SENIOR STATISTICIAN (BAND 7) / STATISTICIAN (BAND 6) DEPENDING ON EXPERIENCE.
An exciting opportunity has opened to join the Research Data & Statistics Unit (RDSU) as Senior Statistician or Statistician within The Royal Marsden NHS Foundation Trust.
Together with academic partner, Institute of Cancer Research (ICR), we are the largest cancer centre in Europe and the only National Institute of Health Research (NIHR) Biomedical Research Centre (BRC) specialising in cancer. The Royal Marsden Clinical Trials Unit (RMCTU) has full accreditation from UK Clinical Research Collaboration (UKCRC) Registered Clinical Trials Units Network, and statisticians within our team link to the NIHR statistics group.
As a team we work together to support all our staff to identify and work towards their individual development goals, and to recognise and value their own and others contributions towards the wider impact of RM as a whole.
* A post-graduate qualification in medical statistics is required, or equivalent experience.
* For the senior role, extensive experience in clinical trials and/or expertise in complex trial methodology is desirable.
Vacancies are full-time, initially for two years, based in Sutton and/or Chelsea, with possibility of hybrid working.
For further information please contact Karen Thomas (karen.thomas@rmh.nhs.uk)
Main duties of the job
The post holder will be part of the Research Data and Statistics Unit (RDSU), which provides expert support and advice relating to the full range of statistical and analytical aspects of the Trust's portfolio of sponsored clinical research studies.. The focus of the role is involvement in all aspects of study methodology, protocol development, eCRFdesign, data handling, statistical analysis, and publication of results. The post holder will support the statistical requirements of the Royal Marsden Clinical Trials Unit (RMCTU), which is a registered UKCRC trials unit. Band 7 post holders may be expected to have management responsibilities of junior statisticians within the team, which would involve ensuring they are trained to a competent level and have a development plan in place.
About us
The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals - one in Chelsea, London, and one in Sutton, Surrey - as well as a Medical Daycare Unit in Kingston Hospital.
At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.
At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements.
Job responsibilities
For further information on this role, please see the attached detailed Job Description and Person Specification:
* To maintain knowledge of global Good Clinical Practice guidelines (ICH GCP E6 (R3)), and ensure all work is carried out in compliance with relevant legislation (the MHRA Medicines for Human Use (Clinical Trials) (Amendment) Regulations 2025 for UK studies, and EU Clinical Trials Regulation for EU studies).
* To gain a good knowledge of the clinical features, management and treatment of the disease being studied, and to keep updated of any developments in the area.
* To liaise with, advise and educate clinicians on the statistical design and analysis aspects of clinical trials and research studies.
* To contribute to high quality grant applications, as required.
* To liaise with and support data managers and trial coordinators to ensure data quality.
Person Specification
Education/Qualifications
* Good honours degree or equivalent in a subject with a statistical component
* Higher qualification in statistics or appropriate experience in applied statistics, preferably in the role of medical statistician
Experience
* Experience in contributing to the statistical design of clinical trials
* Experience of carrying out survival analysis and the application of other relevant statistical techniques.
* Experience of presenting complex statistical information so that it is understandable to users without statistical knowledge
* Awareness of research governance issues in clinical trials.
* Evidence of publications in peer reviewed journals
* Evidence of collaboration on successful grant applications for clinical trial funding
* Expertise in complex trial methodology including but not limited to platform designs, adaptive trials, Bayesian methodology and research for rare diseases
* Experience of managing staff
Skills Abilities/knowledge
* Strong analytical and problem-solving skills, including the ability to select an appropriate methodology when analysing data
* Good working knowledge of STATA or similar statistical analysis packages
* Excellent statistical analysis skills
* Report writing and written presentation skills
* Good knowledge of the disease process and treatment of cancer
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
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