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Job summary

Main area
Gastrointestinal
Grade
NHS AfC: Band 6
Contract
Permanent
Hours
Full time - 37.5 hours per week
Job ref
282-CR1175
Employer
The Royal Marsden NHS Foundation Trust
Employer type
NHS
Site
Royal Marsden Hospital Chelsea
Town
Chelsea
Salary
£46,419 - £55,046 Per Annum
Salary period
Yearly
Closing
02/02/2026 23:59

Employer heading

The Royal Marsden NHS Foundation Trust logo

Research Nurse - Gastrointestinal

NHS AfC: Band 6

Job overview

We are looking for an enthusiastic and motivated oncology nurse to join the GI and Lymphoma Research team.  They will undertake the role of the key worker supporting all patients entering clinical trials in the unit. 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.  

Liaison with pharmaceutical companies and academic institutions during trial development will be required. There will be the  opportunity to attend study days, further education courses and conferences relevant to the speciality.

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, you 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.

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 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.
  • To be involved with the running of several concurrent research studies.
  • To disseminate research data by preparing and presenting posters or research papers for presentations at meetings, conferences and publication.

Person specification

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
Desirable criteria
  • Relevant diploma / degree
  • Competence in research orientated PC software (Access, Excel, SPSS)

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.
  • Previous experience in clinical speciality of post applied for e.g. haematology, gynaecology, palliative care.
  • Personal and Leadership Management experience.
Desirable criteria
  • Experience of co-ordinating IRAS 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.
  • Ability to innovate and respond to change.
  • Able to work unsupervised.
Desirable criteria
  • Ability to initiate and drive original research.

Employer certification / accreditation badges

Trust IDApprenticeships logoLondon Living Wage is a voluntary commitment made by employers, who can become accredited with the Living Wage FoundationArmed Forces Covenant Gold AwardDisability confident employerCare quality commission - OutstandingStep into health

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

Apply online now

Further details / informal visits contact

Name
Julie Martin
Job title
Lead GI and Lymphoma Research Nurse
Email address
[email protected]