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The (Senior) Medical Advisor (I&I) leads and develops product medical strategy and plans, and works with the brand team and local commercial team on product strategy. The role leads local medical activities and supports study planning and execution, medical programs, advisory meetings, and expertise for pipeline products and reimbursement requests.
応募資格
必須
- Master’s degree in life-science or relevant area, equivalent education history
- Minimum of 2 years in pharmaceutical industry, or proven industry collaboration in academia
- Experience in developing and executing Medical strategy for pre-launch products.
- Experience in Medical Department or Clinical Development
- Experience with clinical study management and conduct
- Knowledge of commercialization and business practices
- Fluent in Japanese and English
歓迎
- MD, PharmD or PhD is strongly preferred
- Knowledge of pharmaceutical product development, product lifecycle and commercialization process with advanced understanding of other functions; including, but not limited to, Clinical Operations, Commercial, Regulatory, and Medical Affairs
- Therapeutic area knowledge and experience is preferable
- Network of customer contacts in therapeutic area
- Finance and budgeting experience
- Capability of office works and project managements
募集要項最終確認 9/25
- 職種
- MR
- 雇用形態
- 記載なし
- 給与
- 記載なし
- 勤務地
- 東京都Tokyo
- 働き方
- WORK LOCATION TYPE: Flex Commuter / Hybrid
- 経験年数
- 2年以上
- 学歴
- 大学院修了以上
- 掲載日
- 2026/07/31 02:11（60日前）
- 最終確認
- 2026/09/25 18:28（4日前）
仕事内容
Job purpose
Lead and develop product medical strategy and plan based on product strategy.
Key member in the brand team to develop product strategy with and local commercial team.
Provide Japan position on global/region disease and product related programs.
Provide medical affair consideration on portfolio evaluation and discussion.
Lead the planning and execution of evidence generations, publications and medical events.
Key responsibility
Partners with the brand team in the development and execution of the Local product(s) lifecycle management plan
Leading and developing the Local Medical strategy and Medical activities for the product(s) in accordance to internal and external regulations
TA and/or product specific Medical training
Ensuring consistency of Medical content and scientific messages across various tools and materials
Visits selected KOL’s and study groups for strategic discussions and protocol development
Develops study protocols for Local Amgen sponsored studies (AST); supports and executes Local study protocol preparation, filing, review and approval in line with
Amgen processes and policies
Works with Global Study Operations (GSO) to ensure preparation, implementation and completion of ASTs
Supports GSO in participation and completion of global/region studies in the country, including provision of input into site selection
Reviews Local ISS proposals prior to approval and ensures appropriate
Local/region/global committee review, if applicable
Oversees in-sourced/out-sourced medical programs and logistics
Participates in/conducts Local Advisory Board Meetings, Investigator Meetings and/or Expert Panels
Provides Medical expertise for pipeline products
Provides Medical expertise for Health Economy and reimbursement requests
Competencies
Medical/scientific expertise, and business acumen
Fluency in English, both oral and written communications
Strong communication and presentation skills
Continuously expanding medical and scientific knowledge as well as
market knowledge
Strong clinical research knowledge (study design, study evaluation, medical writing skills, expert panel conduct, symposium and workshop management, KOL management)
Strong customer orientation; science-based
Ability to work in a cross-functional team (e.g., Commercial, Clin Development, EU teams, HE, Regulatory, Safety, etc.)
Role model for others in line with Amgen Values
Demonstrates leadership skills
この求人はアムジェン株式会社の採用ページの掲載内容をもとに構成しています。応募条件の最新情報は募集元をご確認ください。
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