Highly motivated, results‐oriented, professional with strong analytical and problem-solving abilities, project management capabilities, and interpersonal communication skills. Experience in designing pre-clinical laboratory studies, as well as dose-finding Phase 1/1b studies, single-arm or randomized Phase 2 studies, and larger randomized Phase 3 studies that include correlative biologic endpoints. Responsibilities include: power and sample size calculations, statistical analysis plans, production of randomization tables, participation in the development of forms for electronic data capture, and all required analyses to address study objectives.