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【未経験者採用:2月入社】Clinical Research Associate / 臨床開発モニター(東京・大阪・神戸)

Japan, Remote Date posted 08/10/2022 Job ID 84685BR

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

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

パレクセルは世界有数のグローバルCROの一社で、数多くの製薬メーカーのお客様からプロジェクトを受託しております。事業拡大に伴い、プロジェクトメンバーの一員として、モニタリング業務を遂行下さる方を求めております。未経験から新薬開発にチャレンジしたい方からのご応募をお待ちしております。

【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 等

【応募条件】

医療業界での勤務経験1年以上お持ちの方
例:薬剤師、看護師、臨床検査技師、MR、CRC 等

*英語力:読み書き中級以上

*2月1日付入社が可能な方

会社のことや仕事内容をもう少し詳しく知りたい、だけでもかまいませんので、少しでもご興味をもたれましたら、まずはご相談ください。

オンライン説明会も毎週実施中です。お気軽にご参加ください。


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