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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

The purpose of this position is to analyze single Population PK/PD Phase 1 to 3 studies, simulate multiple dose scenarios, and write M&S study report for Phase 1 to 3 studies. This position demonstrates general knowledge of Phase 1 studies and multiple dose scenarios, PK/PD M&S analysis data structures and analysis tools requirements, simple disease models, regulatory guidelines pertaining to M&S, and programming and analytical software. This position works independently in simpler studies/models and interacts with internal project teams.

Responsibilities

• Analyzes and presents MS Analyses of Phase 1 - 3 studies

• Simulates multiple dose scenarios; characterizes the time course of disease progression using relatively simple disease models

• Writes MS study reports for Phase 1 to 3 studies

• Interacts effectively on internal project teams as well as independently in simpler studies/models

• Works with and influences the interactions between candidate drug and its immediate target

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 pharmacology or pharmaceutical sciences or PharmD with a clinical pharmacology research fellowship required

Experience Qualifications

• 1+ years Industry Experience required

• 1+ years' experience with the following systems: NONMEM, R, PsN, XPose, WinNONLIN (Phoenix), WinBUGS, MONOLIX required

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.