Manager, Statistical Programming - Internal Medicine

Regeneron Pharmaceuticals Inc.; Village of Tarrytown (NY); On-site; USD 129,000 - 210,000; Full time

Job summary

Regeneron Pharmaceuticals Inc. seeks a Manager of Statistical Programming to lead programming deliverables from a single study through regulatory approval, product launch, and annual reports. You will collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analyses and reporting.

Location options include Warren, NJ or Cambridge, MA with onsite work. A Master’s degree with 6+ years (or BS 7+) of relevant experience is required, and SAS experience is a

Qualifications

• Requires master's degree with 6+ years (or BS 7+) of relevant work experience.
• Experience leading programming deliverables within a clinical study team.
• Experience providing input on hiring, feedback, and performance evaluation.
• Strong organizational and documentation skills in a regulated environment.

Responsibilities

• Lead programming deliverables from a single study through regulatory approval, product launch, and annual reports.
• Develop and quality control tables, listings, and graphs to support analysis requirements.
• Manage programming effort and track progress and completion of deliverables, including complex ad hoc requests.
• Serve as programming representative on multidisciplinary study teams to ensure timely support through regulatory milestones.

Skills

Program management

Tables/Listings QC

Cross-functional collaboration

Hiring input

Communication

Analytical thinking

Adaptability

Documentation

SAS (certification)

Education

Master's degree

Bachelor's degree in related field

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 a Manager, Statistical Programming to join our Statistical programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting. This position offers the opportunity to contribute to 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:

• Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables
• Lead the development and quality control of tables, listings, and graphs in support of analysis requirements
• Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests
• Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch
• Partner with management to determine resource requirements for your therapeutic area or department
• Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles
• Provide feedback to management on team members' contributions to support performance evaluations and goal-setting
• Advise direct reports on procedures for data, records, and information retention
• Enjoy working with minimal supervision and taking ownership of complex deliverables
• Communicate clearly with cross-functional, multidisciplinary teams
• Think analytically and stay organized when managing multiple priorities and timelines
• Take initiative in developing deep expertise within a specialized area
• Bring a collaborative mindset to hiring, feedback, and team development
• Adapt easily to shifting priorities, including last-minute requests from senior leadership
• Approach quality and documentation with rigor in a regulated environment

This role requires:

• Master's degree with 6+ years (or BS 7+) of relevant work experience
• Proven experience leading programming deliverables within a clinical study team
• Experience providing input on hiring, feedback, and performance evaluation
• Strong organizational and documentation skills within a regulated environment
• Nice to have: SAS Certification

Does this sound like you?

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 on‑site. Please speak with your recruiter and hiring manager for more information about on‑site 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) $128,600.00 - $210,000.00