I am passionate about pursuing projects to improve the safety and efficacy of clinical trials. My work in the Integrated Evidence Statistical Innovation Group is focused on creating analytical approaches to improve the efficiency and rigor of clinical trials, centered on the use of external controls.I received a MS in biostatistics from Harvard University and a PhD in clinical science from the University of Colorado, where I am also an instructor on ethics and the responsible conduct of research. Specialties: biostatistics, external control arms, synthetic control arms, FDA/ICH regulations, oncology, drug and medical device clinical trials, propensity score methods, machine learning, postmarket surveillance natural language processing/NLP, risked based monitoring, risked based quality management, software system development, CRF/eCRF design/system validation.
Listed skills include Fda, Lifesciences, Clinical Research, Quality Assurance, and 25 others.