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| 採用企業 | Global European Pharmaceutical Company |
| 勤務地 | 東京都 23区 |
| 雇用形態 | 正社員 |
| 給与 | 経験考慮の上、応相談 |
Main Responsibilities
Support the development and execution of the Japan Medical Plan, providing scientific input for medical content and contributing to cross-functional initiatives including regulatory interactions and lifecycle planning.
Lead and support medical communication activities ? including publication planning, congress and symposia participation, and advisory board presentations ? to advance scientific exchange with the medical community.
Build and nurture relationships with key opinion leaders and scientific societies, collecting and sharing medical insights to inform strategy and strengthen our presence in the therapeutic space.
Plan and execute company-sponsored clinical studies and externally sponsored research collaborations, including post-approval studies and Investigator-Sponsored Studies, to generate meaningful real-world evidence.
Analyze real-world data in collaboration with internal and external experts to deepen understanding of the disease space and support evidence-based decision-making.
Partner with Medical Science Liaisons and global medical teams to develop field strategies that address the evolving needs of healthcare professionals and patients.
Ensure all medical activities are conducted with the highest standards of scientific integrity and in full compliance with applicable regulations and guidelines.
Employee Benefits:
Employment Type: Full time employee
Office Location: Central Tokyo
Working Style: Hybrid and super-flex time
Salary Budget: Up to 15mil
Welfare and Benefits: Available. Highly comprehensive plan will be shared during offer process.
Interview Steps: 2
Working Language: Japanese and English
| 職務経験 | 3年以上 |
| キャリアレベル | 中途経験者レベル |
| 英語レベル | ビジネス会話レベル |
| 日本語レベル | ビジネス会話レベル |
| 最終学歴 | 大学卒: 学士号 |
| 現在のビザ | 日本での就労許可が必要です |
About you
Experience: Background in medical affairs, R&D, or clinical research within the pharmaceutical industry, including experience in an MSL or Medical Advisor/Medical Manager capacity; prior involvement in clinical trial or study management is a strong advantage.
Technical skills: Strong scientific acumen in a relevant therapeutic area; ability to critically analyze and interpret clinical and real-world data; experience in medical writing and publication activities.
Soft skills: Strategic thinking with the ability to operate independently while collaborating effectively across functions; strong interpersonal skills with a genuine commitment to serving healthcare professional needs; approachable, adaptable, and a clear communicator.
Education: Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant medical or scientific discipline, or an equivalent combination of education and experience.
Languages: Fluent in Japanese; business-level English (reading and writing) required.
| 雇用形態 | 正社員 |
| 給与 | 経験考慮の上、応相談 |
| 業種 | その他 |