Job Responsibilities:
? Making arrangement for Investigator Meetings & Study Team Meetings including taking minutes.
安排和協(xié)調研究者會議及項目組會議事務,包括會議記錄等.
? Assist with the Ethics / Regulatory Submissions and keep a track of submissions & ?study.
協(xié)助倫理和法規(guī)的遞交工作,跟蹤遞交與批復的記錄
? Preparing copies of Protocols, Investigator Brochures akeeping track and re-ordering supplies.
準備研究方案,研究者手冊和病例報告表,跟蹤物資的申請、發(fā)放與保存記錄
? Setting up and maintenance of the Trial Master Files (TMF) or Electronic filing systemsSite File (IF)
建立并管理試驗主文件夾及電子文檔保存系統(tǒng),協(xié)助研究者文件夾的設立
? Preparing essential clinical trial documentation, distributing, tracking and filing of doments on return.