Project leadership of assigned studies; Assign tasks to team members and provide oversight of their work; Work cross-functionally with other clinical team members; Negotiate timelines and scope of work; Work and make decisions independently; Manipulation of data to produce analysis datasets, including SDTM and ADaM datasets; Production and review of Tables, Figures and Listings (TFLs) according to statistical analysis plans; Creation and review of programming specifications and, if required, annotation of case report forms (CRFs) to CDISC standards
Requirements:
Bsc, MSc or PhD in mathematics, science or IT related discipline; Experience working within a clinical trials environment; Substantial experience working with SAS; CDISC (SDTM and ADaM) experience; Previous experience of leading teams is preferred but not essential; Excellent written and verbal communication skills
Text:
Senior Statistical Programmer Project leadership of assigned studies; Assign tasks to team members and provide oversight of their work; Work cross-functionally with other clinical team members; Negotiate timelines and scope of work; Work and make decisions independently; Manipulation of data to produce analysis datasets, including SDTM and ADaM datasets; Production and review of Tables, Figures and Listings (TFLs) according to statistical analysis plans; Creation and review of programming specifications and, if required, annotation of case report forms (CRFs) to CDISC standards Bsc, MSc or PhD in mathematics, science or IT related discipline; Experience working within a clinical trials environment; Substantial experience working with SAS; CDISC (SDTM and ADaM) experience; Previous experience of leading teams is preferred but not essential; Excellent written and verbal communication skills
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