Working life and benefits

The Clinical Trials and Statistics Unit at The Institute of Cancer Research (ICR-CTSU) is recruiting to its statistical team. We want to hear from you if you: • Like the challenge of analysing clinical trial datasets and want to become part of a statistical team that is dedicated to translating cutting-edge science into quality clinical trials that can transform cancer care • Want variety in your work and opportunities to apply and broaden your statistical knowledge across a number of therapeutic areas in oncology • Like to work as part of a multi-disciplinary research team with like-minded statisticians, clinical investigators, translational analysts, bioinformaticians, and trial managers. Applications are now open for a Trial Statistician/Senior Trial Statistician position to join our team of over 20 Statisticians. This post offers an excellent opportunity for an enthusiastic and well-motivated Statistician to work in a dynamic and supportive academic environment at one of the leading UK cancer trials units. Key Requirements The successful applicant will have a post-graduate qualification in statistics or an allied field (or a first degree in statistics along with practical experience in medical statistics). Additionally, they should demonstrate a solid understanding of clinical trials and experience in applying statistical methods to real-world data. Effective oral and written communication skills and enthusiasm for collaborating with researchers from different disciplines are essential. Department/Directorate Information ICR-CTSU manages an exciting portfolio of national and international phase II and III clinical trials and an expanding number of early phase I/II cancer trials. You will work as part of a multi-disciplinary team on the statistical development, oversight and analysis of a number of clinical trials within ICR-CTSU’s portfolio and the ICR/Royal Marsden Drug Development Unit’s early phase trials portfolio as well as on associated trials methodology research and translational biomarker research studies. We encourage all applicants to access the job pack attached for more detailed information regarding this role. 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 the probation period/key training and if the role allows. Flexible working options may be considered. For informal discussion about the Trial Statistician/Senior Trial Statistician post, please contact Lucy Kilburn (Principal Statistician), email: [email protected] For general queries about the recruitment process, please contact ICR-CTSU, email: [email protected].

Summary of Role We would like to appoint a Senior Trial Manager to be responsible for: • Day to day management of the trial(s) through set-up, recruitment and reporting; • Liaising with stakeholders and participating centres to promote the trial(s) and ensure successful recruitment and delivery; • Co-ordination of data management and biological sample collection activities. The post offers an excellent opportunity for an enthusiastic and well-motivated individual with clinical trial management experience to work in a dynamic and supportive academic environment in a dedicated cancer clinical trials unit. The successful applicant will be responsible for the central coordination of multicentre cancer trials. Key Requirements Applicants should hold a first degree or equivalent level qualification in biological science, social science or other relevant subject (including nursing and health care disciplines) or equivalent, relevant work experience and have a good understanding of the principles of GCP, data protection and research governance. Experience in clinical trial management is essential. We encourage all applicants to access the job pack attached for more detailed information regarding this role. Department/Directorate Information The Institute of Cancer Research is looking for a Senior Trial Manager to join the Cancer Research UK Clinical Trials & Statistics Unit (ICR-CTSU) at its Sutton site in Surrey. ICR-CTSU runs a diverse portfolio of national and international phase III multicentre randomised controlled trials, and phase II trials of targeted treatments with a focus on breast, urological and head and neck cancer treatments. Informal enquiries can be made by emailing [email protected].

Job Details The Cancer Research UK funded Clinical Trials and Statistics Unit at The Institute of Cancer Research (ICR-CTSU) seek an experienced and highly motivated Principal Statistician to join their team of over 20 statisticians. 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 on being part of a multi-disciplinary research team with like-minded statisticians. Are looking to develop your career within a dynamic and supportive academic environment at a leading cancer clinical trials unit. Key Requirements 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 have a post-graduate qualification in statistics. They should demonstrate a solid understanding of clinical trials and experience in applying statistical methods to real-world data. Familiarity with Bayesian statistics and early phase adaptive trials are highly desirable. Effective oral and written communication skills, as well as enthusiasm for collaborating with others from diverse disciplines, are essential. Department/Directorate Information ICR-CTSU manages an exciting portfolio of national and international phase II and III cancer clinical trials and an expanding number of phase I trials. You will contribute in shaping the development of methodological innovations and implementing efficient methods in new and ongoing trials, with a specific focus in early phase and adaptive trials. You will work as part of a multi-disciplinary team on trials methodology research and on the statistical development, oversight and analysis of a number of clinical trials within the ICR-CTSU’s Early Phase and Adaptive Trials portfolio in collaboration with external organisations and the ICR/Royal Marsden Drug Development Unit. In your supporting statement please summarise how your research/managerial experience fits with the role. We encourage all applicants to access the job pack attached for more detailed information regarding this role. 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 only if the role allows. Flexible working options may be considered. For informal discussion about the role, please contact Professor Christina Yap, email: [email protected] For general queries about the recruitment process, please contact ICR-CTSU, email: [email protected].

Summary of Role ICR’s Cancer Research UK Clinical Trials & Statistics Unit (ICR-CTSU) is offering a placement year training opportunity at its Sutton site in Surrey for an enthusiastic, adaptable, and quick learning individual, currently undertaking a life science undergraduate degree. This an exciting opportunity for students interested in a career within clinical trials to receive training within a clinical research setting. The successful applicant will work directly with the ICR-CTSU Clinical Trial & Data managers and Trial administrators to support the delivery of a diverse portfolio of phase II/III clinical trials, with a special emphasis in breast, urological and head and neck cancer treatments. You will receive full training in Good Clinical Practice and experience of working in accordance with UK clinical trials legislation. This will put you ahead of the competition when you graduate if you apply for a role in clinical trials either in academic research or in industry. You should be a life science student in your second year of study seeking a placement year opportunity in clinical trials. This post will be office based. When applying please provide a supporting statement; together with your CV and the names and addresses of two referees. Key Requirements The successful candidate must be studying for an undergraduate degree in life sciences. You should have a high level of computer literacy, a proven ability to use MS office packages and work accurately with attention to detail as well as good written and oral communication skills. You should be able to use electronic systems for recording and managing information and the ability to adhere to written procedures, work to agreed deadlines and work as part of a team. An interest in cancer research and the ability to work with confidential information is also essential. For full details of the requirements see the job description. Department/Directorate Information For information regarding the ICR-CTSU Team go to: https://www.icr.ac.uk/our-research/centres-and-collaborations/centres-at-the-icr/clinical-trials-and-statistics-unit 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 us via email at: [email protected]