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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Senior Data Manager – ERM, OCTRU
Job title: Senior Data Manager
Salary: £39,424-£43,984 per annum
Contract type:
Working pattern:
Closing date: 22 May 2026 (12 noon)
About the role
We have an exciting and unique opportunity for a Senior Data Manager to lead data management activities and provide data management expertise to the clinical trials managed by the Experimental Medicine and Rheumatology (EMR) trials group. In this role you will oversee the data related aspects of all EMR trials throughout the whole trial lifecycle ensuring they meet the required standards in a compliant and efficient manner.
You will work as part of multi-disciplinary teams with the Chief Investigators, Trial Management Team, Database Programmers, Statisticians and others as required to design case report forms (CRFs) and associated data matrices to capture the trial data, and to design, build (where required), test and maintain trial specific clinical databases, and other databases or systems required.
You will use your expertise to lead on the development of data related documents such data management plans, contribute to trial protocols, and provide training to the group.
About you
You will hold a Bachelor’s degree in IT or life sciences (or hold equivalent experience) together with proven experience in clinical research data management including the use of electronic data capture systems. You will have a working knowledge of good data management principles and Good Clinical Practice (GCP) requirements in the UK as well as proven experience in the design, use, maintenance and interrogation of relational databases. Additionally you will have a working knowledge of the clinical trial lifecycle with experience of UK clinical research structures, regulatory, ethical, and governance requirements and systems, including of the data protection regulations and the need for confidentiality.
Further information
Interviews will take place during week commencing 8th June 2026 and will be online/in person.
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.
Senior Project Manager (Senior Trial Coordinator) – CRUK & UCL CTC
Job title: Senior Project Manager (Senior Trial Coordinator)
Salary: £54,931– £64,644 per annum
Contract type: Open-ended, funded for 1 year in the first instance
Working pattern: Full time
Closing date: 22 May 2026 (23:59)
About the role
This post is in the Advanced Therapies group, which oversees one of the most comprehensive ATMP portfolios in Europe, primarily focused on Phase I, first in human, CAR T-cell trials.
We are looking to appoint a Senior Project Manager (SPM) who will be responsible for managing a portfolio of trials; ensuring that they are conducted according to the protocol, GCP and relevant regulations, and according to planned timelines.
The SPM has line management responsibility for Trial Managers (TM) and Data Managers (DM) and is expected to ensure that all members of their team are appropriately trained, supported and empowered to carry out their roles effectively. The SPM also works closely with the Senior Management Team to develop new trials, deal with issues in ongoing trials, prioritise and manage the workload of the team, and to continuously assess the working practices of the team to inform changes to improve communication, efficiency and quality.
About you
This is a high-level post, and candidates must already have acquired considerable experience in conducting and managing several clinical interventional trials, including developing a project plan, developing or amending protocols, case report forms and other trial-related documents, site set-up, monitoring trial progress, and how databases are prepared for analysis and trial close down.
They will also have experience of conducting CTIMPs with supplied IMP, costing clinical trials, handling/understanding agreements and contracts and supervising staff.
The majority of studies at the CTC involve evaluating investigational medicinal products, therefore the post-holder would also need to have sufficient knowledge and experience in these particular studies.
A knowledge of cancer and an understanding of the ethical issues involved in clinical research are also essential.
Further information
The CTC offers hybrid working with staff being able to work between the office and home – with a minimum of 60% FTE office attendance required.
If you have any queries about the role or application process, please contact ctc.hr@ucl.ac.uk
For full role description, and to apply, please click here.
Head of Clinical Trial Operations – Liverpool CTC
Job title: Head of Clinical Trial Operations
Salary: £61,759 to £75,917 per annum
Contract type: Permanent
Working pattern: Full time
Closing date: 1 June2026
Join a World-Class Academic Trials Unit.
Are you a strategic leader with a passion for clinical research? The Liverpool Clinical Trials Centre (LCTC), within the University of Liverpool’s Faculty of Health and Life Sciences, is seeking a Head of Clinical Trial Operations to lead on all aspects of operational activity.
As a key member of the LCTC leadership team, you’ll drive operational excellence, strategic growth, and stakeholder engagement across a diverse portfolio of clinical trials—from first-in-human studies to large-scale randomized trials. You’ll collaborate closely with the LCTC Director to align operations with institutional goals and research priorities.
We’re looking for someone with: Proven leadership in clinical trial operations with a background in trial management or quality assurance; a deep understanding of UK clinical research regulations and funding landscape; strong strategic planning and project management skills; excellent communication, negotiation, and analytical abilities.
