Clinical Research Practitioners (CRPs) are crucial to delivering clinical research that is transforming treatment in the NHS and the care wereceive. CRPs bring a wealth of research knowledge and expertise to research delivery teams, working alongside nurses and others to deliversafe, ethical and high quality clinical research care. The post-holder will be responsible for supporting studies from set up through to the completion of the follow up phase and for overseeing and/or managing single site studies as required. To support current research staff in ensuring the completeness, accuracy and consistency of the data in order to meet standards expected forreporting to regulatory bodies, by organising and managing study days. To provide clinical support and supervision to patients in clinical trials such as the taking of informed consent, taking samples, performing testsand physical measurements and preparing and maintaining study documentation, in accordance with the clinical trial protocol and Good ClinicalPractice. (Please refer to the job description/person specification for further details on the role)