Lead Statistical Programmer – Genetic Medicines (Onsite)

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

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