For an informal discussion about the role, please email lctcadmin@liverpool.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
Contract type: Permanent
Working pattern: Full time
Closing date: 2 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.
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 Sheffield CTRU is a vibrant, multidisciplinary unit within the School of Medicine and Population Health. We are a UKCRC-registered unit with a reputation for excellence in the design and delivery of complex, randomised controlled trials. This is a unique opportunity to join a team that is expanding its horizons into specialist cancer research, backed by significant long-term funding. You will work in a supportive environment that values methodological innovation and professional development.
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.
No vacancies currently listed
Please check back in a few days.
Senior Medical Statistician – Primary Care CTU
Job title: Senior Medical Statistician
Salary: £49,119 to £58,265 per annum
Contract type: Fixed term (3 years in the first instance)
Working pattern: Full time
Closing date: 5 June 2026 (12 noon)
About the role
Applications are invited for a Senior Medical Statistician, to join the Primary Care Clinical Trials Unit (PC-CTU) trial statistics team.
The successful applicant will be expected to contribute to all statistical aspects of clinical trial activities within the CTU and outside the PC-CTU. In addition, the successful applicant will play a key role as Lead Advisor supporting researchers within the NIHR Research Support Service University of Southampton and Partners.
About you
You will hold a Postgraduate degree in statistics supported by a publication record and experience in working on Clinical Trials as Senior Medical Statistician.
Further information
For further information or discuss the post please contact Dr Milensu Shanyinde milensu.shanyinde@phc.ox.ac.uk.
For a full role description, and to apply, please click here.
Medical Statistician x 2 – Primary Care CTU
Job title: Medical Statistician x 2
Salary: £49,119 to £58,265 per annum
Contract type: Fixed term
Working pattern: Full time or part time
Closing date: 10 June 2026 (12 noon)
About the roles
Applications are invited for two Medical Statisticians, to join the Primary Care Clinical Trials Unit (PC-CTU) trial statistics team.
The successful applicants will be expected to contribute to all statistical aspects of clinical trial activities within the PC-CTU and outside the PC-CTU.
About you
You will hold a Postgraduate degree in statistics supported by a publication record.
Further information
There are two positions available. The first position is offered for two years in the first instance. The second position is available for two years or until 30 September 2028, whichever is sooner. We welcome applications from candidates interested in either full-time or part-time work.
For further information or discuss the post please contact Dr Milensu Shanyinde milensu.shanyinde@phc.ox.ac.uk.
For a full role description, and to apply, please click here.
Senior Statistician/Principal Statistician – The ICR-CTSU
Job title: Senior Statistician/Principal Statistician
Salary: Senior Statistician: £47,634 – £52,324 / Principal Statistician: £49,970 – £63,120 per annum (pro rata)
Contract type: Fixed term for two years
Working pattern: Full time (35 hours per week) / part time (minimum 60% FTE) will be considered
Closing date: 14 June 2026
About the role
The Cancer Research UK funded Clinical Trials and Statistics Unit at The Institute of Cancer Research (ICR-CTSU) seek an experienced and highly motivated statistician to join our team of over 20 statisticians and methodologists. This position will be appointed at either Senior Statistician or Principal Statistician level, depending on the successful candidate’s experience and qualifications.
We want to hear from you if you:
~ Enjoy the challenge of researching, developing and implementing efficient trial methodology, and designing efficient clinical trials that will make a difference in patients’ lives
~ Seek variety in your work and opportunities to apply your statistical knowledge across multiple therapeutic areas in oncology.
~ Thrive as part of a multi-disciplinary research team alongside like-minded statisticians and methodologists.
~ Are looking to develop your career within a dynamic and supportive academic environment at a leading cancer clinical trials unit.
About you
The successful applicant will be an experienced and highly motivated medical statistician interested in researching new statistical methods and applying their statistical knowledge to the design and analysis of patient-centred clinical trials. They will hold a post-graduate qualification in statistics and demonstrate a solid understanding of clinical trials, with experience in applying statistical methods to real-world data. Familiarity with Bayesian statistics and early phase adaptive trials is highly desirable. Strong oral and written communication skills, and enthusiasm for collaborating across diverse disciplines, are essential.
Further information
For an informal discussion about the role please contact Professor Christina Yap, email: Christina.Yap@icr.ac.uk.
For a full role description, and to apply, please click here.
