Please review job description for further details. Duties will also include; Identification of patients who are suitable for entry into clinical trials and plan the care and support of patients according to clinical trial protocols, and to monitor responses throughout the trial Communicate with other research nurse and co-ordinators within the Trust and develop good working relations to help support them where necessary and encourage a good working relationship with the medical doctors and nurses involved in patient care and facilitate a team approach to patient recruitment/enrolment to trials and safe practice. Work at all times according to regulations as described in ICH, Good Clinical Practice (GCP), and to the most current guidance relating to research governance and research ethics in each Trust and liaise with Clinical Trial Offices and external investigators and designated staff within supporting departments when necessary to set up and coordinate research studies. Support the research strategy of the Trust. To view the main responsibility, please see the attached the Job Description and Person Specification.