Vice President, Global Team Lead Oncology
1 week ago
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 120 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. 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.
Job Summary:
The Vice President, Global Team Lead is a senior, cross-functional leader in Daiichi Sankyo's global R&D organization. The role reports to the Head of Asset and Portfolio Management. The VP – Global Team Lead is a member of the Asset and Portfolio Management Leadership Team whose vision is to transform next-generation science into medicines valuable to patients and contribute to the transformation of Daiichi Sankyo. The VP GTL is directly responsible for conceiving, designing and implementing product strategy and development delivery for their assigned program through the life cycle. Depending on specific program and its stage of life cycle, the VPGTL has senior accountabilities that are critical to the delivery of R&D goals and portfolio targets.
Responsibilities:
Creating and leading 1-2 high performing project cross-functional teams of accountable global senior leaders which is responsible for the identification and articulation of a competitive efficient and effective development strategy and execution. That strategy will provide for a differentiated clear and sustainable platform of evidence generation, design and leadership of asset development and addressing all regulatory, drug and patient safety, data, CMC, IP, Market Access and all other relevant functions on the Global Project Team
Contributing to the delivery of the comprehensive Research and Development portfolio to maximum value, including the identification and delivery of cross-portfolio opportunities, the development and growth of scientific leadership, cross-functional development acumen, project management capability and robust peer review of projects and products
Leading personal and corporate relationships with external Key External Experts (KEEs)s and research scientists, collaborators, and other external stakeholders; Collaborating with external partners to deliver existing commitments and to explore additional opportunities
Managing asset budget to ensure planning and spending is within approved budgets and consistent with established operating expense goals and in line with DSI’s processes, Functioning as an expert liaison between the intra and intercompany leaders
Ensuring development and effective implementation of high-quality asset strategies across the life cycle. Providing direction to the Global Project Team in support of asset strategy to include but not limited to regulatory submissions and interactions including preparation of documents for regulatory filings including responsibility for overseeing these strategies. Lead individuals in the cross functional team with the aim of contributing to optimal individual development and accomplishment.
Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.
Education:
MD with substantial industry-based experience as team leader preferred or
PhD with substantial industry-based experience as team leader preferred or
Master's Degree with substantial industry-based experience as team leader preferred
Experience:
10 or More Years Successful drug development record with proven credibility and a to include regulatory submissions in more than one major market.
Minimum years of relevant industry experience of 10 years drug development with experience leading cross-functional teams across the life cycle of an asset. In specific therapeutic areas, specific experience in these areas of at least 7 years will be required required
Travel:
Ability to travel up to 50% Conferences, program specific meetings and intracompany meetings
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.
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