Clinical Research Nurse​/Practitioner

Delivery of the service level agreement with the East of England Regional Research Delivery Network (EoE RRDN) is an essential component of this role. Main duties and responsibilities The role involves using in-depth knowledge of trial protocols and their application in practise, research methodology and an in-depth working knowledge of local, national and international research regulation requirements to implement, develop and facilitate the smooth running of clinical trials, working collaboratively as part of the research team within Milton Keynes University Hospital.

This will involve ensuring compliance with all regulatory standards and best practices, while supporting the overall research objectives and contributing to the delivery of high-quality research outcomes. This will include:
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. Communication Promote trial involvement throughout the clinical and patient communities;
Explain trials including complex trials in an unbiased sensitive way to emotive patients. Being able to display empathy and understanding. Liaise and discuss trials including complex trial issues, with members of the MDT before, during and after the clinical trial. Education 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.

Educating others 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. Professional 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. Management 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.

To co-ordinate all aspects of conducting a clinical trial and research project always ensuring that trial participants are fully informed of what is required. Please refer to the Job Description for further details

Milton Keynes University Hospital NHS Foundation Trust

Milton Keynes University Hospital NHS Foundation Trust

Milton Keynes University Hospital NHS Foundation Trust