Start Date
Immediate
Expiry Date
17 Sep, 25
Salary
44962.0
Posted On
17 Jun, 25
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Pharmaceutical Companies, Trial Practice, Teaching, Edge, Communications, Research, Clinical Trials, Training
Industry
Pharmaceuticals
Feasibility and Study set-up - Contribute to the set-up of research studies within the wider research team. Liaise with the R&I Professional Services Team, Principal Investigators, support departments, and multidisciplinary teams to ensure a thorough feasibility process - Able to identify and plan strategies for recruiting patients into trials. Working with Principal Investigators to develop initiatives to increase patient involvement. - Ensure trial protocols are followed and that trials are conducted according to the national research legislation, Research Governance Framework, R&I Standard Operating Procedures, GHNHFT policies and Good Clinical Practice.
Provide continuity of care for patients and carers throughout the trial programme. Receive informed consent and provide ongoing information, education and support to clinical trial patients and their carers. - Ensure trial records are accurately maintained, including, but not limited to: records in nursing/medical paper and electronic notes, case report forms, trial site files. Ensure that trust procedures and policies are followed and in accordance with Good Clinical Practice and R&I SOPs.
Responsible for ensuring accurate study records are maintained on EDGE (Clinical Trials IT system). Other Duties - Take an active role in research promotion for staff and patients. Provide teaching on clinical trials to healthcare professionals assist with educating patients and relatives about clinical trials and assist with the induction and education of new team members. To raise the profile of research and deliver research education days to members of the public.
Line management; coordinating the team, delegating duties and supporting their personal and practice development. This includes annual and performance management where necessary. - Work closely with the Lead Research Nurse/Coordinator and Research Matrons, and the Governance & Oversight Group to monitor performance and ensure research is conducted according to current regulations. - Take responsibility for recruiting and retaining team members in conjunction with the Lead Research Nurse/Coordinator.
Occasional community or home visits to patients. - Occasional lifting of boxes of A4 paper, A4 files and similar (up to 5kg) and transporting these to other sites - The post involves a combination of sitting and standing plus walking - There is a need to use a computer - Travel to other sites for meetings, training and education purposes. - Requirements to concentrate on information for long periods of time (e.g., concentrating for periods of time over an hour at a time when reviewing research applications or preparing reports). - 50% of time spent working in an open plan office - 50% of time spent working in clinical areas (talking to patients, taking blood, testing urine samples and administering some treatments
Responsible for ensuring accurate study records are maintained on EDGE (Clinical Trials IT system). Other Duties - Take an active role in research promotion for staff and patients. Provide teaching on clinical trials to healthcare professionals assist with educating patients and relatives about clinical trials and assist with the induction and education of new team members. To raise the profile of research and deliver research education days to members of the public.
Line management; coordinating the team, delegating duties and supporting their personal and practice development. This includes annual and performance management where necessary. - Work closely with the Lead Research Nurse/Coordinator and Research Matrons, and the Governance & Oversight Group to monitor performance and ensure research is conducted according to current regulations. - Take responsibility for recruiting and retaining team members in conjunction with the Lead Research Nurse/Coordinator.