Senior Statistical Programmer - Clinical Trials Lead

Regeneron Pharmaceuticals; Cambridge; On-site; GBP 82,000 - 133,000; Full time

Job summary

Regeneron Pharmaceuticals is seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. You will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring documentation is high quality and compliant.

This role involves leading programming activities, coordinating timelines with study teams, and contributing to submissions and 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.

Skills

Clinical data programming

Documentation quality

Regulatory collaboration

Education

Master’s degree

Job description

Regeneron Pharmaceuticals is seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. You will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring documentation is high quality and compliant.

This role involves leading programming activities, coordinating timelines with study teams, and contributing to submissions and regulatory