Senior Statistician

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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 statistics 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 Senior
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 and own the development and quality review of statistical study documents

• You design and execute complex analyses, proactively resolving challenges and 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 and 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 and may lead or influence study-level projects or contribute significantly to large project teams or initiatives

• You hold an MSc or PhD in Statistics, Biostatistics, or a closely related quantitative field and 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 and have a solid understanding of regulatory expectations and statistical methodologies for clinical development

• You are proficient in SAS and/or R and familiar with CDISC standards

• You are able to work autonomously while collaborating effectively in cross-functional teams and demonstrate capacity for independent thinking and ability to make decisions based upon sound principles

• You bring excellent strategic agility including problem-solving and critical thinking skills, and agility that extends beyond the technical domain and demonstrate respect for cultural differences when interacting with colleagues in the global workplace

• You have excellent verbal and written communication skills, specifically in the areas of presentation and writing, with the ability to explain complex technical concepts in clear language

Preferred:

• Experience working in cross-functional global study teams and effective communication skills with the ability to…