Manager, Statistical Programming

Role: Statistical Programmer supporting biopharma clinical studies in neuroendocrine disease. Responsibilities include developing, validating, and maintaining analysis datasets, tables, listings, and figures for study reports and regulatory submissions; collaborating with Biostatistics, Data Management, Clinical Development, and external vendors; ensuring compliance with CDISC standards and regulatory requirements. The role may also involve study oversight, process improvement, and mentoring, depending on experience. Qualifications: MS in Statistics, Biostatistics, Mathematics, or related; 3-5 years of SAS programming experience in biotech/pharma/CRO settings; expertise in SAS, CDISC standards (SDTM, ADaM), and clinical trial reporting; ability to manage priorities independently; vendor oversight experience preferred for senior levels. High-Value: support for neuroendocrine clinical development, regulatory submission readiness, CDISC compliance, cross-functional collaboration, and vendor oversight. Work Setup: based in Boston, hybrid work model, with some travel expected.