Research Nurse


Company:	NHS Jobs
Salary:	£39,959 - £48,117
Hours:	Full-time
Location:	Bristol, BS2 8ED
Job type:	Permanent
Posting date:	30 Jul 2026
Closing date:	13 Aug 2026

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Summary

Clinical Trial Coordination Take daytoday responsibility for coordinating a portfolio of clinical trials, ensuring compliance with all regulatory and governance standards including ICHGCP and Trust SOPs. Work collaboratively with investigators, clinicians and the wider Clinical Trials Unit to maintain accurate, uptodate trial information and ensure safe, efficient trial delivery. Patient Care & Clinical Responsibilities Assess and monitor patients throughout their trial participation, documenting outcomes, adverse events and relevant clinical observations. Administer investigational and standard treatments, including cytotoxic chemotherapy (training and competency support available). Act as a consistent point of contact for patients and carers, providing clear information and maintaining a patientcentred approach. Attend relevant clinics, MDTs and ward rounds to promote continuity of care and facilitate safe trial delivery. Trial Procedures & Data Quality Undertake venepuncture, sample handling, spinning, storage and transport according to study protocols. Ensure all data is collected accurately, promptly and in accordance with study requirements. Contribute to trial setup, including reviewing protocols, supporting ethics/R&D processes and preparing study documentation. Leadership, Training & Team Support Provide leadership, guidance and motivation to staff involved in research delivery. Support teaching programmes, training, and induction of colleagues across the Division. Deputise for Senior Research Nurses as required and support the strategic development of the Clinical Trials Unit. Participate in audits, quality improvement projects and divisional research initiatives. Additional Responsibilities Act as a link nurse (e.g. health & safety, manual handling) as required. Work flexibly across Bristol and Weston to support research throughout the cancer pathway. Attend studyrelated meetings and training locally, nationally or internationally. Maintain compliance with Trust policies on safeguarding, information governance, health and safety, and clinical governance.

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