88-50100108 Statistical Programmer Analyst

Roche • Pleasanton, CA

6d • 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. Education and experience required: 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. Special Requirements: 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. #LI-DNI #DNI #DE-DNI Worksite: 4300 Hacienda Drive, Bldg 727, Pleasanton, CA 94588 The expected annual salary range for this position based on the primary location for this position of Pleasanton, CA is $140,136 to $181,200 per year. Actual pay within the range will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits (https://roche.ehr.com/default.ashx?CLASSNAME=splash) Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. We are Roche.

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 Data Transformation and Integration through importing, cleaning, and merging multi-format data (CSV, Excel, Oracle) into SAS datasets
• 6 years of experience with Regulatory Reporting and Submissions including generating analysis datasets, tables, listings, and figures for FDA submissions
• 6 years of experience with Advanced Statistical Programming using SAS/R Programming Skills such as Modular, Scalable, and Reusable Code
• 6 years of experience to Translate statistical analysis plans into SAS code for accurate trial results
• 6 years of experience with Design, development, and validation of statistical software solutions and applying knowledge of statistical concepts
• 6 years of experience with Developing data insights and dashboards to monitor clinical trials data

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