Senior Manager Statistical Programming

Role: Senior Manager, Statistical Programming at Regeneron, providing technical leadership in statistical programming across multiple therapeutic areas within clinical development. Responsibilities: lead programming support for studies, ensure regulatory submission preparation, coordinate documentation, mentor team members, and contribute to departmental strategies. Collaborate globally with study teams and external vendors to deliver high-quality programming outputs from study initiation through regulatory approval and product launch. Requirements: MS or BS in a relevant scientific or technical discipline, with 10+ years (12+ for BS) of SAS programming experience in clinical trial environments, with strong knowledge of trial principles and regulatory standards. Proven leadership in managing cross-functional teams and multiple projects. Preferred: proficiency in additional languages like R or Python. High-value: experience in biotech/pharma, working on clinical trials for serious diseases, with an emphasis on global regulatory submissions. Work setup: hybrid onsite in Warren, NJ or Cambridge, MA, with some travel likely.