88-50100108 Statistical Programmer Analyst

Roche • Pleasanton, CA

5d • Remote

About The Position

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Roche Molecular Systems, Inc. seeks a Statistical Programmer Analyst at its Pleasanton, CA location. Duties: Within global healthcare technology company, serve as subject matter expert to lead, develop and review SAS (Statistical Analysis System) programs supporting clinical research teams with FDA compliance for regulatory submissions. Drive implementation and execution of programming deliverables across projects. Provide specialized technical programming expertise to others within own team or across Biometrics function. Design, develop, and validate compound-level SAS macros to standardize and automate clinical reporting deliverables (tables, listings, figures) across studies and business units. Transform and integrate multi-format data (CSV, Excel, SAS transport) into validated, analysis-ready datasets by transforming, merging diverse sources, and resolving complex data inconsistencies while ensuring end-to-end data integrity and traceability. Translate Statistical Analysis Plans into executable SAS/R code to generate regulatory submission packages for FDA filings. Create advanced statistical visualizations, diagnostic agreement reports, and interactive dashboards for clinical trial monitoring. Deliver modular, scalable, and reusable programming solutions that streamline reporting processes and support regulatory submissions with comprehensive validation documentation.

Requirements

• Bachelor’s degree, or foreign degree equivalent, in Computer Science, Engineering, Statistics or closely related field and 6 years of progressive, post-baccalaureate experience as a Statistical Programmer, SAS Programmer, Clinical Programmer, or closely related position in the medical diagnostics, medical device, or pharmaceutical industry.
• 6 years of experience with each of the following: Data Transformation and Integration through importing, cleaning, and merging multi-format data (CSV, Excel, Oracle) into SAS datasets
• Regulatory Reporting and Submissions including generating analysis datasets, tables, listings, and figures for FDA submissions
• Advanced Statistical Programming using SAS/R Programming Skills such as Modular, Scalable, and Reusable Code
• Translate statistical analysis plans into SAS code for accurate trial results
• Design, development, and validation of statistical software solutions and applying knowledge of statistical concepts
• Developing data insights and dashboards to monitor clinical trials data
• Can work 100% from anywhere in the U.S.

Responsibilities

• serve as subject matter expert to lead, develop and review SAS (Statistical Analysis System) programs supporting clinical research teams with FDA compliance for regulatory submissions
• Drive implementation and execution of programming deliverables across projects
• Provide specialized technical programming expertise to others within own team or across Biometrics function
• Design, develop, and validate compound-level SAS macros to standardize and automate clinical reporting deliverables (tables, listings, figures) across studies and business units
• Transform and integrate multi-format data (CSV, Excel, SAS transport) into validated, analysis-ready datasets by transforming, merging diverse sources, and resolving complex data inconsistencies while ensuring end-to-end data integrity and traceability
• Translate Statistical Analysis Plans into executable SAS/R code to generate regulatory submission packages for FDA filings
• Create advanced statistical visualizations, diagnostic agreement reports, and interactive dashboards for clinical trial monitoring
• Deliver modular, scalable, and reusable programming solutions that streamline reporting processes and support regulatory submissions with comprehensive validation documentation

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees