Skip Navigation

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.

【直接応募で一時金40万円】FSP派遣モデルCRA

Job ID R0000045384 Tokyo, Tokyo, Japan
職務概要
臨床開発モニターとしての経験を活かし、製薬会社様の臨床開発部門のCRAとしてプロジェクトに携わっていただきます。
※本職務は、外部就労のオポチュニティーが発生した際に、優先的にアサインを検討させていただく職務です。そのため、オポチュニティーがないときは、パレクセルのFSP部門でCRAとして勤務していただきます。

以下は、パレクセルのCRAの職務内容です
  • 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

【取り扱う疾患領域】
•がん、中枢神経、心臓血管、感染症、希少疾患など幅広いなど──取り扱う領域は多岐にわたっています

【その他の情報】
•配属部署: 臨床開発部
•配属オフィス: 東京・大阪(一部在宅可) ※外部就労時は製薬会社様のオフィス

応募条件:
【必須】
CRA経験(経験年数1年以上) ※経験領域・疾患は問いません

【その他】
•グローバル試験や、オンコロジー領域に挑戦したい方
•製薬会社様でCRAとして勤務してみたい方

【求める人物像】
 •チームワークを大切にできる方
  •他者と良好な関係を築くのが得意な方
  •的確な状況把握と臨機応変な判断力

こちらから外部就労をしたパレクセルのCRAの動画をご視聴いただけます。

※本採用サイトからの直接応募で入社一時金40万円支給対象となります
詳しくは、こちらをご確認ください。

Join our Talent Community

Welcome to the Parexel Talent Community! Sign up below and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events.

Recently Viewed Jobs

You have not recently viewed any jobs

View all jobs

RECRUITMENT FRAUD ALERT

It has been brought to our attention that there has been fraudulent activity by scammers attempting to represent themselves as Parexel employees or recruiters. These individuals are attempting to reach potential job seekers through online chat interviews and sending false offer letters, representing Parexel without our consent. If you’re concerned that you’ve been contacted by an unauthorized Parexel recruiter or employee, please notify Jobs@Parexel.com. You may also report suspicious fraudulent activity to your local law enforcement agency or the FBI. Thank you.

@* *@