Research Governance Officers coordinate management of applications for site authorisation to proceed with your study, and oversight of authorised research projects. They are also available to provide important advice and support in the pre-authorisation period.
Will your clinical trial need access within your hospital or facility to patients, staff or facilities? If yes, then you should liaise with your Research Office and any supporting departments in your organisation for information on any procedures including Access Request Review required for access to patients, tissue or data.