non title Oxford, England
Job description
Ensure accurate complex data administration and entry for allocated clinical trials. Assist in the ongoing development and maintenance of multi-access trial databases as necessary. Where appropriate, submission of appropriate documentation to relevant authorities including REC and liaising with Research and Development Department Liaise with the research team to accurately record trial data in various trial databases in accordance with the principles of the ICH Good Clinical Practice. Maintain accurate record keeping Assist with trial monitoring and close out visits Assist with project work undertaken in the department Help organise and attend trial Site Initiation Visits Create trial work sheets as necessary and ensure patient packs are kept up-to-date and readily available for use by the clinical team
