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Senior Research Nurse/Practitioner | The Royal Marsden NHS Foundation Trust
| Dyddiad hysbysebu: | 10 Mehefin 2024 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | £40,701 - £48,054 Per Annum Inc HCAS |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 10 Gorffennaf 2024 |
| Lleoliad: | Sutton, SM2 5PT |
| Cwmni: | The Royal Marsden NHS Foundation Trust |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | 6379950/282-CR1245950 |
Crynodeb
Our Breast Radiotherapy team is due to conduct a commercial trial at RM, CCR6008 GUARD. This trial requires a research nurse/clinical research practitioner to run this study, closely supervise patients during the application of a topical gel (drug) prior to each dose of radiotherapy, monitor skin and systemic toxicities for all participants as well as collecting blood samples and monitoring vital signs before and after each treatment during the safety run-in phase of the trial. These are all tasks that the existing administrative research staff in our team cannot undertake, and we therefore need to employ a clinical research nurse/research practitioner for 12 months for the safe and successful delivery of this trial.
The post holder will work under the supervision of the Team Leader or Senior Research Coordinator, 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, s/he 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 opportunity to undertake personal research projects or further study, in consultation with the lead medical investigator and Senior Nurse, Clinical Trials is also encouraged.
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 Day care 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.
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/translational 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/translational trial, of voluntary entry to the 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 trial.
• To monitor treatment toxicity and/or side effects and to take appropriate action to reduce the effects of treatment as necessary.
• To report to the principal investigator or senior research nurse any adverse events and serious adverse events that occur whilst the patient is being treated on a clinical trial and record relevant details.
This advert closes on Monday 24 Jun 2024
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