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Hiring Company | 非公開 |
Location | Tokyo - 23 Wards |
Job Type | Permanent Full-time |
Salary | 5.5 million yen ~ 9 million yen |
【求人No NJB2081896】
・関連部署及び外部業者との調整、進捗及びスケジュール管理
・臨床開発関連文書作成 (試験実施計画書、同意説明文書、治験薬概要書等、治験総括報告書、CTD等)
・開発関連文書作成時のQC 等
Minimum Experience Level | No experience |
Career Level | Mid Career |
Minimum English Level | Business Level |
Minimum Japanese Level | Native |
Minimum Education Level | Technical/Vocational College |
Visa Status | Permission to work in Japan required |
【必須】
・製薬企業あるいは製薬関連のCROでのメディカルライティング業務の経験3年以上
⇒CTD(臨床)を作成した経験は必須。
・TOEIC600点以上または、同等の英語力を有する方
Job Type | Permanent Full-time |
Salary | 5.5 million yen ~ 9 million yen |
Work Hours | 09:00 ~ 18:00 |
Holidays | 【有給休暇】初年度 10日 4か月目から 【休日】完全週休二日制 夏季休暇 年末年始 |
Industry | Contract Research Organization |
Company Type | International Company |