Vice President, US Medical Affairs

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Job description

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.

Summary

As a member of the Executive Leadership team for DS US Oncology Business Division, the Vice President, Medical Affairs will actively contribute to the creation, championing, and execution of the strategic direction and long-term vision for the Company. The position will also lead the Medical Affairs organization which is responsible for providing impactful medical support to the organization, outcomes research; publication planning; medical and product-related information; continuing education; Medical Affairs compliance, oversight to the field-based Medical Liaison group; and medical review of promotional materials, grants, and publications. This position will own and execute the scientific strategy to extend the life cycle of existing brands. The incumbent will have overall accountability and responsibility for generating and communicating accurate and meaningful medical and scientific information regarding all products. To accomplish these objectives the VP, Medical Affairs must also effectively collaborate with Clinical Research and other stakeholders to provide impactful scientific support for the Company's brands.

Responsibilities

- Serves as Lead medical advisor for the for the US Affiliate. Responsible for leading the medical and scientific support to all marketed products at Daiichi Sankyo. Lead the scientific effort that enables the company to achieve product market/sales objectives with scientific credibility.
- Lead the US Medical Affairs organization and ensure medical and scientific input to the strategies for all brands at Daiichi Sankyo. Ensure alignment with the business as well as RD. Oversight and accountability for the Medical Operating Plan and budgets.
- Lead and manage the teams responsible for Health Outcomes Research and any additional research activities necessary to support our products. Provide strategic input into the development and approval of Phase IIIb/IV trials in collaboration with global internal stakeholders. Overall accountability and responsibility for generating and communicating accurate and meaningful medical and scientific information regarding all products. Lead competitive intelligence activities of Medical Affairs, thereby creating awareness of competitor activities and scientific data generated in the relevant therapeutic areas. Ensure the timely initiation and completion of research projects as well as the accurate dissemination of data necessary to maximize the value of all products at Daiichi Sankyo.
- Lead and manage the teams responsible for accurate disclosure of data and clinical information regarding all products at Daiichi Sankyo as well as lead and manage the Field-based Medical Organization. Interact with key members of the medical community to assist in understanding current practice issues for strategically important therapeutic areas. Ensure alignment with other parts of the organization.
- Facilitate the effective positioning of the company to quickly uncover new business opportunities through product data, input from external healthcare professionals, medical support to licensing, and meaningful competitive intelligence activities.
- As requested, will review and sign off responsibilities for clinical trial SOPs and product labeling. Responsible for ensuring departmental compliance to all laws, rules, and regulations.

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)

- An advanced doctorate degree (PharmD, PhD, MD, DO or equivalent) in medical/ scientific area required
- MD preferred
- Experience in oncology therapeutic area required

Experience Qualifications
- 10 or More Years overall related experience required
- Post-graduate residency and/or fellowship training or equivalent experience required
- oncology or cardiovascular/metabolic disease experience preferred
- 10 or More Years clinical/research/academic experience, preferred
- 10 or More Years of pharmaceutical industry experience in Medical Affairs, strategically utilizing scientific data in various educational forums (e.g., grand rounds, symposia, consultant meetings, dinner programs, etc.). preferred
- Proven track record of working successfully with cross-functional teams to achieve business results. preferred
- successfully developing and implementing tactical business plans and project proposals in the assigned therapeutic areas. preferred
- experience managing departmental budgets. preferred
- experience managing scientific staff. preferred

Travel

Ability to travel up to 30% Ability to travel

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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