Overview Join a Legacy of Innovation 125 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 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 18,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, 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 Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director, USMA Oncology (US Medical Affairs team lead for compound), is responsible for assisting with defining compound/program medical strategies and for leading select medical affairs projects within a specific compound or indication. The role is primarily responsible for US Medical Affairs Strategy and overseeing execution of medical activities for assigned indication(s) and asset(s) and will have the responsibility of managing multiple direct reports. Responsibilities Lead the development of the US Medical Affairs strategy and execution of the US Medical Affairs plan for select indications/projects related to evidence generation, medical information and internal education, publications, scientific exchange and external data communication, and stakeholder scientific engagement. Manage budgets and resources for the assigned medical affairs plan activities, in collaboration with Sr. Director. Lead medical readiness activities for market launches, including strategic partnerships with the brand team, HEOR, RD, FMA, MIE and global functions to create and implement strategies that support launch. Provide medical support/input into commercial and market access discussions for select indications. Provide medical leadership in interactions with key external stakeholders including scientific leaders, payers and societies; lead Scientific Engagement activities such as planning advisory boards, managing stakeholder interactions and peer-to-peer discussions, congress engagement activities, and collation of insights for select indications related to the compound. Responsible for scientific communications and publications; interpretation of clinical data; ensuring consistency of clinical content and scientific statements across materials; training or communication of emerging data (internal or competitive); budget and forecast accuracy. In a matrix environment, represent US interests and business needs in shaping development and life cycle management strategy for select indications/projects. Review ESRs and may serve as deputy regional medical lead in Global IIS Review Committee meetings. May serve as medical lead for select company-sponsored evidence generating studies/projects. Manage all medical aspects such as study document development and drive execution for assigned projects in collaboration with USMA Clinical Operations and other cross-functional and regional stakeholders. Qualifications Education Qualifications (from an accredited college or university) An advanced doctorate degree (PharmD, Ph.D., MD, DO, or equivalent) in a medical/scientific area is required. Experience in oncology therapeutic area is required. Experience Qualifications 10 or more years of overall related experience or commensurate education/experience required. 4 or more years of experience in pharma at local, regional and/or Global level preferred. Excellent knowledge of current clinical practice in Oncology/Hematology or other relevant disease area preferred. Knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products preferred. Travel Ability to travel up to 20%. Standard office based physical demands, travel as 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. Salary Range: $198,160.00 - $297,240.00 [Link available when viewing the job]

#J-18808-Ljbffr