FAQs
What qualifications do I need to apply for the Clinical Research Nurse position?
Applicants must be a registered adult nurse with evidence of continuing professional development and a strong clinical background.
Is experience within the NHS required for this role?
Yes, candidates should have good experience working within the NHS.
What are the main responsibilities of the Clinical Research Nurse?
Key responsibilities include identifying suitable patients for clinical trials, participating in the informed consent process, coordinating the research patient pathway, and ensuring adherence to clinical trial protocols.
Will I have opportunities for professional development in this role?
Yes, the role offers opportunities to learn about different tumour groups and gain knowledge in various systemic anti-cancer therapies.
What type of studies will I be involved with as a Clinical Research Nurse?
You will be involved with a growing portfolio of Oncology and Haemophilia Clinical Research studies, including Phase II and III trials as well as early-phase clinical trials.
How does the OHCT team work with other departments?
The OHCT team collaborates closely with oncology and haematology medical teams to recruit patients for trials and monitor them throughout the study.
Who can I contact for further details or an informal visit regarding this role?
You can contact Ida Williams, OHCT Practice Development Nurse, at Ida.Williams@gstt.nhs.uk for further details or to arrange an informal visit.
What is the mission statement of the Oncology and Haematology Clinical Trials team?
The mission statement is ‘Improving treatment choice, clinical care and outcomes for cancer patients through innovation, dedication and excellence in clinical trials.’
Will I be required to manage a patient caseload?
Yes, you will be expected to manage a patient caseload across a variety of research studies independently.
Are there specific protocols I need to adhere to in this role?
Yes, you must work within EU clinical trial directives in accordance with ICH GCP and ensure that the clinical trial protocol is adhered to at all times.