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| Hiring Company | 非公開 |
| Location | Tokyo - 23 Wards |
| Job Type | Permanent Full-time |
| Salary | 6.5 million yen ~ 9 million yen |
【求人No NJB2383495】
【職務内容】
・臨床開発計画の立案
・規制当局対応(FDA、EMA等の海外当局含む)
・治験プロトコールの立案/作成/メンテナンス
・承認申請資料の作成
・他部門(非臨床部門、薬事部門、クリニカルオペレーション部門、DM/統計解析、PV等)との連携 など
| Minimum Experience Level | No experience |
| Career Level | Mid Career |
| Minimum English Level | Business Level |
| Minimum Japanese Level | Native |
| Minimum Education Level | Bachelor's Degree |
| Visa Status | Permission to work in Japan required |
【必須要件】
・生命科学分野の学位を有する
・治験プロトコール作成、治験管理、総括報告書の作成経験(経験目安:3年以上)
・ビジネスレベルの英語力(グローバルメンバーと会議でディスカッション可能なレベル)
・GCPに関する基本的な理解
| Job Type | Permanent Full-time |
| Salary | 6.5 million yen ~ 9 million yen |
| Work Hours | 09:00 ~ 18:00 |
| Holidays | 詳細は求人ご紹介時にご案内いたします。 |
| Industry | Pharmaceutical |