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Leading on development of data capture tools, creation of metadata, database testing, data query management and quality control. Other duties include development of trial documentation in accordance with trial protocols and unit guidelines. Additional tasks include maintaining a trial master file and trial delegation logs, data entry, assisting with trial site budgets, developing materials and agendas for team meetings, international meetings, clinical endpoint review meetings and minute taking. The role also involves providing training, information and advice to trial clinicians, research nurses and pharmacists on data capture, operational procedures and database functionality. These tasks are also to be undertaken as part of a site initiation visits at international sites.
Administrative support to trial teams, senior scientific staff, statisticians, clinicians and trial managers. Duties included processing of confidential information, arranging travel and accommodation, organising meetings and events, minute taking, monitoring web based teleconferences, arranging couriers, processing expenses and raising requisitions for purchases and invoice payments.
CPE in Law