Clinical Research Delivery Nurse


Company:	NHS Jobs
Salary:	£39,959 to £48,117 a year
Hours:	Full-time
Location:	Oxford, OX3 9DU
Job type:	Contract
Posting date:	19 Oct 2026
Closing date:	2 Nov 2026

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Summary

Clinical Research Delivery The post holder will practice with knowledge, skills and behaviours to: Be responsible for assessment, planning, implementation, and evaluation of patient care during participation in clinical research visits.Manage workload and co-ordinate allocated clinical trials and research studies Assessing, planning & implementing care for clinical trial participants during research visits Practice in compliance with their code of professional conduct, being responsible and accountable for their decisions, actions, or omissions. Utilise effective communication skills through a variety of methods, supporting participants in decision making in relation to clinical trial and study entry and participation. Utilise effective communication skills with colleagues both internally and/or externally, in verbal, non-verbal and written communication methods, adapting to changing parameters as required, which includes thorough accurate documentation in patient records as required Provide and receive highly sensitive, complex or contentious information relating to participant involvement and care, and communicates information to participants, families or carers with respect, compassion and empathy Able to competently perform a range of clinical procedures as required as part of the research protocol, ensuring accurate data capture. Participate in and ensure compliance with Informed Consent Procedures, acting within boundaries of own competency, research regulation and Trust policies/SOPs. Participate in processing samples, in line with protocol and laboratory manuals as required, including handling dry ice and liquid nitrogen when trained. Use own professional judgment identifying when to escalate and seek senior support/guidance Support the research team with all administrative tasks, including study set up including completion of feasibility requests, as required Ensure all necessary regulatory approvals are in place prior to approaching potential study participants Work within the limits of the approved protocol and any approved amendments To act as a participant advocate Please see more on JD and PS

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