Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers, Data Scientists, Dev Systems, and other Clinical, Global Drug Safety, Regulatory, IT, and Project Management staff to deliver on cross-functional initiatives and projects; Research and support the implementation of innovative trial designs by exploring statistical methodologies, understanding industry best practices, sharing knowledge with cross-functional teams, and supporting the design of innovative trials; Serve as a statistical expert for risk-based quality management, with a focus on developing centralized statistical monitoring methods, tools, and processes; Design, prototype, and build tools to empower study teams including analytical dashboards, trial simulation packages, data visualizations, and automated workflows
Requirements:
8+ years of industry experience in clinical trials and a BS degree in Biostatistics or equivalent; Strong background in statistics, programming, and data analysis; Hands-on trial statistician experience with trial design, conduct, analysis, and reporting; Deep and broad knowledge of current statistical methods and drug development best practices; Expert in R and Python including experience with statistical simulations, package and Shiny development, and machine learning or AI-related use cases
Text:
Sr. Manager, Biostatistics Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers, Data Scientists, Dev Systems, and other Clinical, Global Drug Safety, Regulatory, IT, and Project Management staff to deliver on cross-functional initiatives and projects; Research and support the implementation of innovative trial designs by exploring statistical methodologies, understanding industry best practices, sharing knowledge with cross-functional teams, and supporting the design of innovative trials; Serve as a statistical expert for risk-based quality management, with a focus on developing centralized statistical monitoring methods, tools, and processes; Design, prototype, and build tools to empower study teams including analytical dashboards, trial simulation packages, data visualizations, and automated workflows 8+ years of industry experience in clinical trials and a BS degree in Biostatistics or equivalent; Strong background in statistics, programming, and data analysis; Hands-on trial statistician experience with trial design, conduct, analysis, and reporting; Deep and broad knowledge of current statistical methods and drug development best practices; Expert in R and Python including experience with statistical simulations, package and Shiny development, and machine learning or AI-related use cases
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