When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
【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
【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
What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:
• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.
We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
