Duties: Undertake design and analysis of complex studies and provide statistical support, making contributions to clinical development plans. Utilize adaptive design and Bayesian methods, including trial simulation, to innovate and improve study design. Execute strategic, statistical thinking and guide the direction to improve the statistical methodology, processes, and delivery activities of study design. Responsible for analyzing, interpreting, summarizing, and presenting results of clinical trials. Develop design options and provide quantitative decision support and will oversee internal and external statisticians in the delivery of analysis and reporting on our clinical program designs
Requirements: Must possess a Master’s or foreign equivalent, in Statistics, Mathematics, or a related field, and five (5) years of experience in the job offered, as a Statistician, or in a related occupation. Must possess five (5) years of experience all of the following: Designing Phase III Oncology clinical trials including adaptive designs or through Bayesian methods; R, R-shiny and SAS programming; Conducting simulations; Performing biomarker analyses; Developing and submitting sNDA and NDA; Developing scientific publications of clinical oncology trials