転職・求人情報の詳細をご覧になる場合は会員登録（無料）が必要です
| 部署・役職名 | Senior Regulatory Affairs Manager |
|---|---|
| 職種 | |
| 業種 | |
| 勤務地 | |
| 仕事内容 |
You will lead the team that works to get new medicines approved in Japan. Your job is to talk with Japanese health officials and manage the rules for drugs from the new development stage to after they are sold. You will also help teach and manage the team members. Responsibilities － Lead all discussions with Japanese health agencies. － Lead the strategy and applications for new drug approvals. － Manage all rule changes for medicines already being sold. － Review and approve advertising materials to make sure they follow the rules. － Lead the team and teach new staff members. |
| 応募資格 |
【必須（MUST）】 － 5＋ years of experience in drug development or managing drug rules.－ Experience working well with global and local teams. － Fluen－ t Japanese with business－level English. － Strong leader who is good at making plans and managing risks. |
| 受動喫煙対策 | 屋内禁煙 |
| 更新日 | 2025/11/17 |
| 求人番号 | 6127851 |
採用企業情報
- 企業名は会員のみ表示されます
- 会社規模101-500人
この求人の取り扱い担当者
-
- ?
- ヘッドハンターの氏名は会員のみ表示されます
会社名は会員のみ表示されます
-
- メディカル
-
転職・求人情報の詳細をご覧になる場合は会員登録（無料）が必要です