40FspCra
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Job Summary
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
- 治験を実施する医療機関や医師の選定
- 治験の依頼契約
- 治験薬の搬入及び回収
- モニタリング 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
- 直接閲覧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
- 医療機関における保管必須文書が適切に保管されているか確認
- モニタリング報告書作成
- 治験の終了手続き など
About Company
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more
