The Position
Senior Statistician
A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche.
This role is within Biostatistics, a core function within Product Development Data Science and Analytics (PDD) that provides strategic leadership and scientific rigor across Development at Roche. Biostatistics identifies opportunities to apply the full breadth of data, digital, and design capabilities to deploy innovative methods across PDD, PD and the broader Roche Pharma organization.
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to drive scientifically rigorous programmatic decisions across Roche's Development portfolio; Biostatistics designs robust trials and analysis plans that increase the probability of technical success, accelerating timelines to advance Roche's clinical pipeline and promote regulatory success - ultimately bringing medicines to our patients faster.
The Statistician is a key member of the cross-functional study or molecule team, responsible for applying statistical expertise to the design, conduct, analysis, and interpretation of individual clinical trials. This role ensures the scientific rigor and regulatory compliance of the study by contributing to protocol development, authoring statistical analysis plans, performing or overseeing data analyses, and supporting the interpretation and communication of results. The Statistician plays a critical role in ensuring that each study generates robust, meaningful data to support decision-making and regulatory submissions.
* You independently lead statistical input into clinical trial design, aligning with scientific objectives
* You own the development and quality review of statistical study documents
* You design and execute complex analyses, proactively resolving challenges
* You represent Biostatistics and PDD at the Study Team level, ensuring statistical and scientific rigor of study deliverables
* You collaborate proactively with cross-functional teams to align deliverables and timelines
* You interpret and communicate results in context, influencing study-level decisions
* You lead statistical contributions to CSRs and selected regulatory documents
* You provide functional guidance and informal mentoring to less experienced statisticians
* You may lead or influence study-level projects or contribute significantly to large project teams or initiatives
Who You Are:
* You hold an MSc or PhD in Statistics, Biostatistics, or a closely related quantitative field
* You have a minimum of 3 years of relevant experience in clinical trial statistics within a pharmaceutical, biotech, or CRO setting
* You have demonstrated experience contributing to the design, analysis, and interpretation of clinical studies across different phases
* You have a solid understanding of regulatory expectations and statistical methodologies for clinical developmentanalysis Wait, I truncated JSON. I didn't finish. I need to complete the JSON properly. That mid chunk ended prematurely. I also incorrectly inserted backticks in middle. Let me rewrite fully with correct content. We need to provide final JSON with the entire description. Must properly escape? All content inside JSON string. The content contains apostrophes (e.g., It's, Roche's). Those are fine inside JSON string. Need to ensure no double quotes inside; we have none. Need to close JSON properly. Let's rewrite fully. Ensure closing braces. Also ensure no extra characters. Let's craft description string. We'll use the fully cleaned content. Let me copy earlier content but fix minor errors. Check earlier content for garbled bit: The phrase "... ensuring scientific rigor across Roche's Development portfolio;..." remain. The extra 'n in
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