Paris Senior Manager, Biostatistics (Late Stage) (mfd) 92500

Job description

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary Position leads complex studies in study design, statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. This position also guides contract research organization (CRO) programmers and statisticians in preparing analysis files and performing statistical analyses. Additionally, this position interacts with study teams, as well as statisticians and programmers at CROs. This position works under some supervision to solve complex study problems. The primary location for this position is France, with Germany as the secondary location. Responsibilities Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR). Leads statistical activities for complex studies, including study design, protocol development, CRF review, SAP development, analysis file development, statistical analysis accuracy validation, results interpretation, and CSR input and review. Acts as the main statistical contact for the assigned studies and projects. Provides guidance to the study team on all aspects of statistical activities; collaborates closely with the data manager to ensure high-quality data. Drug Development Strategy: Provides input to multiple aspects of the development plan to ensure the study designs at each phase of development are scientifically sound, can fulfill regulatory requirements, and deliver the pre-specified product profile. CRO / Vendor Oversight: Reviews CRO/vendor proposals and budgets. Establishes procedures through regular interaction, setting expectations for deliverables and timelines to guide CRO biostatisticians and statistical programmers on complex studies. Ensures deliverables are accurate and delivered according to the timelines. Global Health Authority Interaction / Negotiation: Contributes to documents submitted to Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meetings or teleconferences with Health Authorities. Global BDO Strategy to Improve Drug Development: Primarily participates in and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development, which leads to cost savings and shortened timelines for the company. Qualifications Education Qualifications Master’s degree in statistics or biostatistics required. PhD in statistics or biostatistics preferred. Experience Qualifications 8+ years of relevant experience in the pharmaceutical industry with a master’s degree required. 5+ years of relevant experience in the pharmaceutical industry with a PhD preferred. Travel Requirements Ability to travel up to 10% of the time. Why work with us? Working at Daiichi Sankyo is more than just a job – it is your chance to make a difference and change patients’ lives for the better. We can only achieve this ambitious goal together. That is why we foster a culture of mutual respect and continuous learning, with a strong commitment to inclusion and diversity. Here, you will have the opportunity to grow, think boldly, and contribute your ideas. If you have a proactive mindset and passion for addressing the needs of patients, we eagerly await your application. Apply now Privacy Policy Visit DaiichiSankyo.com © 2026 Daiichi Sankyo, Inc. All Rights Reserved. Cookie Consent Manager When you visit any website, it may store or retrieve information on your browser, mostly in the form of cookies. Because we respect your right to privacy, you can choose not to allow some types of cookies. However, blocking some types of cookies may impact your experience of the site and the services we are able to offer. Required Cookies These cookies are required to use this website and can't be turned off. 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