Take the lead on delegated studies being responsible for their development, implementation and progress, co-ordinating clinical team responses and ensuring that studies are run in accordance with Good Clinical Practice guidelines and the Research Governance Framework Demonstrates expert communication skills throughout the research process to assess eligibility and provide on-going advice and information to participants with regard to their participation in research in order to facilitate effective informed consent Ensure appropriate and effective communication with all nursing, medical, paramedical and research staff and other external agencies Provide advice and support to other members of the multidisciplinary team with regard to ICH GCP, ethics approval and amendments, study set up, delivery and completion Ensure planning and organisation of complex activities across a range of studies requiring collaboration with other professionals and agencies. Promote and collaborate in developing good working relationships, maintaining good communication systems with departments to ensure that participants have an effective and efficient research experience Contribute to clinical and research governance processes including adverse event/incident reporting collaborating with any investigations and management of these Be actively involved in promoting the work of the research and development department. Act as a role model, presenting a positive image of self, team and the organisation Set, monitor, and maintain standards of care to improve the patient experience and outcome of care. Be responsible for the delivery and co-ordination of care, through appropriate professional practice, delegation and supervision of duties carried out by junior staff Promote equality in care and practice by recognising, respecting and meeting the needs and choices of individuals To participate in education and training of junior staff