, prioritise tasks, and communicate effectively with colleagues and collaborators.
Further information
If you would like to discuss this role, please contact Sarah Pearson at sarah.pearson@oncology.ox.ac.uk.
For a full role description, and to apply, please click here.
Research Group Leader – ICR-CTSU
Job title: Research Group Leader
Salary: £66,092 – £86,908 per annum
Contract type: Permanent
Working pattern: Full time
Closing date: Applications will be reviewed on receipt, and we reserve the right to close the application early should an appropriate candidate be found
The ICR-CTSU is a Cancer Research UK-funded, internationally recognised methodologist led clinical trials unit, providing cancer-focused clinical trial research expertise. We lead pioneering, efficient, high-quality, and impactful trials across the phases.
Our expertise ranges from experimental medicine early phase studies exploring biological efficacy to trials which may deliver widespread change to routine practice, underpinned by applied methodology to drive forward clinical trial innovation.
Role Summary
The Group Leader will lead a component of ICR-CTSU’s portfolio of clinical trials research. The post holder will join an existing faculty and seek to further develop and grow the portfolio in line with ICR-CTSU’s overall strategy; taking responsibility for a number of ongoing trials as well as the development of new trials. There will be the opportunity to develop and grow a team including the potential for a Postdoctoral Training Fellow and/ or a Trial Manager.
We seek an experienced statistician / biostatistician with a strong research interest in clinical trials methodology and a passion for direct involvement in the oversight and leadership of academic clinical trials. The successful candidate will work closely with the Director of ICR-CTSU to further enhance the Unit’s internationally recognised strength in clinical trial design, conduct and analysis.
The post holder will be expected to make a substantial independent intellectual contribution to clinical trials projects and be proactive in leading and contributing to broad initiatives that enhance the overall effectiveness of ICR-CTSU. The appointee will contribute to the overall scientific life of the ICR including the newly established ICR/Royal Marsden Hospital’s Centre for Trials and Population Data Science, by providing mentorship to more junior colleagues and acting as an academic leader.
We seek an individual who will work closely and collaboratively with other faculty/Group Leaders at the ICR and with international/national key opinion leaders to extend the breadth and depth of ICR-CTSU’s biologically rich clinical trials portfolio. In partnership with clinical opinion leaders, this individual will generate research funds to conduct and deliver clinical trials research at the international forefront. Presentation at national and international conferences, production of top-quality research outputs and substantial professional contribution to wider clinical trial network bodies are expected. Enthusiasm for team-based science in a collaborative interdisciplinary environment is essential.
The appointment will be based on track record and the ability and willingness to engage in team science. The successful appointee will have access to ICR’s successful PhD training programme and core facilities.
Further details
At ICR, academics are appointed as either Career Faculty- which is non-time limited with a competitive salary, or as Career Development Faculty – which is a six-year fixed term contract on the Career Development Faculty scale, starting at £66,092 in the first instance.
For an informal discussion regarding the role, please contact Professor Emma Hall (Emma.Hall@icr.ac.uk).
For a full role description, and to apply, please click here.
Clinical Trials Programme Manager – The ICR-CTSU
Job title: Clinical Trials Programme Manager
Salary: From £50,825 per annum (pro rata)
Contract type: Fixed term (for 2 years in the first instance)
Working pattern: Full time (or part time minimum of 60% FTE)
Closing date: 19 July 2026
About the role
The Institute of Cancer Research is looking for an experienced trialist to join the Cancer Research UK Clinical Trials & Statistics Unit (ICR-CTSU) as a Clinical Trials Programme Manager at its Sutton site in Surrey. ICR-CTSU runs a diverse portfolio of national and international phase III multi-centre randomised controlled trials, and phase II targeted treatment trials, with a special emphasis in breast, urological, lung and head and neck cancer treatments.
The post offers an excellent opportunity for an enthusiastic and well-motivated senior trial manager with extensive experience of setting up and running multi-centre trials to work in a dynamic and supportive academic environment. The successful candidate will join the ICR-CTSU Management Group and responsibilities will include:
* The strategic oversight of a defined programme of research within the ICR-CTSU portfolio;
* The development and initiation of new trials;
* Providing operational oversight of dedicated trials teams to ensure successful trial delivery.
