Manager, Statistical Programming - Internal Medicine

Regeneron Pharmaceuticals
Location
Warren
Job Type
Full-time
Posted
October 11, 2026
Salary Range
$129k - $210k USD

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

#statprogregn

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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.

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

#statprogregn

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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 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

Frequently Asked Questions

Where is this job located, and what is the work mode?
The position is based on-site in Warren, NJ or Cambridge, MA.
What qualifications and experience are required for this role?
Candidates need a Master's degree with 6+ years of relevant experience, or a Bachelor's degree with 7+ years. Proven experience leading programming deliverables on a clinical study team, providing input on hiring and performance evaluations, and strong organizational skills in a regulated environment are required. A SAS Certification is nice to have.
What are the key responsibilities of this position?
You will lead programming deliverables, oversee the development and quality control of clinical tables, listings, and graphs, manage resource requirements, represent programming on multidisciplinary study teams, and assist with hiring and screening candidates. You will also provide feedback on team member performance and advise direct reports on data retention procedures.
What is the salary range for this role?
The annual salary range for this position is $128,600.00 to $210,000.00.
What benefits does Regeneron offer?
Regeneron's total rewards package may include annual bonuses, equity awards, pension or retirement benefits, a 401(k) company match, health and wellness programs, medical, dental, vision, life, and disability insurance, paid time off, family support benefits, and access to fitness centers.

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Job Information

Source: manual
AI Relevance: 80/100 (Highly relevant)
Remote Type: onsite
Allowed Locations: Worldwide
Skills & Tags:
regeneron pharmaceuticals clinical

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