Research Nurse
| Dyddiad hysbysebu: | 08 Hydref 2025 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | Negotiable |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 31 Hydref 2025 |
| Lleoliad: | Watford, WD18 7QR |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | A2717-25-0001 |
Crynodeb
This research nurse role combines clinical expertise with the coordination and management of research studies. The candidate will act as a central point of contact between patients, investigators, and regulatory authorities, ensuring all research is delivered safely, ethically, and to the highest standards in alliance with Good Clinical Practice guidelines. Clinical Responsibilities Assessing, screening, and recruiting suitable patients/participants for research studies providing ongoing review of clinical trial participants and the delivery of clinical investigations and treatments, as defined by the clinical trial protocol. Obtaining informed consent where appropriate, ensuring participants understand the study, risks, and rights. Performing clinical procedures such as blood sampling, administering study medications, monitoring vital signs, and managing and recording side effects. Manages the patient schedule to ensure all observations, interventions and procedures are carried out in accordance with the trial protocol Acting as a patient advocate, ensuring safety and wellbeing throughout the study. Ensuring compliance with ethical approvals, research governance, and legal requirements. Upholding confidentiality and data protection standards. Research & Administrative Responsibilities Ensuring strict adherence to research protocols, Good Clinical Practice (GCP), and ethical standards. Collecting, recording, and managing study data accurately and securely. Coordinating study visits, follow-ups, and assessments. Liaising with doctors, investigators, and multidisciplinary teams involved in the research. Reporting adverse events or complications promptly within the expected time frame. Data management, ensuring source data is recorded accurately and inputted into the electronic case report forms in a timely manner in accordance with the study protocol Maintaining research documentation. Works autonomously to co-ordinate different aspects of trial procedures. Responsible for ensuring all studies achieve recruitment targets and timelines. Responsible for assessing and evaluating any potential cost implications associated with clinical trials. Liaising with the practice manager, and other Research staff during feasibility process. Submitting Expressions of Interest to potential research sponsors. Work within the Standard Operating Procedures for Research, Good Clinical Practice and relevant clinical trial protocols. Education & Communication Educating participants and their families about the research process. Acting as a point of contact between patients, investigators, and external research bodies. Informing staff or other healthcare professionals about study procedures. Promoting awareness of clinical research within the healthcare setting. Ensuring your own training records are compliant and remain up to date in accordance with GCP