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Clinical Research Associate / 臨床開発モニター(Boston Career Forum 2024)

Tokyo, Tokyo, Japan Date posted 08/30/2024 Job ID R0000026942

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.

As a CRA at Parexel, you‘ll be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter—people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.

Success Profile

Check out the top traits we’re looking for and see if you have the right mix.

  • Innovative
  • Problem-Solver
  • Communicator
  • Tech-Savvy
  • Confident
  • Independent
  • "The last 4.5 years I had a steep learning curve and I am still learning via on-the-job challenges and solid management feedback. Next to my personal growth, I also enjoy our open atmosphere and the great collegiality."

    Stefanie – Sr Clinical Research Associate

Rewards

  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Compensation

    Competitive salaries and bonus structure based on individual metrics.

Responsibilities

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遂行します。

【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

【求める人物像】

  • 倫理観をもって取り組める方
  • 協調性をもって取り組める方
  • 社内外の多くの人々とコミュニケーションすることが好きな方
  • 自ら考え、自ら行動できる方
  • 新薬を世に出したいという情熱をもって取り組める方
  • グローバルなフィールドで活躍したい方


【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(希望制)

【応募条件必須】

  • Bachelor's Degree以上の学位を取得した方、または取得見込みの方
  • 理工系専攻の方   ※Biology, Chemistry, Public Health, Psychology, Nursing, Pharmaceutical Sciencesなどの専攻の方歓迎
  • 2025年4月もしくは2025年10月入社が可能な方

【選考方法】

本フォームより応募いただいたのちに、ボストンキャリアフォーラム2024を通してご応募いただきます。

※すでに ボストンキャリアフォーラム2024 でご応募いただいている方は、こちらからご応募いただく必要はございません。

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