Clinical Trial Manager (Site Engagement) – Warwick CTU
Job title: Clinical Trial Manager (Site Engagement)
Salary: £35,608 to £46,049 per annum (pro rata)
Contract type: Fixed term (12 months)
Working pattern: Part time (29.2 hours per week (0.8 FTE))
Closing date: 24 May 2026 (23:55)
Are you passionate about clinical trials and known for being a highly organised, proactive and a supportive team manager? If so, then you could be a great fit for Warwick Clinical Trials Unit (Warwick CTU).
About the role
We’re offering an exciting opportunity for a motivated and experienced Clinical Trial Manager to join our dynamic team. You’ll play a pivotal role in delivering high-quality trial management and leadership for an important ongoing study within our Cancer portfolio. Every trial we conduct is designed to improve patient outcomes and answer research questions that improve people’s lives.
The position is based in the ATNEC trial team, which is investigating axillary management in T1-3N1M0 breast cancer patients with needle biopsy proven nodal metastases at presentation after neoadjuvant chemotherapy.
As the Clinical Trial Manager (Site Engagement) for the ATNEC trial, you’ll be a key member of the trial team, with a focus on:
~ Leading on the day-to-day management of the ATNEC trial.
~ Taking responsibility for active engagement with sites, identifying barriers to recruitment and helping the sites to overcome these. This will include travel to sites.
~ Overseeing and implementation of key trial processes, including the supervision of other members of the trial team.
~ Confidently presenting information about the trial at meetings and producing accurate progress reports.
~ Fostering relationships with the site staff, collaborators and trial team.
~ Ensure the successful delivery of the study.
About you
You will need to have significant recent experience of managing clinical trials and with the knowledge of the regulatory environment, excellent project management and strong interpersonal skills, and be educated to degree level or equivalent.
You will have experience of working successfully with sites to recruit to target.
You will also need strong communication skills to work effectively with a wide range of stakeholders, including research site staff, trial participants, and oversight committee members. A keen eye for detail is essential, particularly when preparing, reviewing, and quality-checking trial documentation and processes.
Further information
For informal queries about the role, please contact Dalbir Kaur (Senior Project Manager) at Dalbir.kaur@warwick.ac.uk.
For a full role description, and to apply, please click here.
Clinical Trial Manager – Comprehensive CTU
Job title: Clinical Trial Manager
Salary: £43,981 to £52,586 per annum
Contract type: Fixed term
Working pattern: Full time
Closing date: 29 May 2026
About us
The Comprehensive Clinical Trials Unit is a specialist unit set up within the Institute of Clinical Trials and Methodology with a specific remit to design, conduct, analyse and publish clinical trials and other well-designed studies led by UCL Chief Investigators.
About the role
We are seeking an experienced Clinical Trial Manager to take responsibility for the day-to-day management and delivery of a First in Human Clinical Trial of an Investigational Medicinal Product (CTIMP). The post holder will work closely with Chief Investigators, sponsors, participating trial locations, and external partners to ensure the trial is conducted in full compliance with Good Clinical Practice (GCP), regulatory requirements, and the approved protocol.
You will play a pivotal role in the set-up and conduct of the trial at UCL Comprehensive Clinical Trials Unit (CCTU), ensuring effective coordination of study activities and delivery against agreed timelines. The role requires a strong focus on quality, governance, and risk management.
About you
We are looking for someone who can demonstrate:
~ Proven experience working as a Clinical Trial Manager on Clinical Trials of Investigational Medicinal Products (CTIMPs)
~ In-depth working knowledge of ICH GCP, UK clinical trial regulations, European Clinical Trials legislation, and the Department of Health Research Governance Framework
~ Demonstrable experience managing multi-centre clinical trials within the NHS, academic, or sponsor environment
~ Experience conducting on-site monitoring visits, including site initiation and routine monitoring
~ Excellent organisational and time-management skills, with the ability to manage multiple priorities and complex stakeholder relationships simultaneously
~ Strong written and verbal communication skills, with confidence in working collaboratively with Chief Investigators, site staff, and external vendors
~ Willingness and ability to travel across trial locations in the UK and Ireland
Further information
Please note that this role requires regular travel to trial sites across UK and Republic of Ireland, therefore please ensure that you have the necessary RTW documentation to undertake unrestricted travel to Republic of Ireland.
The role is available full time until 31 August 2027 and is based in Holborn, London
Interviews will be held in person on 17th June 2026 at 90 High Holborn.
For a full role description, and to apply, please click here.Please check back in a few days.
