Research Nurse | The Royal Marsden NHS Foundation Trust
| Posting date: | 27 April 2026 |
|---|---|
| Salary: | Not specified |
| Additional salary information: | £45,953 - £54,254 per annum |
| Hours: | Full time |
| Closing date: | 27 May 2026 |
| Location: | Sutton, SM2 5PT |
| Company: | The Royal Marsden NHS Foundation Trust |
| Job type: | Permanent |
| Job reference: | 7955008/282-CR1441 |
Summary
Are you an experienced research nurse looking to make a real impact in oncology? Join our prostate research team at the West Wing Clinical Research Centre as a Band 6 Research Nurse. You will lead patient care across an expanding portfolio of clinical trials, from study set-up to treatment delivery and follow-up. This is a unique opportunity to work in a dynamic, supportive team, contribute to cutting-edge research, and help shape the future of prostate cancer care.
The post holder will work under the supervision of the senior research nurse or Study Site Coordinators (SSC) within the research team and has a key role to play in the day-to-day running of clinical trials within the Trust. These trials may be related to anti-cancer treatment (e.g. chemotherapy, radiotherapy, biological therapy, gene therapy or surgery), symptom management or some other aspect of cancer care, such as screening. Central to the role are the recruitment, education and monitoring of patients entering a clinical trial. Working closely with the principal investigator and members of the multidisciplinary team, they will support patients who choose to participate in clinical trials by providing advice and information and acting as the patients’ advocate. An important aspect of the role is the maintenance of accurate and comprehensive records of data derived from the research studies. The post holder will be involved in ensuring that any research undertaken within the department safeguards the well being of the patients, and is conducted within ICH Good Clinical Practice Guidelines for Research.
The research nurse may contribute to the development of the trial design and has a key role in incorporating the patients and nurses perspective. Liaison with pharmaceutical companies and academic institutions during trial development will be required.
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.
For further information on this role, please see the attached detailed Job Description and Person Specification:
Research (Clinical Research)
2.1 To coordinate arrangements required for patients undergoing specialist investigations as part of the research protocol.
2.2 To assess the patient prior to trial treatment, monitor the patient receiving trial treatment and follow the patient up on completion of trial treatment as required by protocol.
2.3 To collect and accurately record data in accordance with requirements of the trial protocol.
2.4 To participate in the design and preparation of research protocols, patient information sheets and other documentation associated with clinical trials, ensuring that these are reviewed and updated as required.
2.5 To safeguard the integrity of the trial by ensuring compliance with ICH GCP guidelines.
2.6 To be involved with the running of several concurrent research studies.
2.7 To disseminate research data by preparing and presenting posters or research papers for presentations at meetings, conferences and publication.
This advert closes on Monday 11 May 2026
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