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Sr Manager, Medical Strategy

Japan - TokyoMedical AffairsRegular

Arbeitsbeschreibung

Key Responsibilities

  • Leads and develops the Medical Affairs strategy and its tactics for designated Cell Therapy product(s) in Japan, including data generation and data dissemination plan.
  • Executes Medical Affairs activities and scientific projects based on the medical strategy and Plan of Action, including tactical deliverables such as advisory board, and real-world evidence (when requested), publication plans, and investigator-sponsored studies, in close collaboration with other medical team members.
  • Works with Global Medical Affairs counterparts and serves as representative from Japan in relevant global meetings.
  • Works collaboratively with the other Medical Affairs TA team
  • Co-leads and works with the cross-functional brand and launch team.
  • Develops and conducts medical education and communication activities, including digital, face-to-face, and print.
  • Provide scientific and medical input to scientific publication activities.
  • Works collaboratively with Kite & Gilead personnel in Marketing, Market Access, Research, Clinical Development, Patient Safety, Public Affairs and Governmental Affairs.
  • Responds to clinical inquiries regarding marketed or investigational Kite products.
  • Presents scientific and clinical data for these products. Utilizes scientific resources to deliver impactful presentations in a variety of different settings.
  • Assists with Kite post-marketing surveillance program that includes collaboration with investigators and internal Gilead personnel. Assists with site selection for both Phase IV and other clinical trials.

Basic Qualifications and Requirements

  • Advanced degree (i.e. MD, PharmD, PhD) preferred or may have a BS/MS in pharmacy with varying levels of clinical and/or industry experience.
  • Solid pharmaceutical company experience with a good exposure in Medical Affairs
  • Proven track record of planning and executing a medical affairs plan
  • Experience in the management or investigation of clinical trials is highly desirable.
  • Must be fully cognizant of all relevant scientific data and regulatory requirements for field-based
  • Industry and Medical Affairs experience required, preferably in hematology /oncology or Cell Therapy

Preferred Qualifications and Requirements

  • Ability to adapt in a constantly evolving environment
  • Self-motivated with a strong sense of ownership in areas of responsibility
  • Excellent written and verbal communication skills in Japanese and English
  • Must be committed to continuing education to maintain knowledge base
  • Must have the ability to work as a member of several teams that may overlap such as national MS team, regional sales team, national accounts, and others.
  • Utilizes scientific resources for impactful presentations in a variety of different setting
  • Enjoy working in a fast-paced entrepreneurial environment
  • Strong desire for cross functional teamwork