The post holder will: Lead on participant communications and well-being issues,providing specialist advice relevant to clinical research nursing Be responsible for leading aresearch nurse team to support screening of eligible research participants including providing information and support to participants, clinical follow-up, data collection and safety reporting according to requirements Work with the CRF Matron toestablish and maintain key strategic relationships with networks of clinicians, researchers and health service managers for effective roll-out of thetrial Work alongside a team oftrial coordinators, data managers and database developers to ensurecompliance withGCP,dataprotection and research governance frameworks, regulations and sponsorrequirements Supportthedevelopment of trainingmaterialsfor clinical research staff at study sites including study specific and informed consent training and elements of GCP Monitor participants experience and identify importantparticipantswell-beingissues Be a central point of contact for site staff for trial-specific procedures including support to participants, eligibility assessment, informed consent, and sample management.