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Research Delivery Nurse

Job details
Posting date: 18 June 2024
Salary: £35,392.00 to £42,618.00 per year
Additional salary information: £35392.00 - £42618.00 a year
Hours: Full time
Closing date: 30 June 2024
Location: Oxford, OX3 7LE
Company: NHS Jobs
Job type: Contract
Job reference: C9321-24-1610

Summary

Main Tasks and ResponsibilitiesClinical ResearchThe post holder will practice with knowledge, skills and behaviours which Be responsible for assessment, planning, implementation, and evaluation of participant careduring 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 andaccountable for their decisions, actions, or omissions. Utilise effective communication skills through a variety of methods, supporting participants indecision 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 participants records as required Provide and receive highly sensitive, complex or contentious information relating to participantinvolvement and care, and communicates information to participants, families or carers withrespect, compassion and empathy Able to competently perform a range of clinical procedures as required as part of the researchprotocol, ensuring accurate data capture. Including: assisting with SARS-CoV-2 inoculations;collection, preparation and processing of biological samples; caring for and managing quarantineparticipants; assisting with participant pre-screening and screenings procedures; conductingClinical service lead:Research Matron (UO)Learning, Respect, Delivery, Excellence, Compassion, ImprovementResearch Nurse JD (DEC 2022)study follow-up visits Participate in and ensure compliance with Informed Consent Procedures, acting withinboundaries of own competency, research regulation and Trust policies/SOPs. 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 includingcompletion of feasibility requests, as required Ensure all necessary regulatory approvals are in place prior to approaching potential studyparticipants Work within the limits of the approved protocol and any approved amendments For more details, please see the Job Description.