Lead Statistical Programmer - Genetic Medicines

Regeneron Pharmaceuticals, Inc (USA); Kentucky; On-site; USD 110,000 - 179,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio onsite in Warren, NJ or Cambridge, MA.

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

Qualifications

• 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.

Responsibilities

• 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.

Skills

Programming experience

Analytical thinking

Documentation

Team collaboration

Education

Master's degree

Tools

SAS

Job description

Regeneron Pharmaceuticals, Inc. seeks a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio onsite in Warren, NJ or Cambridge, MA.

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