Associate Principal Scientist, Statistical Programming

Role: Senior statistical programmer supporting late-stage drug/vaccine clinical development projects, responsible for developing and executing statistical analysis datasets, reports, and visualizations across multiple trials and regulatory submissions. Responsibilities include designing and maintaining datasets for clinical development, outcomes research, and safety evaluation; collaborating with stakeholders to ensure efficient project execution; serving as the primary programming contact throughout the project lifecycle; and leading global programming teams, including outsourced staff. Requirements: Bachelor's or Master’s degree in a relevant field with 7-9 years of experience; extensive expertise in SAS programming, clinical trial data management, CDISC/ADaM standards, and regulatory submission development; proven leadership in large/complex programming projects; and experience with U.S. and/or global regulatory submissions. Preferred skills include strong understanding of statistical models, terminology, and the ability to translate analysis strategies into tactical activities. HighValue: focus on pharmaceutical or vaccine development, late-stage clinical trials, regulatory deliverables, and global programming coordination. Work setup: full-time remote with approximately 10% domestic travel.