Support Medical Directors and Clinical Development in exploring and conducting novel analyses of existing clinical trial, natural history, and real-world data (e.g., post hoc, subgroup, and descriptive analyses), including helping frame analysis questions, coordinating with Biostatistics and Data Management, and summarizing results for internal review and scientific communications. Assist in identifying and evaluating data generation opportunities (e.g., investigator-initiated studies, registries, chart reviews, and real-world evidence collaborations) by supporting data gap assessments, preparing concept summaries, and coordinating cross-functional input, with prioritization and approval decisions remaining with Medical Affairs leadership.