About you
Applicants should hold a first degree or equivalent level qualification in life science or health related subject and have an in depth understanding of the UK Clinical Trials Regulations, principles of Good Clinical Practice, Data Protection, Research Governance and the Human Tissue Act. Experience/knowledge of laboratory quality systems and procedures is highly desirable. A proven track record in the planning, coordination and conduct of clinical trials within the NHS or academia, a CRO or a pharmaceutical company is essential.
Further information
This is an office-based role. Requests for hybrid working (splitting time between our Sutton site and home) may be considered following successful completion of key training and if the role allows. Flexible working options may be considered.
For an informal discussion regarding the role, please email ctsu@icr.ac.uk.
For a full role description, and to apply, please click here.
Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology – Sheffield CTRU
Job title: Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology
Salary: £71,566 to £75,915 per annum (pro rata)
Contract type: Permanent
Working pattern: Full time (part time at a minimum of 0.6 FTE will be considered)
Closing date: 30 June 2026
Are you an experienced clinical trials statistician with a passion for cancer research who enjoys working collaboratively to lead high-impact studies? We have an exciting opportunity for a Professor in Medical Statistics to be the Academic Lead for Clinical Trials in Oncology at the Sheffield Clinical Trials Research Unit (CTRU).
About the role
This role has been created following a prestigious multi-million-pound infrastructure grant. As the Academic Lead for Oncology Trials, you will provide senior oversight, leadership, and support for the development of a parallel stream of clinical trials in cancer within the CTRU.
Your work will have a direct impact on patient outcomes. You will lead the building of a sustainable pipeline of high-quality studies, ensuring that ambitious clinical ideas are translated into life-changing treatments.
From co-designing and overseeing complex oncology CTIMPs and navigating MHRA inspections to mentoring the next generation of triallists and clinical fellows, you will lead a portfolio that prioritises innovation and equity.
About you
We are seeking a senior statistician with a proven track record of leadership within an oncology setting. You will be a strategic collaborator capable of bridging the gap between ambitious clinical questions and rigorous methodological excellence.
The ideal candidate will:
* Hold a Post-graduate qualification and / or equivalent professional experience in Medical Statistics or a closely related discipline.
* Possess deep expertise in the design and analysis of Oncology CTIMPs, including an understanding of cancer-specific pharmacovigilance, UK regulatory frameworks, and MHRA requirements.
* Demonstrate a track record in Trial Development, with the ability to design efficient, high-impact studies—from early-phase dose-finding to large-scale Phase III trials.
* Show mastery of oncology-specific methodologies including but not limited to survival analysis and adaptive designs.
* Be a skilled communicator and grant-winner, capable of building strong relationships with Chief Investigators, funding bodies, and patient panels to secure major research investment.
Further information
For informal enquiries about this job contact Prof Matt Hammond, Director of the Sheffield Clinical Trials Research Unit: on matthew.hammond@sheffield.ac.uk.
For a full role description, and to apply, please click here.
No vacancies currently listed
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Please check back in a few days.
Quality Officer – Oxford CTSU
Job title: Quality Officer
Salary: £39,424 to £47,779 per annum (pro rata)
Contract type: Fixed term (for 2 years in the first instance)
Working pattern: Full time (part time considered)
Closing date: 29 July 2026 (12 noon)
Oxford Population Health (Nuffield Department of Population Health) contains world-renowned population health research groups and provides an excellent environment for multi-disciplinary research and teaching. The Clinical Trial Service Unit (CTSU) is a major international research institute within the NDPH, and is one of the world’s leading centres for research into chronic diseases, such as cancer and heart disease.
About the role
We are seeking a Quality Officer to work within our Clinical Trial Service Team to develop and maintain the Quality Management System, review risk assessments and monitoring plans and assisting with internal and external audits. This is an exciting opportunity to join our world-leading trials team and help to develop our Quality Assurance function within it.
About you
To be considered for this post you will have a university degree, knowledge of clinical trial governance and the regulatory requirements, including Guidelines for Good Clinical Practice (GCP), as well as an understanding of GDPR and the Data Protection Act 2000. You will also have a proactive approach to reviewing, updating and improving processes with excellent time management and communication skills.
