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.