{"interviewQueryText":"What are some good interview questions in British English for the job description below?\n\n-------------------------------------------\n\nResearch Nurse with Cwm Taf Morgannwg University Health Board in Merthyr Tydfil\n\n The post holder will be involved in ensuring that any research undertaken within the University Health Board safeguards the well being of the research participants, to include patients, staff and control subjects. This will involve supporting participants through the research pathway, in accordance with the research protocol and relevant legislation. . The postholder will support the Assistant Director for R&D and the R&D Manager in meeting the Research and Development Division, Welsh Government Key Performance Indicators and Metrics. Working as part of a well established team, the post holder will be involved in ensuring that any research undertaken within the University Health Board safeguards the well being of the research participants, to include patients, staff and control subjects. This will involve supporting participants through the research pathway, in accordance with the research protocol and relevant legislation. We are seeking to appoint a highly motivated and well organised individual with a passion for research and a keen interest in developing and supporting collaborative commercial and non commercial research within the University Health Board. The post holder will be working as part of a well established team of research nurses, officers and assistants to support the set up and delivery of research across the UHB. The ability to speak Welsh is desirable for this post; Welsh and/or English speakers are equally welcome to apply. About us You will be able to find a full Job description and Person Specification attached within the supporting documents or please click Apply now to view in Trac The post holder will be required to identify and screen study participants, in accordance with the research protocol and in conjunction with members of the research team. The post holder will provide specialist advice and guidance on the research process to potential participants, to ensure that they fully understand the nature of the study and protocol pathway, enabling valid informed consent. The post holder will take informed consent from study participants, in line with ICH Good Clinical Practice guidelines. The post holder will support patients through the research pathway for approved commercial and non-commercial research projects, ensuring that patient safety is paramount at all times. The post holder will be responsible for assessing feasibility, study set- up, support , coordination and operational management of commercial and non-commercial research studies across the University Health Board. The post holder will be required to undertake clinical procedures (eg. phlebotomy, questionnaire completion) on research participants as required. "}