Job summary An exciting opportunity has arisen for a Breast Research Nurse to join the Breast Research unit at The Royal Marsden in Sutton. We are looking for enthusiastic and self-motivated nurses to contribute to the ground-breaking research run out of this unit. The post holder should have experience in clinical research nursing and/or oncology. You will work within the guidelines and policies for the conduct of clinical trials, ensuring high standards of practice in accordance with the principles of GCP. You will work under the supervision of the Senior Breast Research Nurses. They should also have a flexible approach to their duties and the ability to work both as part of the team as well as independently. In addition, you will have excellent communication and be supportive and open to new initiatives. Prior enquires welcome and encouraged. Main duties of the job 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, s/he 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. 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. Date posted 17 April 2025 Pay scheme Agenda for change Band Band 6 Salary £42,939 to £50,697 a year Per Annum Contract Fixed term Duration 11 months Working pattern Full-time Reference number 282-CR416 Job locations Royal Marsden Hospital Sutton Sutton SM2 5PT Job description Job responsibilities For further information on this role, please see the attached detailed Job Description and Person Specification: To coordinate arrangements required for patients undergoing specialist investigations as part of the research protocol. 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. To collect and accurately record data in accordance with requirements of the trial protocol. 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. To safeguard the integrity of the trial by ensuring compliance with ICH GCP guidelines. Job description Job responsibilities For further information on this role, please see the attached detailed Job Description and Person Specification: To coordinate arrangements required for patients undergoing specialist investigations as part of the research protocol. 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. To collect and accurately record data in accordance with requirements of the trial protocol. 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. To safeguard the integrity of the trial by ensuring compliance with ICH GCP guidelines. Person Specification Education/Qualifications Essential First level registration Post registration oncology qualification or equivalent relevant qualification Basic computer Literacy Research methods education Evidence of Continuing Professional Development Desirable Relevant diploma / degree Competence in research orientated PC software (Access, Excel, SPSS) Experience Essential Experience as a senior staff nurse or above working in a clinical research environment Experience as a senior staff nurse in oncology nursing Desirable Previous experience in clinical speciality of post applied for e.g. haematology, gynaecology Personal and Leadership Management experience Experience of co-ordinating HRA submissions Person Specification Education/Qualifications Essential First level registration Post registration oncology qualification or equivalent relevant qualification Basic computer Literacy Research methods education Evidence of Continuing Professional Development Desirable Relevant diploma / degree Competence in research orientated PC software (Access, Excel, SPSS) Experience Essential Experience as a senior staff nurse or above working in a clinical research environment Experience as a senior staff nurse in oncology nursing Desirable Previous experience in clinical speciality of post applied for e.g. haematology, gynaecology Personal and Leadership Management experience Experience of co-ordinating HRA submissions 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. UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Additional information 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. UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Employer details Employer name The Royal Marsden NHS Foundation Trust Address Royal Marsden Hospital Sutton Sutton SM2 5PT Employer's website https://www.royalmarsden.nhs.uk/working-royal-marsden (Opens in a new tab)