Job summary
- Main area
- Lung Research
- Grade
- NHS AfC: Band 7
- Contract
- 11 months (Fixed term: 11 months)
- Hours
- Full time - 37.5 hours per week
- Job ref
- 282-CR1249
- Employer
- The Royal Marsden NHS Foundation Trust
- Employer type
- NHS
- Site
- The Royal Marsden Hospital
- Town
- Sutton
- Salary
- £47,810 - £54,710 per annum
- Salary period
- Yearly
- Closing
- 27/02/2026 23:59
Employer heading
Senior Research Nurse
NHS AfC: Band 7
Job overview
An opportunity has arisen for a Band 7 Clinical Research Nurse post within the Lung Unit working in our Chelsea site. The role will provide opportunities and exposure to the whole clinical research portfolio working alongside experts in medical oncology and clinical research nursing. We are a highly regarded busy multidisciplinary team performing both clinical and research work and are seen as pioneers in managing lung cancer cancer treatment.
The experienced research nurse works as a self-directed practitioner, with a key role to play in the organisation and management 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. You will take responsibility for the co-ordination and management of a clinical research portfolio, collaborating with key personnel to ensure continued care and support for patients involved in clinical trials.
Main duties of the job
The experienced research nurse works as a self-directed practitioner, with a key role to play in the organisation and management of clinical trials within the Trust.
The post holder will support more junior research nurses, assisting them to develop their clinical research skills thorough education and training. Further responsibility will include monitoring and raising the standard of nursing input within the team.
The opportunity to undertake personal research projects or further study, in consultation with the lead medical investigator and Senior Nurse, Clinical Trials, is also encouraged. Main duties include:
- 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.
Working for our organisation
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.
Detailed job description and main responsibilities
For more information please refer to the Job Description & Person Specification.
- To assess and evaluate the progress of on-going clinical trials and research undertaken in the unit, maintaining an accurate account of the status of the projects and to regularly update the department on the status.
- To liaise with pharmaceutical sponsors regarding feasibility and implementation aspects of proposed clinical trials.
- To ensure that all ICH GCP required documentation is kept in a clearly trackable system and is stored in an appropriate manner for the appropriate length of time.
- To act as a support for patients and relatives throughout the trial, providing information as well as physical, spiritual and emotional support where necessary, and referring to other healthcare professionals where appropriate.
- To work effectively as part of the multidisciplinary team and to contribute to the ongoing development of the clinical unit by acting as a role model for staff in areas related to clinical trials.
- To educate and update staff working in the particular clinical area or research team about current and forthcoming clinical trials, including treatment administration, potential side effects, and monitoring required.
Person specification
Education/Qualifications
Essential criteria
- Relevant diploma / degree
- Competence in research orientated PC software (Access, Excel, SPSS)
Education/Qualifications
Essential criteria
- First level registration
- Post registration oncology qualification or equivalent relevant qualification
- Basic computer Literacy
- Research methods education
- Evidence of Continuing Professional Development
Experience
Essential criteria
- Experience as a senior staff nurse or above working in a clinical research environment
- Experience as a senior staff nurse in oncology nursing
Desirable criteria
- Previous experience in clinical speciality of post applied for e.g. haematology, gynaecology
- Personal and Leadership Management experience
- Experience of co-ordinating HRA submissions
Skills/ Abilities / Knowledge
Essential criteria
- Proven experience of team leadership and team building initiatives
- Advanced organisational skills and ability to managed multiple projects at various stages of development and organisation
- Excellent cross-disciplinary /interagency communication skills and ability to facilitate collaborative working relationships
- Ability to appraise junior staff through performance review
- Confident and articulate
- Ability to make decisions, organise and prioritise
- Able to work unsupervised
Desirable criteria
- Ability to initiate and drive original research
Other
Essential criteria
- Flexibility to meet the needs of the service (e.g. shift work)
Desirable criteria
- Able to work on both sites and to be flexible to meet the needs of the role
Applicant requirements
You must have appropriate UK professional registration.
This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.
Documents to download
Further details / informal visits contact
- Name
- Derya Sahin
- Job title
- Lead Research Nurse Chelsea
- Email address
- [email protected]
- Additional information
For more information or to come and see our unit please contact, Derya Sahin Lead research Nurse -02089154003
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