Position: Principal Statistical Programmer
, Manchester United Kingdom
Duties: Perform, plan co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically; Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies; Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies
Requirements: Minimum of 8+ years of experience in Statistical Programming in pharmaceutical or medical devices industry; Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results; Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes; Thorough understanding of relational database components and theory; Must have excellent knowledge of CDISC standards (SDTM andADaM)
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