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CDARS/Standard Lead – Any US location – ICON plc – North Wales, PA | – 2-12-2014

Reporting Standards LeadThe Reporting Standards lead will work in the company’s Global Biostatistics & Programming organization and function as the manager responsible for defining, implementing and managing compliance regarding ICON data collection and reporting standards. Scope of roleFunctional domain scope: Statistical programming, statistics, data managementScope of activities: Study reporting related activities for [initially]the Pfizer account; management of standards and processes for clinical trial subject data collection and reportingPrimary dutiesEstablish and lead a governance and management framework within ICON for definition, management and maintenance of programming standards and standard codeDrive close partnership across relevant ICON functional domains to manage and support standards for end to end clinical trial data flowDevelopment and maintenance of standard library of data modules, tools and code for end to end clinical trial data flowDevelopment and management of change control process (including associated business processes and documentation)Definition and maintenance of ICON programming best practicesDefinition and maintenance of standard macro code structures / hierarchies / code naming conventions etc.Definition and management of programming operational standardsDefinition, measurement and reporting of programming standards compliance…                                                                

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