Senior Scientist, Statistical Programming

Role: Senior Scientist in Statistical Programming supporting late-stage drug/vaccine clinical development, focusing on analysis, reporting, and dataset design for regulatory submissions and post-marketing. Responsibilities include developing statistical analysis datasets, ensuring process compliance, collaborating with cross-functional teams, and serving as a project lead across multiple projects. Requirements: Master’s degree in a related field plus 3 years or Bachelor’s plus 5 years SAS programming experience in clinical trials; expertise in CDISC ADaM standards, SAS, data systems, and clinical data concepts. Preferred: experience in R&D analysis/deliverables, statistical methodologies, and project leadership. High-Value: involvement with clinical development in pharmaceutical or vaccine areas, supporting late-stage (Phases 3 or post-marketing) projects, with strong emphasis on regulatory compliance, data standards, and global health impact. Work setup: not specified, but typical for senior roles; no travel or remote details provided.