- To assist the clinicians in the assessment of patients/volunteers for eligibility forresearch and monitoring of their condition throughout their participation.
- To provide ongoing advice and information to patients/volunteers with regard totheir participation in clinical research in order to facilitate effective informedconsent.
- To assist the clinicians to report and record any adverse events as dictated byTrust and Departmental protocols.
- To assist the clinicians with protocol development and ethical approval.
- To assist in the analysis of data and preparation of reports for presentation andpublication.
- To co-ordinate and carry out patient visits in accordance with study protocols,including co-ordinating special tests in other departments, collection of data, coding,data entry and patient support
- To carry out treatment procedures and treatment interventions according to predeterminedprotocols, including venepuncture, venous cannulation, administering ofintra-venous drugs and vital sign recording
- To report on a regular basis to the Senior Nurse of the R&D; department forprofessional support and guidance.
- To ensure that all clinical research activity is ICH GCP compliant and conducted inaccordance with the agreed protocols
- To maintain a high standard of patient care in line with Trust and R&D; policies andprotocols and in accordance with the Research Governance Framework
- To ensure that all data is collected and managed accurately
- To carry out the collection,



processing and shipping of biological specimensaccording to protocol requirements and follow up appropriately on alert values
- To be involved in the education of patients and their various aspects of their disease
- To ensure that patient safety is paramount in all procedures that take place for trialpurposes
- To ensure clinical and research documentation and record keeping is completedaccurately and efficiently in accordance with the EU Directive, ICH GCPGuidelines.
- To work within the N.M.C Code Of Conduct and scope of professional conduct
- To have sufficient computer skills for the handling and management ofcomputerised data
- To keep up to date with relevant medical literature, developments in clinicalresearch methodology, monitoring and local regulatory and ethical requirements
- To attend research network meetings, attend courses, conferences and study days in order to remain up to date with all relevant aspects of clinical research
- To participate in the education and development of staff/students, e.g. clinicalsupervision and ensure that all personnel are adequately informed about, andcomply with all details of the trials.
- To participate in the education and development of student nurses.
- The post holder will be expected to work clinical shifts in a ward setting ifnecessary

Liverpool University Hospitals NHS Foundation Trust

Liverpool University Hospitals NHS Foundation Trust

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📌 Research Nurse (Liverpool)
🏢 NHS Jobs
📍 Liverpool