Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
【2027年新卒】オファー承諾者専用
Job ID R0000038755 Tokyo, Tokyo, Japanこちらは、2027年新卒採用でオファーを承諾いただけた方の専用ポジションです
Clinical Research Associate/臨床開発モニター
臨床開発モニターは、新薬を世に出すために欠かせない重要な役割を担っています。世界中の患者さんに貢献できる大変やりがいのある仕事で、以下のような業務を行います。
【業務内容】
・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、治験実施計画書、SOPに則って治験が進んでいるかを確認
・直接閲覧(SDV)を実施し、症例報告書とカルテ等が一致しているかを照合し、回収
・IRB(治験審査委員会)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
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