Manager Statistical Programming

Role: Manager of Statistical Programming supporting clinical studies, responsible for delivering programming outputs from study initiation through regulatory approval and product launch. Responsibilities include leading table, listing, and graph development and quality control, managing project timelines, contributing as a programming representative on study teams, and supporting resource planning and team development. Requirements: Master's degree with 8-10 years' experience or relevant advanced degree with 5+ years' programming and project management in a regulated biopharma setting; proven leadership in clinical programming; strong organizational, documentation, and regulatory compliance skills. Preferred: SAS certification. High-Value: supporting a broad clinical portfolio, experience in regulated environments, leadership in cross-functional teams, onsite in Warren, NJ or Cambridge, MA, with no travel specified.