Position Summary:

Provides senior-level oversight of statistical aspects in the design of clinical trials and statistical analysis of analytical and clinical trial results. Collaborates with the Science & Technology, Analytical Research Services, Regulatory Affairs, and Quality organizations to provide in-depth expertise in the statistical evaluation and publication of clinical study reports, analysis of stability studies, among other things.

Responsibilities:

• Analyze and assist in the interpretation data from clinical trials, stability or analytical testing, publicly available metadata, research information relevant to nutrition science and the dietary supplement industry (e.g., NHANES), or work product created by Pharmavite's Science & Technology, Analytical Research Services, Regulatory Affairs, and Quality (STARQ) organizations.
• Develops, plans and executes a wide range of statistical analyses including multi-variable, mathematical modeling, power and sample size calculations, among other things.
• Synthesize and simplify complex information to develop business strategies or to influence key opinion leaders and industry experts; at scientific conferences or industry events; or in peer-reviewed manuscripts.
• Collect and analyze data to develop and maintain STARQ metrics.
• Functions as analytics expert for multiple complex projects and coordinate with other data analytics incumbents in the Supply Chain.
• Designs, maintains and documents procedures, including methods and summary/conclusions.
• Ensure that appropriate programs and documentations are developed for datasets development and outputs generation, and ensure the statistical analyses specified in scientific protocols and/or analysis plans are conducted appropriately.
• Collaborate with members of the STARQ community and other functions on clinical study protocol development, including choosing an appropriate study design and statistical methodology, defining endpoints, calculating sample size, and writing statistical sections of the protocol.
• Collaborate with members of the STARTQ community and other functions on documents containing statistical information and clinical data.
• Contribute to the development of functional-level standards, SOPs, and templates.