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Description
Clinical Responsibilities: to include level of responsibility for: Prepare patient information sheets and consent forms concerning trials Organise the packaging and shipment of diagnostic samples Maintain spreadsheets/databases on patient recruitment. Responsible for updating all information pertaining to trials in order to ensure that patients are in receipt of the correct information prior to entry into any clinical trial programme. To support the safe conduct of research and to provide assurance that the rights, safety and well-being of trial participants (patients) are protected. Facilitate reporting of study adverse events to the trial centre and R&D Department.
To assist with the co-ordination of the patients journey through the clinical trial protocol e.g. requisition and organisation of any necessary investigations Please see attached job description for further information.
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