Research Nurse
| Dyddiad hysbysebu: | 02 Gorffennaf 2025 |
|---|---|
| Cyflog: | £37,335 i £44,962 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £37335 - £44962 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 16 Gorffennaf 2025 |
| Lleoliad: | Newcastle upon Tyne, NE3 3PF |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | B0084-25-0018 |
Crynodeb
The following are the core responsibilities of the Research Nurse. There may be, on occasion, a requirement to carry out other tasks; this will be dependent upon factors such as workload and staffing levels. a. Deliver high quality of clinical care, incorporating excellent communication skills, and an understanding of the regulatory and legal frameworks related to the planning, recruitment, and follow-up of clinical research in relation to the safe conduct of research. b. Ensure that all trial procedures including identifying potential participants for recruitment and providing verbal and written information to explain studies to potential participants are conducted in accordance with ICH Good Clinical Practice (GCP) UK Policy Framework for Health and Social Care Research as well as all other relevant legislation. c. Complete study specific procedures such as venepuncture, ECG, and support investigations according to study protocols and within the scope of their practice and competency. d. Provide administrative and data management support for all aspects of trial coordination and organisation. e. Be responsible for implementing, assessing, and managing the care pathways for clinical research participants and their carers with Principal Investigator (PI) oversight. This will involve the correct identification and recruitment of eligible participants, education, training and monitoring of trial participation and the timely collection and documentation of accurate data. f. Review searches against study specific criteria in order to identify patients who might be suitable to be considered for study participation. g. Consent patients into clinical research trials. h. Provide ongoing advice and information to participants with regard to their participation in research in order to facilitate effective informed consent. i. Act as point of contact for research participants before, during and after study participation. j. Complete follow up visits as indicated in study specific schedule of events. k. Clear and effective communication with both internal and external stakeholders as well as secondary care organisations, GP practices, patients, and carers. l. Be able to provide participants with information, which may be complex or sensitive regarding their participation in clinical research and the care they receive subsequently as a consequence. m. Co-ordinate the safe collection, transfer, and storage of blood/tissue samples in accordance with the Human Tissue Act 2004 and as required by each study specific trial protocol. n. Oversee maintenance of investigator site files and essential documentation in accordance with ICH-GCP and NGPS standard operating procedures to ensure that they are kept inspection ready at all times.