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Clinical Research Nurse | Chelsea and Westminster Hospital NHS Foundation Trust

Job details
Posting date: 23 May 2024
Salary: Not specified
Additional salary information: £32,720 - £39,769 Per annum
Hours: Full time
Closing date: 22 June 2024
Location: Isleworth, TW7 6AF
Company: Chelsea and Westminster Hospital NHS Foundation Trust
Job type: Permanent
Job reference: 6270982/289-CR-1570

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Summary


An exciting opportunity has arisen for a dynamic and enthusiastic nurse to join the Research team at West Middlesex University Hospital. We welcome applications from experienced nurses with recent knowledge and skills acquired in acute settings, who can demonstrate an understanding of the importance of clinical trials plus a genuine interest and commitment to the specialist role of the research nurse. The job entails assisting the existing Research team in clinical and administrative activities related to clinical trials, from initiation to termination, in accordance with International Council for Harmonisation and Good Clinical Practice guidelines (ICH-GCP).



The post holder will be expected to work at West Middlesex University Hospital. This is a permanent full time Band 5 post and offers the candidates the opportunity to enhance career in clinical research. The post holder is expected to ensure that all research processes are in accordance within the remits of research guidelines. The safety and well being of the study participant is paramount at all times. The post holder will work across the three clinical divisions of the Trust- Planned Care, Emergency & Integrated Care and Specialist Care.

Chelsea and Westminster Hospital NHS Foundation Trust is proud to be one of the top performing and safest trusts in England. We have two main acute hospital sites—Chelsea and Westminster Hospital and West Middlesex University Hospital, plus our award-winning clinics across North West London and beyond.

The post holder will assist under the guidance of more experienced colleagues with the set-up, maintenance, and close down of clinical studies in accordance with local, national and international legislation within various clinical areas. The post will entail assessing patient’s suitability, ensuring informed consent is obtained, coordinating the logistics for patient visits and undertaking patient assessments in accordance with study protocol. All data will be recorded including adverse and serious adverse events in accordance with ICH-GCP. It will be the post holder’s responsibility to ensure studies are delivered in line with agreed targets.


This advert closes on Wednesday 5 Jun 2024

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