Research Nurse
| Posting date: | 27 February 2026 |
|---|---|
| Salary: | Not specified |
| Additional salary information: | Negotiable |
| Hours: | Full time |
| Closing date: | 03 March 2026 |
| Location: | London, W67HY |
| Company: | NHS Jobs |
| Job type: | Permanent |
| Job reference: | A3071-26-0000 |
Summary
Key Responsibilities Participant-Facing Responsibilities Act as a key contact for research participants and their families/carers, providing information, support, and reassurance throughout the study. Conduct telephone pre-screening and arrange screening visits. Obtain informed consent for study participation in line with ethical and regulatory standards. Undertake study-specific clinical assessments and procedures (e.g., venepuncture, ECGs, vital signs, sample processing, and drug administration). Monitor participants progress, safety, and well-being during and after study visits. Record and report adverse events and serious adverse events (SAEs) promptly and accurately. Clinical Trial Set-up Attend Study Initiation Visits and contribute to site set-up activities. Ensure readiness of facilities, equipment, and supplies for research delivery. Support development of site-specific documentation, including delegation logs and nursing SOPs. Contribute to the preparation and organisation of Investigator Site Files. Clinical Trial Delivery Register and recruit participants in line with study inclusion/exclusion criteria. Administer trial treatments according to study protocols and within scope of NMC practice. Accurately document clinical activities and research data in Case Report Forms (paper and electronic). Perform study-required sampling, storage, and shipment of biological specimens. Ensure compliance with GCP, the Research Governance Framework, Medicines for Human Use (Clinical Trials) Regulations, and local SOPs. Liaise with the NIHR Clinical Research Network and other stakeholders to support study delivery. Study Close-out Support the smooth transition of participants from research to conventional care pathways. Ensure resolution of outstanding data queries. Support archiving of study documentation in line with ICH-GCP and study agreements. Communication & Collaboration Communicate effectively with participants, carers, multidisciplinary teams, research staff, sponsors, and external collaborators. Provide regular updates to investigators and the Research Unit Manager on recruitment, trial progress, and any issues affecting delivery. Represent the Unit in local, national, and international research collaborations. Clinical Practice Communicate effectively with participants, carers, MDT colleagues, research teams and external collaborators. Maintain competency in emergency procedures and research-related clinical skills. Uphold high standards of infection control, medicines management, and patient safety. Promote equality, diversity, and patient-centred practice in all research activities. Education, Training & Research Maintain an up-to-date knowledge base in research legislation, governance, and GCP. Undertake mandatory training and role-specific professional development. Contribute to the training and supervision of junior staff, students, and Clinical Research Practitioners. Support audits, quality assurance activities, and dissemination of research findings. Leadership & Management Manage personal workload effectively, prioritising competing clinical and research demands. Support investigators and the research team in trial planning, organisation, and problem solving. Monitor and maintain adequate study supplies, equipment, and clinical materials. Contribute to inspections, audits, and continuous quality improvement initiatives. Liaise with investigators, sponsors, and external research bodies as appropriate. This list is not exhaustive