Are you an experienced research nurse looking to make a real impact in oncology? Join our prostate research team at the West Wing Clinical Research Centre as a Band 6 Research Nurse. You will lead patient care across an expanding portfolio of clinical trials, from study set‑up to treatment delivery and follow‑up. This is a unique opportunity to work in a dynamic, supportive team, contribute to cutting‑edge research, and help shape the future of prostate cancer care.
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, they 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.
The research nurse may contribute to the development of the trial design and has a key role in incorporating the patients and nurses perspective. Liaison with pharmaceutical companies and academic institutions during trial development will be required.
Research (Clinical Research)
* Coordinate arrangements required for patients undergoing specialist investigations as part of the research protocol.
* 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.
* Collect and accurately record data in accordance with requirements of the trial protocol.
* 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.
* Safeguard the integrity of the trial by ensuring compliance with ICH GCP guidelines.
* Be involved with the running of several concurrent research studies.
* Disseminate research data by preparing and presenting posters or research papers for presentations at meetings, conferences and publication.
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