Senior Trials Manager – Southampton CTU
Job title: Senior Trials Manager
Salary: £46,049 to £58,225 per annum
Contract type: Fixed term (24 months)
Working pattern: Full time
Closing date: 2 June 2026
An exciting opportunity for someone with previous clinical trials experience to join the Southampton Clinical Trials Unit (SCTU), within the University of Southampton, in an important role as Senior Trials Manager (STM) within the Early Diagnosis and Translational Group.
About us
SCTU is a leading UK academic CTU located within the state-of-the-art Centre for Cancer Immunology building at Southampton General Hospital. Southampton Clinical Trials Unit (SCTU) | University of Southampton.
SCTU is a UKCRC registered CTU and is core-funded by Cancer Research UK (CRUK) together with funding from the National Institute for Health and Care Research (NIHR) via the Biomedical Research Centre (BRC) and Research Support Service (RSS).
SCTU has expertise in the design, conduct and publication of clinical trials and other well-designed studies from first-in-human phase I to practice changing phase III trials to large early diagnosis observational studies with rich translational data. Managing a growing portfolio (75% cancer, 25% non-cancer) that covers the complete spectrum of clinical practice, from primary care through to tertiary referral medicine, including pan-cancer experimental therapeutics, surgery, radiotherapy and early diagnosis. Undertaking multi-centre early and late phase clinical trials, we work nationally and internationally to create the evidence for patient benefit that will directly influence routine clinical practice in the NHS and overseas.
As part of the CRUK and NIHR infrastructure we have close working relationships with our partners, including the Southampton Experimental Cancer Research Centre, NIHR BRC & RSS, University Hospital Southampton, the Centre for Cancer Immunology discovery community and CRUK Centres and Institutes across the UK, with an increasing number of international collaborations.
About the role
The Senior Trials Manager will lead the relevant portfolio team to ensure effective delivery of the overall strategy and delivery priorities for SCTU. This will include resource management, oversight of financial management, new trial development, grant applications, and the ability to anticipate and consider potential issues or opportunities which could affect delivery and growth of the relevant portfolio.
About you
The appointed person must have proven experience of running clinical trials, with a focus on multistakeholder studies collecting patient samples for analysis, and including new trial development.
Further information
For informal queries please contact Nicole Keyworth, Portfolio Lead, on n.e.keyworth@soton.ac.uk.
For a full role description, and to apply, please click here.
Clinical Trial Manager (Multiple Positions) – Nottingham CTU
Job title: Clinical Trial Manager (Multiple Positions)
Salary: £35,608 to £47,389 per annum
Contract type: Fixed term
Working pattern: Full time (part time (min. 29 hours per week) considered)
Closing date: 12 June 2026
These posts are an exciting opportunity to join the Nottingham Clinical Trials Unit (NCTU) based on the leafy University of Nottingham campus. The unit designs and conducts high quality national and international multicentre trials across a range of health topics collaborating with clinicians and academics within the University and local NHS trust.
About the role
The unit is seeking to recruit experienced Clinical Trial Managers to work within our multidisciplinary team to ensure successful delivery of trials. They will work closely with the Chief Investigator, other researchers and clinicians to ensure efficient and successful completion of the trial. The post holder will also be responsible for supervising the activities of other members of the research team.
About you
Candidates should have a degree or equivalent qualification in a relevant subject, or significant experience as a clinical trial manager/coordinator, along with a track record of successful project management of clinical research. They should have experience of working within multidisciplinary teams with significant skills in understanding and applying knowledge to address complex problems and challenges.
Further information
These are full-time posts (36.25 hours per week) preferably; however, applications are invited from candidates wishing to work part-time (minimum 29 hours per week). Please indicate on your application if you wish to be considered for a role on a part-time basis. The roles will be offered on a fixed term contract until the 30th of June 2028. There may be the opportunity for an extension, but this would be dependent upon circumstances at the time.
Informal enquiries may be addressed to: Hugh.Jarrett@nottingham.ac.uk.
For a full role description, and to apply, please click here.
Clinical Trials Monitor – Pragmatic CTU
Clinical Trials Monitor – Pragmatic CTU
Job title: Clinical Trials Monitor
Salary: £40,015 to £46,618 per annum
Contract type: Fixed term
Working pattern: Full time
Closing date: 18 May 2026
About the Role
We are looking for a Quality Assurance Monitor to join a dynamic clinical trials unit supporting high quality clinical trials in primary care, psychiatry, women’s health, surgery and beyond. The Pragmatic Clinical Trials Unit (PCTU) is located in the Centre for Evaluation and Methods and linked with the Unit for Social and Community Psychiatry based in Newham.
