Clinical Research Nurse

The Royal Marsden Nhs Foundation Trust

Greater London

On-site

GBP 36,000 - 48,000

Full time

14 days+
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Benefits offered by this job

Flexible working requests

Job summary

The Royal Marsden NHS Foundation Trust is seeking a Band 6 Clinical Research Nurse for a 12-month maternity cover with the CTUUC in Chelsea. The role focuses on urological cancer trials, delivering care to patients enrolled in clinical research within a fast-paced multidisciplinary environment.

We require oncology nursing expertise, clinical research experience, and UK registration. You will manage your own caseload, ensure protocol adherence, and contribute to research data quality and

Qualifications

  • Post-registration oncology qualification or equivalent.
  • Proficiency in data collection and trial documentation.
  • Experience as a senior nurse in a clinical research environment.
  • Experience in oncology nursing and UK registration.

Responsibilities

  • Coordinate arrangements for patients undergoing specialist investigations per protocol.
  • Assess, monitor, and follow up patients during and after trial treatment.
  • Collect and record data in accordance with trial requirements.
  • Contribute to design and preparation of trial documentation.
  • Ensure compliance with ICH GCP guidelines to safeguard trial integrity.

Skills

Oncology nursing
Senior nurse experience
Research methods training
Data collection

Education

Post registration oncology qualification
Degree level or equivalent

Tools

Access
Excel
SPSS

Job description

Job summary

Band 6 Clinical Research Nurse (12-Month Maternity Cover)

An exciting opportunity has arisen for a Band 6 Clinical Research Nurse to join Clinical Trials Unit Urology Chelsea (CTUUC) on a 12-month maternity cover contract.

Our team specialises in prostate, bladder, and urothelial cancers and operates within a highly regarded, fast-paced multidisciplinary environment. Recognised as leaders in the management of urological cancers, we are committed to delivering outstanding patient care alongside pioneering clinical research.

The successful candidate will manage their own caseload of patients enrolled in clinical trials, working closely with both research and clinical colleagues to ensure the highest standards of care. Previous oncology experience is essential, while experience in clinical research is desirable. Applicants should be educated to degree level or possess an equivalent qualification.

You will be responsible for delivering research care in accordance with clinical trial protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. We are seeking an enthusiastic and motivated individual who can work independently as well as collaboratively within a multidisciplinary team. Excellent communication, organisational, administrative, and IT skills are essential, together with a positive attitude and a willingness to embrace new challenges and initiatives.

Main duties of the job

CTUUC manages a broad and growing research portfolio, encompassing commercial and non-commercial clinical trials, investigator-led studies, translational research incorporating genetic components, and observational studies. This diverse programme offers a unique opportunity to contribute to cutting-edge research while developing specialist expertise in uro-oncology. Maintaining high-quality data collection, proactive patient screening, and exceptional patient care are central to the success of our research programme.

The post also provides continuity of care and ongoing support for patients who often require long-term follow-up and close clinical monitoring throughout their treatment journey.

What We Offer

  • Opportunities to develop and enhance your clinical and research skills
  • Access to a wide range of internal and external professional development opportunities
  • The chance to work as a valued member of an expert multidisciplinary team
  • Involvement in innovative research that has the potential to improve outcomes for patients with urological cancers
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.

Job responsibilities
  • 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
  • Post registration oncology qualification or equivalent relevant qualification
  • Basic computer Literacy
  • Research methods education
  • Evidence of Continuing Professional Development
  • Competence in research orientated PC software (Access, Excel, SPSS)
  • 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
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).

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