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Job summary

Main area
Gynaecological Cancer Research
Grade
NHS AfC: Band 7
Contract
Fixed term: 12 months
Hours
Full time - 37.5 hours per week
Job ref
282-CR1246010
Employer
The Royal Marsden NHS Foundation Trust
Employer type
NHS
Site
The Royal Marsden Hospital Chelsea
Town
Chelsea
Salary
£51,488 - £57,802 per annum incl. HCAS
Salary period
Yearly
Closing
15/07/2024 23:59

Employer heading

The Royal Marsden NHS Foundation Trust logo

Research Nurse

NHS AfC: Band 7

Job overview

The post holder will be working with the multi-disciplinary team in the Gynae unit at the  Royal Marsden NHS Foundation Trust in Sutton. We are a highly regarded busy multidisciplinary team performing both clinical and research work and are seen as pioneers in managing Gynae cancer treatment. They will manage their own caseload of patients on clinical trials with the support of the research team.   

Ideally with previous clinical research experience and preferably educated to degree level, 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.

The successful applicant should have a flexible approach to their duties and the ability to work both as part of the team as well as independently.  In addition; excellent communication, administrative and IT skills and being supportive and open to new initiatives are particularly valued by the team.
It would be an advantage to have research and Gynea experience. The successful candidate will be required to work as a self directed practitioner and have the skills to motivate others. 

This is a cross-site role and applicants are expected to travel between our Chelsea and Sutton Sites. x3 days at Chelsea and x2 days at Sutton

Main duties of the job

  • 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 further information on this role, please see the attached detailed Job Description and Person Specification:

  • To provide advice and information to patients/volunteers with regard to their participation in clinical research in order to facilitate effective informed consent, ensuring the patient (or where appropriate the parent/ guardian or next of kin) fully understands the nature of the clinical trial, of voluntary entry to the clinical trial and freedom to withdraw at any time without prejudice to treatment.
  • 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 assist the medical team in the assessment of patients/volunteers and monitoring their condition throughout their participation in the clinical trial.

 

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

Employer certification / accreditation badges

Apprenticeships 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
Melody Ncube
Job title
Lead Clinical Research Nurse
Email address
[email protected]

If you have problems applying, contact

Address
Recruitment Support Team
Telephone
01629 690825
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