Further information
The post is full time (part time considered) and fixed term 2 years. The closing date for applications is noon on 29 July 2026.
For a full role description, and to apply, please click here.
Medical Statistician – Leeds CTRU
Job title: Medical Statistician
Salary: £33,951 to £39,906 per annum
Contract type: Ongoing
Working pattern: Full time
Closing date: 5 July 2026
About us
The Clinical Trials Research Unit within the Leeds Institute of Clinical Trials Research (LICTR) is an international leader in the field of clinical trials. The Unit is one of the largest in the UK and conducts national and international randomised and early phase clinical trials in a variety of clinical fields. Our main aim is to develop and support novel and efficient trials to change clinical practice for the better. Our past results and current research have already helped to do this. Our results inform the academic development of this specialised field of clinical research on a national and international level. Particularly, we specialise in the development, optimisation and evaluation of complex interventions, complex phase III trials and efficient phase I/II trials, as well as adaptive designs, seamless phase II/III designs and biomarker driven designs.
About the role
You will join a large, well-established group of statisticians and will work on trials designed to answer questions of real importance that will contribute to improved care pathways and patient outcomes across a range of long-term health conditions of strategic importance to NHS, patients and social care.
You will have opportunities to research, apply and develop statistical methodology, together with general consulting and training of health professionals. You will be involved in a wide range of statistical activities, including designing, conducting, analysing and publicising clinical trials, preparing grant applications and presenting at national and international conferences.
You will work closely, interactively and collaboratively with a multidisciplinary project team, including statisticians, programmers, clinicians, health economists, health service researchers and trial managers.
This role will provide you with an excellent opportunity to develop your career and further broaden your expertise through methodological research within a supportive and stimulating environment; if applicable, you will also have the opportunity to register for a PhD.
About you
You will be a talented and dynamic individual with a postgraduate qualification, including a major statistical component, and an interest in evaluating novel treatments or interventions of pharmaceuticals, radiotherapy, surgery, medical devices or complex interventions.
We welcome applications from MSc students in the final year of their studies.
Further information
To explore the post further or for any queries you may have, please contact: Andrew Hall (Principal Statistician) Email: a.hall2@leeds.ac.uk.
For a full role description, and to apply, please click here.
Trial Manager – NPEU
Job title: Trial Manager
Salary: £39,424 to £47,779 per annum
Contract type: Fixed term for 2 years in the first instance
Working pattern: Full time preferred (other part time working arrangements may also be considered)
Closing date: 1 July 2026 (12:00)
The National Perinatal Epidemiology Unit, Clinical Trials Unit (NPEU CTU) are looking for an enthusiastic Trial Manager to join our team to provide project management for randomised controlled trials on the NPEU CTU portfolio. This is a great opportunity to join a friendly, supportive team with scope to contribute to wider development work of the Clinical Trials Unit.
About the role
The postholder will be based within the Nuffield Department of Women’s and Reproductive Health (NDWRH) which contains world-renowned health research groups and provides an excellent environment for multi-disciplinary research and teaching.
The NPEU is an internationally recognised, multi-disciplinary research unit based within the NDWRH at the University of Oxford, Radcliffe Observatory Quarter, Oxford. The unit undertakes research about pregnancy, childbirth and new-born babies.
As Trial Manager you will be the central administrative contact at the Coordinating Centre maintaining effective and efficient systems to ensure the trials are delivered according to milestones. You will co-ordinate the design, implementation and running of the clinical trials across participating hospital sites in the UK, ensuring timely data collection and Good Clinical Practice (GCP) compliance, and ensure they comply with NPEU CTU Standard Operating Procedures.
About you
To be considered for this role you will have a degree in a biomedical or associated subject, or other relevant qualification or proven experience in clinical research. You will have line management experience, as well as an understanding of clinical research methodology, good clinical practice and knowledge of all UK regulations for clinical trials, GDPR and the research governance framework. Proven administrative, data and project management skills and excellent organisational skills and the ability to prioritise your workload are also essential for this position.
Further information
The position is fixed term for 2 years in the first instance. Full time or a 50% job share are preferred; other part time working arrangements may also be considered.
