Tokyo Pfizer Full time

Specialty Care Medical Affairs Lead, Japan

Pfizer seeks top talent to innovate and bring therapies to patients. As a Specialty Care Medical Affairs Lead in Japan, you will lead a dedicated medical affairs team, develop the Medical Plan and Strategy for specialty care, and collaborate with internal and external stakeholders.

  • Provide leadership to a dedicated medical affairs team.
  • Be responsible for development of the Medical Plan and Strategy for specialty care.
  • Be a member of the Country Medical and the Specialty Care Commercial Leadership Team.
  • Ensure compliance of medical team with country Code of Practice and relevant procedures, regulations and guidelines.
  • Work closely with internal and key external stakeholders supporting Pfizer strategy and bringing medical insights as well as support for media, government and patient group activities, including policy development, corporate initiatives and issues management.

Responsibilities:

  • Leadership of medical team, including setting business objectives, performance management and team development.
  • Responsibility for development of the Medical Plan/Strategy for relevant therapeutic areas.
  • Recruitment, development and retention of talented colleagues.
  • Membership of Medical and Commercial Leadership Teams.
  • Resource allocation to ensure appropriate resources to fulfill medical objectives and business needs.
  • Ensure compliance of medical team with country Code of Practice and relevant SOPs, regulations and guidelines.

Requirements:

  • Medical Doctor degree, with knowledge in Cardiology, Endocrinology, Immunology (Gastroenterology, dermatology, rheumatology), Hematology and/or Gene therapy.
  • Significant pharmaceutical industry experience and excellent understanding of the local healthcare environment.
  • Qualifications to act as in-country signature, or have qualifications and potential to become a medical signatory is mandatory.
  • Excellent communication and presentation skills.
  • Good knowledge of pharmaco-vigilance and regulatory legislation and how it impacts the product portfolio.

The estimated salary for this position is approximately ¥20,000,000 - ¥30,000,000 per year, depending on experience.



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