Senior Manager Statistical Programming

BioSpace; New Jersey; On-site; USD 151,000 - 246,000; Full time

Job summary

Regeneron is seeking a Senior Manager, Statistical Programming to provide technical leadership across project teams, driving high-quality programming deliverables from single studies through regulatory approval and product launch.

Location options include Warren, NJ or Cambridge, MA with onsite work model. The role emphasizes mentorship, collaboration with global teams, and sponsorship of key regulatory submissions.

Qualifications

• Advanced SAS programming in a clinical data environment.
• Strong understanding of clinical trial principles and regulatory submission requirements.
• Proven ability to lead global, cross-functional teams.
• Experience managing multiple concurrent projects and mentoring junior programmers.
• Preferred knowledge of additional programming languages such as R or Python.

Responsibilities

• Lead programming support across multiple studies, ensuring timely, high-quality deliverables.
• Coordinate programming documentation and specifications, following established standards.
• Champion company values through excellence, collaboration, and accountability.
• Communicate proactively with study and project teams to clarify requirements and guide programmers.
• Lead submission-ready programming deliverables for global regulatory filings.
• Drive department goals and mentor/direct reports through goal-setting and coaching.

Skills

Advanced SAS programming

Cross-functional leadership

Mentoring

Project management

Communication

Education

MS or BS in Statistics/CS/Math/Engineering/Life Science

Tools

SAS

R or Python (preferred)

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 a Senior Manager, Statistical Programming to join our Statistical Programming function, providing technical leadership across project teams within one or more therapeutic areas. In this role, you will drive high-quality programming deliverables from single studies through regulatory approval, product launch, and beyond, while collaborating with partnering functions, external service providers, and study teams.

This position offers the opportunity to shape department strategy and mentor talent within a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & Where

Location: Warren, NJ or Cambridge, MA

Work model/flexibility: Onsite

Discover Your Role

• Lead programming support across multiple studies, ensuring timely, high-quality deliverables
• Coordinate programming documentation and specifications, following established standards
• Champion company values through excellence, collaboration, and accountability
• Communicate proactively with study and project teams to clarify requirements and guide programmers
• Lead submission-ready programming deliverables for global regulatory authority filings
• Drive department goals and serve as a subject matter expert on key topics
• Guide the development of direct reports through goal-setting, coaching, and mentoring
• Contribute to hiring by screening and interviewing programming candidates
• You bring advanced SAS skills honed in a clinical data environment, ideally across multiple therapeutic areas
• You understand pharmaceutical clinical development, statistical concepts, and regulatory submission requirements
• You collaborate naturally across global, interdisciplinary teams
• You juggle multiple projects and priorities without losing sight of quality
• You solve problems with initiative, creativity, and a self-starter mindset
• You enjoy influencing, mentoring, and coaching others toward strong results
• You lead with accountability and hold yourself to a high bar
• You're energized by both hands-on programming work and people leadership

This Role Requires

• MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline, with 10+ years (12+ for BS) of programming experience preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries, including some project and people management experience
• Advanced SAS programming expertise in a clinical data environment
• Strong understanding of clinical trial principles and regulatory submission requirements
• Proven ability to lead global, cross-functional teams
• Experience managing multiple concurrent projects and priorities
• Demonstrated mentoring or coaching experience with junior programmers
• Preferred/nice to haves: Knowledge of additional programming languages such as R or Python

#statprogregn

We are committed to building a workplace with an inclusive culture. 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.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$150,500.00 - $245,500.00