Job Title: Associate Director, Medical Affairs Strategy
We are seeking an experienced and skilled Associate Director to join our Medical Affairs team in Japan. This role will be responsible for developing and executing the medical strategy and tactics for designated Cell Therapy products in Japan.
The ideal candidate will have a strong background in medical affairs, with experience in planning and executing medical strategies, as well as a proven track record of collaboration with cross-functional teams.
Key Responsibilities:
- Develops the Medical Affairs strategy and tactics for designated Cell Therapy product(s) in Japan, including data generation and 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, support for clinical trials and real world evidence (when requested), publication plans, and investigator-sponsored studies
- Works with the cross-functional brand and launch team
- Develops and conducts medical education and communication activities, including digital, face-to-face, and print
- Provides scientific and medical input to scientific publication activities
- Works collaboratively with KITE & Gilead personnel in Sales, Marketing, Market Access, Clinical Research, Global Safety, Public Affairs and Governmental Affairs
- Works collaboratively with the Gilead Japan Medical Affairs team
- Responds to clinical inquiries regarding marketed or developmental KITE products
- Presents scientific and clinical data for these products. Utilizes scientific resources to deliver impactful presentations in a variety of different settings
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
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
Estimated Salary: $150,000 - $200,000 per year
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