**Join a Legacy of Innovation 110 Years and Counting!** Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. Under the Group’s 2025 Vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. **Summary** This position provides support of secondary data studies in the study design, statistical analysis, interpretation of results with some supervision. This position interacts with study teams to provide statistical and scientific expertise in the project deliverables. This position is also expected to provide an excellent communication with people from the different functions. This position works under some supervision to solve study/analytics problems. **Responsibilities** - Secondary Data Study Protocol Development, Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and study report: Supports statistical activities for studies including study design, protocol development, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and study report input and review. Acts as main statistical contact for the assigned studies and projects. Work effectively with the study team to support and provide the planned deliverables. - Real-World Evidence (RWE) Activities: Provides guidance in scientific and statistical aspects of RWE activities and support deliverables to ensure the quality. RWE activities include the real-world data (RWD) inquires, RWD/E consultation, and the feasibility assessment using the secondary data. Work closely with the business partner to support and provide the planned deliverables. - Excellent Communication: Work effectively with the customers/stakeholders and clearly communicate the statistical and scientific input in the design, conduct, analysis, and results interpretation. - RWE Analytics: Foster new methodology and provide innovative analytics technique method (e.g. External Control Arm, machine learning, predictive model). **Qualifications:** Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation. **Education Qualifications (from an accredited college or university)** - PhD in Statistics or Biostatistics or pharmaco-epidemiology or other related field preferred - Master's Degree in Statistics/Biostatistics or pharmaco-epidemiology or other related field preferred **Experience Qualifications** - 4 or More Years relevant experience in the pharmaceutical industry with Ph.D preferred - 4 or More Years with Masters preferred Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. At the heart of Daiichi Sankyo, Inc. is the fundamental belief that each employee helps shape our success. We have created an exceptional working environment that values and rewards individual contributions, but we also believe in the power of collaboration. We provide employees with the training, tools and technology that they need to excel. Our open communication, emphasis on results, and spirit of personal accountability are hallmarks of our corporate culture and ensures that each employee’s unique abilities are valued and utilized. We invite you to consider a career at Daiichi Sankyo, Inc.