Principal Statistical Programmer
regeneron · Warren ·
- Seniority
- Principal
- Experience
- 3+ years
- Salary
- USD 109,900 – 179,300 / year
Lead statistical programming for clinical trials, producing analysis datasets, tables, listings, and graphs while ensuring regulatory compliance and collaborating with cross-functional teams.
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
This role might be for you if you:
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
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 . 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)
$109,900.00 - $179,300.00