Clinical Trial Administrator

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

Job Description and Person Specification

To ensure that data collection and (electronic) case report form ((e)CRF) completion is performed to the required standards of the current EU, UK and FDA legislation, Trust SOPs and Sponsor contractual obligations. To design and implement tools and guidance for clinical trial data capture. To regularly report on data entry status to ensure deadlines are met for interim and final analysis. To represent the Data Management team at research meetings. To prepare and facilitate the archiving of essential clinical trial documents and source data as per Trust SOPs. To undertake projects with relation to office management as required. Tissue tracking using RMH systems (as applicable) Ensure that scans are uploaded to trial specific electronic portals where required.