Clinical Research Nurse | University Hospital NHS Foundation Trust

Clinical Research Nurse

Department:
Research & Development

Band 6: £37,338- £44,962

Hours:

22.5 hrs/wk

Fixed Term Contract until 25/11/2026

This is an exciting opportunity for a registered nurse, educated to a degree level, with substantial clinical nursing experience to work in research delivery to cover maternity leave. We are looking for someone who can multitask, is resourceful, patient‑centred and able to work in clinical settings as well as an office (IT, e‑calendars, virtual meetings, data management, etc). Prior experience in research delivery is prioritised.

The post holder will join our team and work towards set‑up, delivery, and follow‑up of research studies across various specialties, hence the requirement for a sound clinical base, ability to process complex information and assuredness. Due to the nature of research your workload will cover different specialties and may vary depending on the need in the department.

However, gaining insight and experience into research governance, delivery and process which leads to evidence‑based practice is a great addition to your career and strengthens your communication, organisational skills and multidisciplinary work.

Sponsorship is not available currently.

For an informal discussion, please contact Reema Alen Babu – Senior Research Nurse,

Interview date: 17.02.2026

Milton Keynes University Hospital NHS Foundation Trust is a University Teaching Hospital committed to advancing patient care through cutting‑edge research and education.

• Review each trial protocol to identify resource implications for Milton Keynes University Hospital NHS Foundation Trust.
• Ensure all regulatory approvals are in place prior to commencement of study (e.g. research ethics committee and Trust R&D permission).
• Identify eligible patients for trials by attending clinics, multidisciplinary team (MDT) meetings, screening lists, and assessing clinical condition of patient in detail.
• Promote trial involvement throughout the clinical and patient communities; explain trials including complex trials in an unbiased sensitive way to emotive patients, displaying empathy and understanding.
• Liaise and discuss trials including complex trial issues with members of the MDT before, during and after the clinical trial.

• Promote trial involvement and explain complex trials in an unbiased sensitive way to emotive patients.
• Liaise with MDT and discuss trial issues.

• Attend the trial investigator / research nurse/practitioner meetings and conferences when required.
• Maintain awareness of current advances in medical treatments, research, and nursing practice (nurses only) and use this specialised knowledge to develop and maintain high standards of care for patients.
• Participate in formal and informal teaching programmes, study days and educational programmes within the Trust, as arranged by EoE RRDN/Divisions and elsewhere as appropriate.
• Identify personal training requirements and initiate appropriate training with line manager approval.

• Participate in the preparation and delivery of research education and training programmes to all relevant healthcare staff with Milton Keynes University Hospital and EoE RRDN as appropriate.
• Support, supervise and manage student placements, shadowing opportunities and junior members of the team.
• Disseminate research findings by developing and presenting posters / research papers for meetings, conferences, and publication; circulate trial information and carry out presentations locally.

• Act in accordance with the NMC Code of Professional Practice for Nurses, Midwives and Health Visitors and Scope of Professional Practice (nurses only) or relevant professional body.
• Maintain registration on the Clinical Research Practitioner directory and awareness of, and involvement in CRP initiatives (as relevant).
• Maintain one's own professional development, maintaining a contemporary personal portfolio.

• Ability to work independently and be accountable for own professional actions. Self‑manage all work areas and workload, seeking managerial supervision as required. Maintain own time schedule and ensure that all timelines are adhered to.
• Coordinate all aspects of conducting a clinical trial and research project, always ensuring that trial participants are fully informed of what is required.
• Be aware of all Trust procedures and policies and collaborate with other healthcare professionals to ensure these are observed; participate in the development of Trust procedures and policies as required.

Please refer to the job description for further details.

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