Research Nurse
| Dyddiad hysbysebu: | 26 Ionawr 2026 |
|---|---|
| Cyflog: | £31,049.00 i £37,796.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £31049.00 - £37796.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 06 Chwefror 2026 |
| Lleoliad: | Sheffield, S4 7QQ |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | C9457-26-0020 |
Crynodeb
To maintain a suitable environment to promote the well-being and safety of patients, participants and staff, identifying the need for further risk assessment where necessary. To assess the suitability of patients for referral into the clinic and suitability of patients for current and future studies To provide patients taking part in clinical trials with specialist information regarding their participation, including risk. To provide high standards and continuity of care for participants during the research study, maintaining lines of communication with clinical staff. To act as a resource to patients, their families and staff from within the clinical area, and to act as an effective referral to other support agencies where necessary. To assist participants with data collection, such as completion of questionnaires, and interviews, as necessary. To organise and manage defined procedures, assist with interventional treatments and record the resulting information. To develop knowledge and skills to become a competent research practitioner through research training opportunities. To assist the Research Manager, and wider research team and other services involved in the set up and delivery of research studies. To work as part of a team to co-ordinate and manage research within expected timelines. To work with colleagues in identifying, screening and recruiting research participants, working collaboratively to recruit to time and target.To co-ordinate participant visits, providing support to participants, and other team members. To participate in the process of initial and ongoing informed consent of participants prior to carrying out procedures and treatments as agreed within the trial protocol. To identify areas of low patient recruitment and liaise with the team to identify strategies for improving recruitment, providing verbal/ written reports where requested. To work at all times in accordance with Good Clinical Practice, Research Governance and current legislation/Trust policies when collecting data and delivering research, ensuring ethical and clinical safe practice. To understand the requirements of the study protocol and to adhere to them, for example when conducting assessment and follow-ups. Ensuring adherence and escalating where appropriate. To ensure that updates and study amendments are reported in a timely fashion, and to further support with site file management. To attend multidisciplinary team meetings regularly to discuss progress with recruitment, research protocols and other essential topics. To provide information as needed when the team is completing feasibility assessments of potential new studies in the Trust, led by the Research Manager and Research Delivery Manager. To provide support for research projects to obtain approvals from the Health Research Authority and NHS Ethics. To pay meticulous attention to detail when preparing patient documentation, completing accurate records of patient care, maintaining source data and case report forms (CRF) in a clearly trackable system, to ensure data validity. To upload data promptly to the RDU Local Performance Monitoring System (EDGE) To promptly report potential Serious Adverse Events (SAEs) to a senior member of the team to establish need for escalation. To provide ongoing support, advice and information to patients/volunteers with regard to their participation in clinical research. To undertake home visits when necessary to engage with and recruit service users to research projects. To cover duties of other AHPs/ RNs/ RDU staff when required. Be willing to engage in flexible working hours to facilitate study visits. To attend Investigator Meetings where applicable, and/or to attend project management group meetings for specific research projects which may, on occasion, involve travelling outside the region. Attendance at site selection or monitoring visits may also be required.