Clinical Research Nurse

For further information on this role, please see the attached detailed

Job Description and Person Specification

To coordinate arrangements required for patients undergoing specialist investigations as part of the research protocol. To assess the patient prior to trial treatment, monitor the patient receiving trial treatment and follow the patient up on completion of trial treatment as required by protocol. To collect and accurately record data in accordance with requirements of the trial protocol. To participate in the design and preparation of research protocols, patient information sheets and other documentation associated with clinical trials, ensuring that these are reviewed and updated as required. To safeguard the integrity of the trial by ensuring compliance with ICH GCP guidelines. To be involved with the running of several concurrent research studies.