Skip Navigation

【6月入社限定】未経験CRA(東京・大阪)

Tokyo, Tokyo, Japan Date posted 02/26/2025 Job ID R0000031486

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

【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

※入社後研修※

入社1か月目は座学研修(GCPやCRAについて説明)

その後入社2か月目~3カ月目でOJTで先輩の業務を一緒にご対応頂きながら、

CRAの社内モニター認定を受けて頂き、合格後CRAとして業務を開始頂きます。

なお、先に内勤業務にアサインされる可能性もございます。

【応募条件】

以下条件にすべて該当する方

■以下職種で1年以上の実務経験を有する方

CRC / SMA / 看護師 / 臨床検査技師 /  臨床工学技師 /薬剤師 / 獣医師 / MR 等

 ※CRAで医師主導治験のみの経験をお持ちの方や臨床研究のご経験をお持ちの方からの応募も歓迎します

■英語に対して苦手意識を持っていないこと

■2025年6月1日付に入社できる方

【このような方を求めています!】

●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

●フットワークよく出張を楽しめる方

オンライン会社説明会も毎月実施しております。

申込はこちらからお願いします

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.

@* *@