You will work with the Quality Assurance team and the ChariotMS Trial Manager. You will be responsible for working alongside one other monitor in overseeing the unit’s regulated studies, primarily the ChariotMS study.
ChariotMS is a multi-centre, randomised, double-blind, placebo-controlled, phase IIb trial. The aim of the trial is to test oral cladribine (Mavenclad®) compared to placebo for safety, efficacy, and cost-effectiveness and to advance mechanistic understanding in people with advanced Multiple Sclerosis (MS). ChariotMS is the first ever disease modifying treatment (DMT) trial focussing on people with MS at this stage of disability.
About you
The successful candidate will have experience in monitoring research studies, writing up detailed, clear reports and escalating findings appropriately. They will have a good knowledge of Good Clinical Practice, Data Protection guidelines and Clinical Trials Regulations.
Further information
For a full role description, and to apply, please click here.
Clinical Trials Monitor – Imperial CTU
Job title: Clinical Trials Monitor
Salary: £46,614 – £56,345 per annum
Contract type: Fixed term
Working pattern: Full time
Closing date: 27 May 2026
About the role
We are looking for a Clinical Trials Monitor to join the UKCRC registered Imperial Clinical Trials Unit (ICTU) team, to be responsible for clinical trial monitoring activities for two innovative real-world data randomised controlled trials, including a CTIMP.
The COLLABORATE Trial is a UK‑wide adaptive study assessing the effectiveness and safety of commonly used enteral feeds in reducing necrotising enterocolitis, mortality and cognitive impairment in extremely preterm infants.
The PATH Trial will evaluate whether personalised antibiotic prescribing can improve survival in hospitalised sepsis patients while addressing antimicrobial resistance.
You will work closely with the Trial Managers, site teams, and clinical staff to ensure the trials are conducted in accordance with Good Clinical Practice (GCP) and regulatory requirements.
What you would be doing
You will be responsible for monitoring activities at investigator sites, including feasibility, initiation, enrolment and follow-up, close-out and archiving, with guidance from the Trial Managers.
You will:
~ Conduct on-site and central monitoring to verify source data and ensure compliance.
~ Perform Source Data Verification (SDV) and oversee site performance.
~ Perform Site Initiation Visits (SIVs) and Close-Out Visits (COVs).
~ Prepare monitoring reports and maintain regular site communication.
~ Monitor Investigational Medicinal Product (IMP) accountability.
~ Maintain the Trial Master File (TMF) and distribute Investigator Site Files (ISFs).
The role requires travel to investigator sites across the UK, with occasional overnight stays.
What we are looking for
~ Science degree or equivalent.
~ Monitoring experience, ideally for CTIMPs.
~ Experience conducting SIVs, monitoring visits, COVs, and performing SDV.
~ Knowledge of ICH-GCP and UK Clinical Trials regulations.
~ Strong communication, organisational skills, and attention to detail.
~ Willingness to travel and work flexibly.
Further information
The Imperial Clinical Trials Unit (ICTU) is a UKCRC-registered unit committed to excellence in clinical trial design, conduct, and dissemination. We deliver health benefits through high-quality research in a dynamic and supportive environment.
Fixed-term, full-time for 18 months with potential to extend subject to funding.
If you require further details, please contact: Hanna Box – h.box@imperial.ac.uk.
For a full role description, and to apply, please click here.
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PPI Specialist Member – CTU Network Executive Group
The UKCRC Registered Clinical Trials Unit (CTU) Network is seeking a highly experienced public contributor with expertise in clinical trials to contribute to the strategic work of its Executive Group.
The successful candidate will have a wealth of experience, knowledge, and acumen within the field of non-commercial/academic clinical trials research, demonstrate an excellent understanding of best practice as well as current drivers for change.
As the collective voice of non-commercial and academic clinical trials units, the Network plays an important role in engaging with Government, funders, regulators, and patients to improve and strengthen clinical research in the UK. The Network is seen internationally as an exemplar for the development of national clinical trials support. It was established in 2007, and its members are committed to setting and sharing good practice and improving standards in clinical trials.
The CTU Network is funded by its members, and major funders have representation on the Executive Group, this includes; Cancer Research UK, NIHR, Arthritis UK, Chief Scientist Office Scotland, and Health and Social Care Research Wales.
The deadline for applications is 6pm on 29 May 2026.
Download the applicant information pack here.
