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The position involves leading and participating in the development and validation of datasets, tables, listings, and figures (TLFs) that support the analysis and reporting of clinical trials. The role requires providing expertise for statistical programming activities and developing collaborative relationships within the Statistical Programming team, cross-functional teams, and external vendors. Core responsibilities include creating SAS programs to generate derived analysis datasets and content for TLFs, performing programming validation to ensure quality, providing programming support for project teams, leading submission preparations, reviewing key planning documents, interacting with vendors, ensuring quality of deliverables, identifying opportunities for increased efficiency, leading programming assignments, participating in process improvement initiatives, collaborating with other function managers, and developing training manuals for the Clinical Programming Group. The position may require up to 10% domestic travel to client sites and professional meetings.