For informal queries about the position, please contact Christina Cole (christina.cole@npeu.ox.ac.uk).
For a full role description, and to apply, please click here.
Clinical Trials Assistant – LSHTM CTU
Job title: Clinical Trials Assistant
Salary: £30,231 to £33,925 per annum
Contract type: Fixed term (for 12 months in the first instance)
Working pattern: Full time
Closing date: 13 July 2026
About the role
The London School of Hygiene & Tropical Medicine (LSHTM) is one of the world’s leading public health universities. Our mission is to improve health and health equity in the UK and worldwide; working in partnership to achieve excellence in public and global health research, education and translation of knowledge into policy and practice.
We are based within the Clinical Trials Unit at LSHTM, and work collaboratively with health professionals world-wide to conduct large multi-centre clinical trials aimed at improving patient outcomes in life threatening emergencies. We have an international reputation for practice changing clinical trials, including the CRASH-2 trial (20,000 patients with traumatic bleeding) which identified tranexamic acid as a lifesaving treatment for trauma victims and the WOMAN trial (20,000 women with postpartum bleeding) that showed that tranexamic acid also reduces deaths from bleeding after birth.
We are seeking to appoint an enthusiastic and innovative Clinical Trials Assistant. The successful candidate will support the Trial Manager and play a key role in the day-to-day Trial Management aspects of clinical trials being conducted by the CTU. The role will support some of the administrative aspects of trials. Ensuring professional and courteous service to trial collaborators, delivery in a reliable and compliant manner, in accordance with clinical trials regulations and ethical requirements.
About you
The post-holder must have an undergraduate degree in a relevant subject or equivalent relevant experience and experience working in research/regulated clinical trials. Further particulars are included in the job description.
Further information
The post is full-time 35 hours per week, 1.0 FTE and fixed-term for 12 months with potential for extension subject to funding. The post is funded by Unitaid and available immediately.
For a full role description, and to apply, please click here.
Clinical Trial Manager – Primary Care CTU
Job title: Clinical Trial Manager
Salary: £39,424 to £47,779 per annum (pro rata)
Contract type: Fixed term (for 2 years in the first instance)
Working pattern: Full time (part time may be considered)
Closing date: 22 July 2026 (12 noon)
Applications are invited for a Clinical Trial Manager, to work within the NDPCHS Primary Care Clinical Trials Unit (PC-CTU) led by Prof Chris Butler and Prof Ly-Mee Yu. Our clinical trials cover the broad range of issues that you might expect to address in the community, including cardiovascular and metabolic disease, cancer, infectious diseases and childhood illnesses, mental health and wellbeing, obesity, poor diet and smoking.
The PC-CTU offers a friendly and supportive team working environment and the opportunity to receiving training to further a career within trial management. We are currently recruiting for at least one Trial Manager post to lead on one trial in the unit, this may be a Clinical Trial of Investigational Medicinal Product (CTIMP).
About the role
Integrated within a busy, multidisciplinary UK Registered clinical trials unit, the successful applicant will work closely with the study Senior Trial Manager, as part of the trial management team and closely with other functions within the unit such as data, IT and statistics.
Responsibilities will include all key tasks within the lifecycle of the trial and line management either within the study itself or within the trial management group.
About you
The successful applicant will lead on one of the studies currently in set-up in the clinical trials unit, developing trial essential documents, gaining relevant regulatory approvals, conducting site initiation visits, managing recruitment and study logistics, contributing to data analysis and oversight committees.
You will hold a good first degree, or have equivalent experience in a research environment, and have detailed knowledge of a full life-cycle of study management. You will have strong computer literacy skills, be able to work well in a team, in a busy environment and have the ability to effectively prioritise tasks.
Further information
You will be based in the Gibson Building, Nuffield Department of Primary Care Health Sciences, Radcliffe Primary Care Building, Woodstock Road, Oxford, OX2 6GG, as your normal place of work but you may be able to agree a pattern of regular remote working with your line manager.
The trials we are recruiting for will be discussed during the interview process but if you would like to discuss these roles beforehand, please contact Jared Robinson, Senior Trial Manager: jared.robinson@phc.ox.ac.uk
For a full role description, and to apply, please click here.
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