We currently are seeking a dynamic, strategic, and innovative Sr. Statistician. This key position will be based in our corporate offices located in Northridge, CA (So. CA).
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.
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.
Career Site - Self Service
Masters or Ph.D in statistics, biostatistics, or related field.
Eight or more years of research in data analysis and/or statistician experience.
Proven experience performing complex statistical programming and statistical analysis and systems programming.
Strong SAS programming skills (Proficient in BASE, STAT, MACRO and GRAPH).
Demonstrated proficiency in using Microsoft Excel, SAS and/or STATA (statistical software), which includes data access, data retrieval, data management, data analysis, and data presentation.
Experience with a wide variety of clinical trials/designs and corresponding reporting of data, and large-scale multivariate longitudinal databases.
Experience in interpreting the results of statistical analyses from complex data sets.
Pharmavite is proud to be an equal opportunity and affirmative action employer. F/M/Disability/Vet
For more than 45 years, Pharmavite has been a trusted leader in the wellness industry, recognized for providing quality vitamins, minerals and supplements under our Nature Made® brand name.
Who We Are: Our mission is People creating new products for better health worldwide.
What We Do: Our vision is inspiring the healthiest you through more complete nutrition... Wherever you are in life.
As a member of the Pharmavite team, employees enjoy competitive salaries and an exceptional benefits package which includes medical, dental, vision, 401K, life insurance, and long term disability coverage. In addition, all employees enjoy our bonus program, educational assistance, credit union membership, substantial discounts on our products, 11 paid holidays per year, and an opportunity to be part of a health/wellness organization.