Principal Statistical Programmer

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
- 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
- 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

Application Instructions
- Apply now.