Exciting opportunity to drive scientific rigor and regulatory compliance in clinical trials within Roche’s Biostatistics team. Lead statistical analysis, contribute to protocol development, and collaborate with cross-functional teams. Ideal for candidates with significant experience in clinical trial statistics and strong analytical skills.
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.
Tasks
- Independently lead statistical input into clinical trial design, aligning with scientific objectives and own the development and quality review of statistical study documents.
- 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.
- Collaborate proactively with cross-functional teams to align deliverables and timelines and interpret and communicate results in context, influencing study-level decisions.
- Lead statistical contributions to CSRs and selected regulatory documents.
- 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.
Requirements
- MSc or PhD in Statistics, Biostatistics, or a closely related quantitative field and a minimum of 3 years of relevant experience in clinical trial statistics within a pharmaceutical, biotech, or CRO setting.
- Demonstrated experience contributing to the design, analysis, and interpretation of clinical studies across different phases and a solid understanding of regulatory expectations and statistical methodologies for clinical development.
- Proficient in SAS and/or R and familiar with CDISC standards.
- 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.
- Excellent strategic agility including problem-solving and critical thinking skills, and agility that extends beyond the technical domain.
- Demonstrate respect for cultural differences when interacting with colleagues in the global workplace.
- 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 translate complex statistical concepts for non-statistical audiences.
- Preferred: Experience with multiple phases of drug development (early and/or late stage) and experience in mentoring or scientific leadership within a matrix organization.
- Preferred: Strategic mindset with the ability to contribute to portfolio-level decisions.
Bist du Teil dieses Unternehmens?
Dieses Unternehmensprofil wurde automatisch erstellt. Wenn du für Roche Schweiz arbeitest, kannst du das Profil jetzt beanspruchen und verifizieren – kostenlos und in wenigen Minuten.
Über uns
Das Team
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 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.