Research Nurse
| Dyddiad hysbysebu: | 10 Tachwedd 2025 |
|---|---|
| Cyflog: | £38,383.00 i £46,205.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £38383.00 - £46205.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 16 Tachwedd 2025 |
| Lleoliad: | Bristol, BS34 5TF |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | A0219-25-0045 |
Crynodeb
Working collaboratively with the wider research team, you will support the safe and effective conduct of a variety of clinical studies, including commercial studies and those adopted to the NIHR Portfolio. All activities will be carried out in accordance with relevant regulatory and legal frameworks governing the planning, execution, and closure of clinical research. You will work closely with the Administration Officer(s) to ensure that site files are maintained to a high standard and remain compliant. Additionally, you will be responsible for ensuring that studies are delivered on time and in alignment with agreed targets. The post-holder will develop good working relationships with: Research team Wider practice team Patients participating in clinical research External clinical trial sponsors and providers Clinical Responsibilities Undertake a variety of delegated duties in accordance with the guidelines and protocols set by the Surgery and individual studies being conducted. Assess patients suitability for participation in studies and ensure informed consent is appropriately obtained. Coordinate logistics for patient visits and perform patient assessments as outlined in study protocols, including blood collection and centrifugation. Conduct required screening procedures in line with study criteria. Competently interpret clinical records, charts, and care documentation to assess clinical interventions, medications, and patient responses, ensuring suitability for inclusion in individual trials. Accurately record all research activity to maintain clear and contemporaneous study documentation, including the reporting of adverse and serious adverse events. Ensure compliance with ICH-GCP, ISO 14155, and all relevant local, national, and international legislation, proactively identifying and addressing any incomplete, inaccurate, or misleading documentation. Other Responsibilities within the Organisation: Assist in the overall setting up, organisation and running of a clinical trial within the practice to Good Clinical Practice (GCP) guidelines within the Research Governance framework and adhering to other related regulations/SOPs. Co-ordinate arrangements for patients participating in clinical trials, according to study protocols, and communicate all necessary information to relevant personnel. Take day to day responsibility for the management of a portfolio of trials relating to site specific area(s), ensuring that information is kept up to date and a comprehensive portfolio is maintained as far as possible by working closely with investigators. Provide leadership and motivation for staff, facilitating orientation and training programs, ensuring information about studies is available and disseminated as appropriate. Undertake any other duties commensurate with the post holders grade as agreed with the principal investigator or management team.