Principal Statistical Programmer - Genetic Medicines

Regeneron Pharmaceuticals, Inc; New Jersey; On-site; USD 110,000 - 179,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study portfolio across the clinical program.

You will provide programming leadership, develop and test program logic, and ensure documentation quality to support regulatory submissions and beyond. The role requires a Master’s degree with 3+ years of relevant experience, onsite in Warren, NJ or Cambridge, MA, and collaboration within multidisciplinary teams to

Qualifications

• Master's degree with 3+ years of relevant experience.
• Experience in programming for clinical study data and analysis deliverables.
• Strong documentation and quality control in a regulated environment.
• Experience collaborating within a multidisciplinary study team.

Responsibilities

• Support or lead programming and QC of analysis datasets, tables, listings, and graphs.
• Coordinate activities and communicate shifting timelines and milestones to the study team.
• Create and maintain programming specifications for analysis datasets across studies.
• Support creation and validation of submission requirements, including annotated CRFs and define documents.
• Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch.
• Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed.
• Participate in department working groups, contributing to tool development and process improvement.
• Design and test program logic independently, maintaining documentation in a regulated environment.
• Enjoy working independently while staying closely connected to a broader study team.
• Communicate clearly and proactively, especially around shifting timelines.
• Take pride in accuracy and consistency when documenting and maintaining code.
• Think analytically and enjoy solving programming and data challenges.
• Stay curious about process improvement and enjoy contributing ideas to working groups.
• Adapt comfortably to ad hoc requests and evolving priorities from senior leadership.
• Bring attention to detail and a quality mindset to regulated work.

Skills

Statistical programming

Data analysis

Documentation

Regulatory knowledge

Cross-functional collaboration

Education

Master's degree

Tools

SAS

R

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 Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory approval and beyond.

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:

• Support or lead programming and quality control of analysis datasets, tables, listings, and graphs
• Coordinate activities and communicate shifting timelines and milestones to the study team
• Create and maintain programming specifications for analysis datasets across studies
• Support creation and validation of submission requirements, including annotated CRFs and define documents
• Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch
• Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed
• Participate in department working groups, contributing to tool development and process improvement
• Design and test program logic independently, maintaining documentation in a regulated environment
• Enjoy working independently while staying closely connected to a broader study team
• Communicate clearly and proactively, especially around shifting timelines
• Take pride in accuracy and consistency when documenting and maintaining code
• Think analytically and enjoy solving programming and data challenges
• Stay curious about process improvement and enjoy contributing ideas to working groups
• Adapt comfortably to ad hoc requests and evolving priorities from senior leadership
• Bring attention to detail and a quality mindset to regulated work

This role requires:

• Master's degree with 3+ years of relevant experience
• Proven programming experience supporting clinical study data and analysis deliverables
• Strong documentation and quality control skills within a regulated environment
• Experience collaborating within a multidisciplinary study team

#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.

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.

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)

$109,900.00 - $179,300.00