Clinical Research Nurse Specialist

1 month ago

London, Greater London, United Kingdom Guy's and St Thomas' NHS Foundation Trust Full time
Job Summary

We are seeking a highly skilled and experienced Clinical Research Nurse to join our team at the NIHR Clinical Research Facility (CRF) at Guy's and St Thomas' NHS Foundation Trust. As a Clinical Research Nurse, you will play a key role in ensuring the safe and effective conduct of clinical trials, working closely with multidisciplinary teams to deliver high-quality patient care.

About the Role

The successful candidate will have extensive experience of working within a ward environment as a qualified nurse, with a strong background in clinical research and a proven track record of effective multidisciplinary team working. You will be responsible for assessing, planning, implementing, and evaluating expert research nursing care, as well as providing support to patients attending the Department who have been or have the potential to be recruited onto a clinical trial programme.

Key Responsibilities
  • Recruit to and follow up patients within studies, including randomized clinical trials and other high-quality clinical studies.
  • Act as a patient advocate, enabling patients to make informed choices concerning their involvement in clinical trials and ensuring advice and information is provided.
  • Ensure there is sufficient skill mix of staff for patient safety during clinical trials and ensuring that they are carried out within the Trust and Centre's policies and clinical trial protocol.
  • Assist in clinical trials, including venepuncture and cannulation of volunteers when necessary, ensuring that they are carried out within the Trust's policies, research governance, Medicines for Human Use (Clinical Trials Regulations) Incorporating International Conference on Harmonisation of Good Clinical Practice (ICH GCP) and Data Protection Act.
  • Undertake clinical tasks such as phlebotomy, analysis of blood specimens, drug administration, and clinical observation, and advise staff, both registered and unregistered, in the delivery of care to the volunteer.
  • Ensure that written informed consent has always been obtained for any treatment provided for, or any sample or data taken from a volunteer, which will form part of a research study, in accordance with the Trust research governance arrangements and Medicines for Human Use (Clinical Trials Regulations) Incorporating International Conference on Harmonisation of Good Clinical Practice (ICH GCP).
  • Maintain all data and case report forms relating to clinical trials in accordance with the Medicines for Human Use (Clinical Trials Regulations) Incorporating International Conference on Harmonisation of Good Clinical Practice (ICH GCP).
  • Deal with concerns raised by volunteers and visitors in a proactive manner and take remedial action as necessary.
  • Act as the volunteer's advocate.
Requirements

The ideal candidate will have a Level 1 NMC Registered Nurse qualification, educated to degree level or above, with relevant specialist course or equivalent experience (e.g. SACT). They will also have extensive experience of working within a ward environment as a qualified nurse, with a strong background in clinical research and a proven track record of effective multidisciplinary team working.

What We Offer

We offer a competitive salary and benefits package, as well as opportunities for professional development and career progression. You will be working in a dynamic and supportive team environment, with access to state-of-the-art facilities and world-leading expertise.

How to Apply

If you are a motivated and experienced Clinical Research Nurse looking for a new challenge, please submit your application, including your CV and a covering letter, to [insert contact details]. We look forward to hearing from you.

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