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Clinical Research Associate / 臨床開発モニター(東京・大阪・在宅可)
ParexelTokyo, Japan30+日前
職務内容の詳細
When our values align, there's no limit to what we can achieve.
- GCP(Good Clinical Practice)、治験実施計画書、SOP(Standard Operating Procedure)に則って治験が進んでいるかを確認
- SDV : Source Data Verification)を実施し、症例報告書（CRF : Case Report Form)とカルテ等が一致しているかを照合し、回収
- IRB (Institutional Review Board)への文書提出及び手続き
Job Qualifications :
CRA経験（経験年数1年以上） ※経験領域・疾患は問いません
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Research Associate • Tokyo, Japan
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