Research Nurse - Liverpool Heart and Chest Hospital

To assist the clinicians in the assessment of patients/volunteers for eligibility for research and monitoring of their condition throughout their participation. To provide ongoing advice and information to patients/volunteers with regard to their participation in clinical research in order to facilitate effective informed consent. To assist the clinicians to report and record any adverse events as dictated by Trust 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 and publication. 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 pre- determined protocols, including venepuncture, venous cannulation, administering of intra-venous drugs and vital sign recording To report on a regular basis to the Senior Nurse of the R&D department for professional support and guidance. To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with the agreed protocols To maintain a high standard of patient care in line with Trust and R&D policies and protocols 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 specimens according 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 trial purposes To ensure clinical and research documentation and record keeping is completed accurately and efficiently in accordance with the EU Directive, ICH GCP Guidelines. 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 of computerised data To keep up to date with relevant medical literature, developments in clinical research 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. clinical supervision and ensure that all personnel are adequately informed about, and comply 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 environment if necessary Job description Job responsibilities To assist the clinicians in the assessment of patients/volunteers for eligibility for research and monitoring of their condition throughout their participation. To provide ongoing advice and information to patients/volunteers with regard to their participation in clinical research in order to facilitate effective informed consent. To assist the clinicians to report and record any adverse events as dictated by Trust 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 and publication. 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 pre- determined protocols, including venepuncture, venous cannulation, administering of intra-venous drugs and vital sign recording To report on a regular basis to the Senior Nurse of the R&D department for professional support and guidance. To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with the agreed protocols To maintain a high standard of patient care in line with Trust and R&D policies and protocols 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 specimens according 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 trial purposes To ensure clinical and research documentation and record keeping is completed accurately and efficiently in accordance with the EU Directive, ICH GCP Guidelines. 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 of computerised data To keep up to date with relevant medical literature, developments in clinical research 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. clinical supervision and ensure that all personnel are adequately informed about, and comply 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 environment if necessary