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Senior Scientist, Methodology Research, Biostatistics
Strategic planning for, documentation of, and implementation of open-source software in a regulated pharmaceutical development environment.
Works with statistics and programming teams to ensure underlying information technology supports advanced analytics application needs.
Rapid response to implement/validate design, analysis, and simulation of clinical trials as needed by clinical trial teams.
Collaborates with statistical programming staff to ensure that all tools meet analysis requirements, internal standard operating procedures, and external regulatory requirements.
Prepares oral and written reports to effectively communicate development needs and results of analyses to cross-functional teams.
Ph.D. or equivalent degree in statistics/biostatistics/computer science/data science or related discipline, or a Master’s degree with a minimum of 3 years of relevant experience.