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FSP Clinical Research Associate / FSP 臨床開発モニター(東京・大阪・神戸)

Tokyo, Tokyo, Japan Date posted 08/12/2022 Job ID R0000001132

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. Explore opportunities within our core Clinical Development, Biotech, or Functional Service Provider (FSP) teams below.

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


  • 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.



パレクセルFSP (Function Service Provision)で臨床開発業務に就くことは、CROとスポンサー両方の経験を統合させ、より付加価値の高いキャリアを構築する機会となります。世界をリードするCROパレクセルの一員でありながら、バイオ医薬品メーカーのお客様チームのメンバーとして経験を重ねることで、臨床開発のプロフェッショナルとして更に成長することができます。


  • 治験を実施する医療機関や医師の選定

  • 治験の依頼

  • 治験中のモニタリング

  • 症例報告書の回収

  • 副作用情報の対応など


  • がん領域

  • 中枢神経系

  • 心血管および代謝性疾患

  • 感染症


CRA グローバルスタディ、オンコロジー領域経験1年以上経験者

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