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Mission1. 日本における臨床試験を開始するにあたり,PMDA相談資料の作成,治験薬概要書の作成等を適切に遂行する役割を担う2. 日本における承認申請業務において,グローバルチームと連携してCTDを作成し,PMDAからの照会事項へ適切に対応する役割を担う。3....

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