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Roche Holding AG recherche un Senior Statistician pour intégrer l'équipe Biostatistics à Basel, afin d'appliquer l'expertise statistique tout au long du design, de la conduite et de l'interprétation des essais cliniques.
Le rôle assure rigueur scientifique et conformité réglementaire, avec des contributions aux CSR et documents réglementaires, et un mentorat pour statisticiens moins expérimentés.
Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte.
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 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 translate complex statistical concepts for non-statistical audiences.
Experience with multiple phases of drug development (early and/or late stage) and experience in mentoring or scientific leadership within a matrix organization.
Strategic mindset with the ability to contribute to portfolio-level decisions
This position is based in Basel and relocation assistance is not available
Un avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial.
Construisons ensemble un avenir plus sain.
Roche est un employeur offrant l'équité en matière d'emploi.