Aparna Anderson, Ph.D., joined Statistics Collaborative, Inc. (StatCollab) in 2016. She has extensive experience as a clinical trialist across a range of therapeutic areas. Prior to joining StatCollab, she worked at Bristol-Myers Squibb Company (BMS) from 1997 to 2016 and was an Assistant Professor in the Division of Biostatistics at the University of Minnesota from 1995 to 1997. She serves on the Executive Committee At Large for the American Statistical Association Section on Statistical Consulting from 2020 to 2022.
For more than twenty years, Dr. Anderson has contributed to clinical trial design, interpretation of trial results, conference presentations and manuscripts, diagnostic development, and health authority interactions. She has brought statistical and scientific perspectives to pipeline strategy, including proof-of-concept transition product development, due diligence for in-licensing and acquisitions, go/no-go decision-making, and Phase 3 trial design. She has interacted with regulators (e.g., FDA, EMA, and Health Canada) for end-of-Phase 2 and development discussions, pre- and post-submission meetings, and advisory committee presentations.
During her tenure at BMS, Dr. Anderson provided statistical leadership for the clinical development of ipilimumab and nivolumab, two pioneering therapies in the field of immuno-oncology. Her contributions to the ipilimumab melanoma trial designs resulted in global approvals for first- and second-line metastatic melanoma as well as adjuvant melanoma. During this period, she also helped to define alternative response criteria to address response kinetics unique to immuno-oncology agents. For her contributions as the lead nivolumab statistician between 2011 and 2016, BMS recognized Dr. Anderson in 2016 with the James B. D. Palmer Award for Excellence in Drug Development.
Dr. Anderson has contributed to clinical development in numerous therapeutic areas in addition to oncology including rare diseases, neuroscience, pediatric indications, metabolic diseases, infectious diseases, and cardiovascular diseases. She has contributed to clinical components of Common Technical Documents, including statistical analysis plans and data set submission plans. She sits on multiple data monitoring committees (DMCs) to provide patient safety monitoring and interpretation of interim efficacy analyses in clinical studies. She has also served as an expert witness in litigations.
While at the University of Minnesota, she taught courses in multiple linear regression and longitudinal data analysis, collaborated in grant submissions at the Center on Aging, and was part of an advisory panel for violence prevention grant-based research.
Dr. Anderson received a B.S. in Applied Mathematics from the University of California, Davis (1989) and her M.S. and Ph.D. in Biostatistics from the University of Washington (1995). In 1989 to 1990, she spent a year studying mathematics as a Fulbright scholar at the University of Göttingen, Federal Republic of Germany.
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