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臨床開発・薬事の求人322件応募資格・募集要項・仕事内容を見る
Medical Advisor (BONE)
- 給与
- 記載なし
- 勤務地
- 記載なし
- 休日
- 記載なし
- 雇用形態
- 記載なし
- ハイブリッド勤務
- 在宅勤務あり
どんな仕事かAIによる生成
The Medical Advisor (BONE) leads and develops the product medical strategy and plan, and works with the brand team on product strategy and lifecycle management. The role provides medical expertise, supports local and global studies, and leads evidence generation, publications, and medical events.
この求人に応募
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 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 10/18
- 職種
- 臨床開発・薬事
- 雇用形態
- 記載なし
- 給与
- 記載なし
- 勤務地
- Japan - 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
- 2026/07/24 13:03（87日前）
- 最終確認
- 2026/10/18 18:17（1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
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