0-19 Paediatric Research Health Visitor/Nurse/AHP
| Dyddiad hysbysebu: | 27 Ebrill 2026 |
|---|---|
| Cyflog: | £39,959.00 i £48,117.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £39959.00 - £48117.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 11 Mai 2026 |
| Lleoliad: | Knaresborough, HG5 8QB |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | C9421-26-0267 |
Crynodeb
Promoting Research Engagement and Communication Through collaborative partnership working build relationships to promote and secure engagement and involvement in 0-19 and paediatric studies. To identify and participate in local, regional and national networks establishing links to promote access and involvement in research. To develop research capacity, capability and competence within the 0-19 and paediatric areas to recruit patients / participants and carry out NIHR Portfolio studies. Promote the work of the research service within the Trust and the Yorkshire and Humber Regional Research Network and contribute to its development. Liaise with and develop links between practitioners in primary and secondary care, public health, social care and 0-19 areas. Raise the profile of clinical research by educating clinical staff and patients about research. The postholder will establish and develop a bespoke user group to promote user involvement. Participate as a representative of the R&I team at local, regional and national meetings. Education and Training Through mentoring and coaching support 0-19 and paediatric colleagues to become research-ready building research capacity, capability and competency. Develop a research active culture through workforce development, measured by an increased number of staff holding GCP, gaining experience in research study activity. Utilise staff feedback on their experiences of being involved in research to foster research engaged culture. Contribute to staff and student development activities regarding research within the R&I department and at a wider trust level. Develop academic links to facilitate collaboration for research and clinical practice. Maintain registration with the Nursing and Midwifery Council (NMC), Health Care and Professions Council (HCPC) as appropriate by actively engaging in continuing professional development. Research set up, initiation and delivery To manage studies in collaboration with existing research delivery team, acting as a main point of contact for participants and carry out related activities including: Increase the number of research studies delivered in the wider 0-19 health and care setting through research delivery. Increase research participation through increased recruitment particularly in hard-to-reach populations such as those in our rural and coastal communities, ensuring fair and equitable access to research participation opportunities. Be responsible for regularly contributing to research activity by setting up and managing a portfolio of studies. Drive improvements in study time set up expediating timescales from the point of the submission of an expression of interest (EOI) through to study opening and attaining research time in target (RTT). Working close with a study / trial Principal Investigator (PI) to provide a consistent point of contact for the trial. Become familiar with the protocol for a trial / study to ensure optimised delivery. Identify patients who may be suitable for the trial liaising with clinicians and attending clinical team meetings to promote research participation and remind clinical team members about the requirements for a trial / study. Work with the trial / study investigators to recruit patients to studies / trials where appropriate and manage performance of the study. Give information to potential trial / study participants considering participation, answer questions and refer to the Principal Investigator (PI) where required. Ensure that all consent procedures are carried out in strict accordance with the relevant study / trial protocol complying with Good Clinical Practice principles. Undertake clinical procedures within the study / trial participants as appropriate, including taking bloods. Obtain clinical specimens from participants, store and package them as required and organise their safe and timely delivery to the appropriate laboratory. Liaise with clinical staff to ensure the timely administration of investigation, treatment and follow-up required for studies / trials. Contribute to trial pharmacovigilance by being aware of safety reporting procedures and classifications per Good Clinical Practice (GCP) guidance, i.e. for adverse events, ensuring prompt recording and reporting both within the Trust and to regulatory authorities as the nature of the event requires. Complete case report forms and all trial documentation accurately and promptly. Maintain trial files and ensure they are always up to date. Act as a primary contact for participants in designated trials / studies. Maintain contact with participants during trial procedures and follow-up, including home visits where appropriate; provide advice and emotional support as required and ensure participants are kept fully informed and are able to take part in decisions about their care within the trial. Use software for data inputting, data management, reporting as required. Work to the requirements of trial protocols, the Good Clinical Practice Guidelines applicable to the study and the UK Policy Framework for Health and Social Care Research (2017). Work with the R&I office to facilitate research governance approval processes and trial finance. Assist with monitoring visits conducted by Sponsors or their nominated representatives. Facilitate inspections by the Medicines and Healthcare Products Regulatory Agency as required, answering Inspectors questions about trial conduct, contributing to response made to any findings and ensuring appropriate modifications to procedures are made in a timely fashion, particularly in relation to critical or major findings. Carry out any other trial / study related duties within the post holders qualifications and competence as delegated by the Research and Innovation Manager / Senior Research Nurse(s) or the relevant trials Principal Investigator. Line manages Clinical Trial Assistant(s), Research practitioner/s and or band 5 Research Nurses. Report monthly recruitment figures to the governance team, Senior research nurse and research and innovation manager. For further information please see the Job Description and Personal Specification attached.