Manager Statistical Programming

Note: This is an onsite opportunity and not eligible for remote work. Manager Statistical Programming Provides timely support to the study team on all programming matters according to project strategies. As an integral part of a study team, the incumbent leads programming for processing data from clinical studies, ensuring compliance with Statistical Analysis Plans, programming specifications, and internal standards and guidelines. Responsible for delivering programming deliverables from the single study through regulatory approval, product launch, data monitoring boards, and annual reports. Oversees documentation, code, logs, and output within a regulated environment and meets statistical ad‑hoc requests from senior management. Typical Responsibilities Develop expertise within a therapeutic area or standard tool; work with minimal supervision to prepare, execute, report, and document projects. Act as lead programmer in development and QC of tables, listings, graphs, or systems using Regeneron tools and CDISC SDTM/ADaM. Manage programming effort, including e‑submission deliverables, using appropriate tools to track and summarize work required, progress and completion. Provide programming support for complex presentations and statistical ad‑hoc requests. Represent programming in multidisciplinary study teams to ensure timely and quality support for analysis and reporting up to regulatory approval and product launch. Lead application development and serve as the programming representative to the user audience when applicable. Work with management to determine resource requirements for therapeutic area or departmental functions. Review, screen, and interview candidates for contractor and permanent positions; provide feedback on team contributions and performance evaluations. Advises direct reports on data retention and record-keeping procedures. Qualifications Master’s Degree. 8–10 years of relevant work experience. Desirable SAS certification. Alternatively, 5+ years of programming experience in processing clinical trial data in biotechnology, pharmaceutical, or health‑related industry, with project and people‑management experience and a Master’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline. Salary Range (annually) $128,600.00 – $210,000.00 Equal Employment Opportunity Regeneron is an equal‑opportunity employer and commits to building an inclusive culture. All qualified applicants will receive consideration for employment without regard to race, color, religion or belief, sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Reasonable accommodation will be provided to applicants with disabilities or chronic illnesses during the recruitment process unless such accommodation would impose undue hardship. #J-18808-Ljbffr