Manager, Statistical Programming

Role: Manager of Statistical Programming leading activities in early pharmaceutical development, focusing on a specific compound, indication, or therapeutic area. Responsibilities: oversee statistical programming tasks including development of SAS programs for ADaM data sets, Tables, Listings, Figures, and regulatory documentation; lead a team of programmers, manage resource planning, ensure quality and timely deliverables; develop standards and SOPs; mentor staff; interface with cross-functional teams such as Statistics, Data Sciences, Medical Writing, and Regulatory. Requirements: MS in Statistics, Computer Science, or related field with 8+ years, or BS with 10+ years relevant experience; proven leadership in statistical programming; expert knowledge of SAS, CDISC standards, drug development processes, and regulatory filings. HighValue: early-phase drug development, SAS, CDISC, regulatory submissions, team leadership. WorkSetup: not specified; no travel indicated.