国内外のTrial Master File (TMF) の管理を通じて臨床試験のQualityに責任を持つ
・TMF管理全般 (SOP/Manual管理含む)
・eTMF System仕様変更
・手順書,Specificationの作成
・TMF Qulity Review
・TMFに関するCRO Oversight
・信頼性調査準備/対応
Responsible for driving global and regional clinical trials
- TMF Management including SOP/Manual updates
- eTMF System Change Controll
- Create and optimize TMF plan and specifications
- Qulity Review of TMF
- CRO Oversight
- Inspection readiness and support"