Associate Director Statistical Programming

Regeneron Pharmaceuticals, Inc (USA); Kentucky; Hybrid; USD 180,000 - 240,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Regeneron Pharmaceuticals, Inc. seeks an Associate Director, Statistical Programming to join our Statistical Programming team in a hybrid work model.

You will oversee programming activities across internal and external partners, shaping standards, processes, and training while delivering high-quality analyses for therapeutic programs. You will collaborate with study teams, leadership, and cross-functional stakeholders to meet analytical and computing needs, set goals, mentor staff, and

Qualifications

• Master's degree and 10+ years of clinical programming experience.
• Proven project and people management across global teams.
• Experience with regulatory submissions in pharmaceutical development.

Responsibilities

• Lead and manage a statistical programming group and external providers.
• Shape standards, applications, processes, and training for the therapeutic area.
• Collaborate with study and project teams to align requirements and guide execution.
• Represent Programming with partnering functions to meet computing needs.
• Mentor staff and contribute to hiring.

Skills

Advanced SAS programming

Project management

People leadership

Cross-functional collaboration

Education

Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline

Tools

SAS

Job description

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Statistical Programming to join our Statistical Programming team, supporting our therapeutic area programs in a hybrid work model. In this role, you will oversee statistical programming activities across internal teams and functional service providers, ensuring high-quality deliverables while shaping departmental standards, processes, and training. You'll collaborate closely with study and project teams, programming leadership, and cross-functional stakeholders to meet therapeutic analysis and computing needs.

Location: Warren, NJ
Work model/flexibility: Onsite/hybrid

Responsibilities

• Lead and manage a statistical programming group, driving timely, high-quality deliverables across internal and outsourced work
• Shape and implement programming standards, applications, processes, and training for your therapeutic area
• Partner with study and project teams to clarify requirements and guide programmers through assignment execution
• Represent Statistical Programming with partnering functions to ensure specifications and computing needs are met
• Champion company values, modeling excellence, collaboration, ownership, and accountability
• Drive department goals and lead subject‑matter‑expert initiatives
• Set goals, manage performance, and mentor direct reports, supporting their growth and development
• Contribute to hiring by screening and interviewing programming candidates

Preferred Attributes

• Bring proven experience managing programming teams and external service providers
• Think strategically about department‑wide standards, processes, and long‑term goals
• Communicate confidently across global, cross‑functional teams
• Solve problems independently and manage multiple priorities under tight timelines
• Enjoy mentoring and developing junior staff and contractors
• Take ownership of deliverables without close supervision
• Bring a collaborative, respectful, and solutions‑oriented mindset to complex projects

Qualifications and Requirements

• Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline, with 10+ years of clinical programming experience
• Advanced SAS programming skills (Base, Stat, Macro, Graph) within a clinical data environment
• Demonstrated project and people management experience, including work across global, interdisciplinary teams
• Expertise in one or more therapeutic areas and strong understanding of pharmaceutical clinical development and regulatory submissions

Nice to haves

• SAS certification
• Leadership experience supporting the hiring, development, and evaluation of junior staff and contractors

Equal Opportunity Statement

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), 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. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.