Responsibilities Work with cross-functional teams to articulate drug development questions, assess feasibility of endpoints, and frame statistical approaches. Design clinical experiments and interventional studies to generate and analyze data. Interpret results and support program-level decision‐making. Co‐author clinical study protocols and statistical analysis plans; perform statistical analyses for interim and final reports. Develop and deliver training to non‐statistical colleagues. Collaborate on development of new infrastructure and processes. Influence external pharmaceutical/regulatory environment through professional associations, conferences, and publications. Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, and Medical Writing to design and analyze clinical trials. Determine appropriate statistical methodology; collaborate with Statistical Programming on tables, figures, and listin...