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Clinical Research Nurse

Applications are closed

  • Job
    Full-time
    Mid & Senior Level
  • Healthcare
  • London

Requirements

  • Applicants must be a registered adult nurse with evidence of continuing professional development.
  • You should have good experience in working within the NHS, a strong clinical background and a desire and willingness to learn & develop others.
  • Candidates must demonstrate excellent communication and interpersonal skills, and have the ability and initiative to work independently and manage a patient caseload across a variety of research studies.
  • Keep up to date with current practices for cannulation, phlebotomy, care of patients with Central Venous Access lines and handling and administration for cytotoxic chemotherapy.
  • Act as a role model for excellence in oncology based research.

Responsibilities

  • Work within EU clinical trial directives in accordance with ICH GCP (International Conference on Harmonisation and Good Clinical Practice) ensuring that the clinical trial protocol is adhered to at all times.
  • Identify patients suitable for entry into clinical trials by attending clinics (screening notes/consultant referral) and Multidisciplinary Team (MDT) meetings.
  • Participate in the informed consent process acting as a resource and support to patients and their families.
  • Co-ordinate the research patient pathway from screening through to trial closure.
  • Ensures that adequate precautions are taken to minimise the risk of cross-infection in relation to the safe disposal of body fluids including blood products.
  • Advise the local nursing team who administer trial drugs, be aware of and report any side effects as outlined in the protocol.
  • Maintain adequate patients’ records and ensure all relevant information is documented in the patient’s medical and nursing notes.
  • Responsible for accurate completion of Clinical Report Forms (CRFs).
  • Responsible for the collection, co-ordination and computerisation of data generated from the clinical trials.
  • Keep up to date with current practices for cannulation, phlebotomy, care of patients with Central Venous Access lines and handling and administration for cytotoxic chemotherapy.
  • Act as a role model for excellence in oncology based research.

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.

Our values: put patients first, take pride in what we do, respect others, act with integrity, strive to be the best. 💙

Science & Healthcare
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Mission & Purpose

Guy's and St Thomas' NHS Foundation Trust is a leading healthcare provider in the UK, offering a wide range of medical services through its hospitals and community services. The Trust is dedicated to providing high-quality, compassionate care to patients while advancing medical research and education. Their ultimate mission is to improve health outcomes and enhance the well-being of the communities they serve. The Trust is committed to innovation, excellence in care, and ensuring equitable access to healthcare for all.

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