Iqvia Services / Clinical Operations / Cra(経験者 )

IQVIA

Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

<担当業務>
製薬メーカー・医療機器メーカーから受託しているプロジェクトの治験実施計画書に基づき、治験チームリーダーが作成するモニタリング管理計画書(CMP)に従ってモニタリング業務を実施する。

<勤務地>
品川本社/大阪事業所/福岡事業所
 

<必須>
・CRA経験2年以上(GCP下での臨床試験の経験)
・単独で施設訪問ができる

<経験があれば尚可>
・グローバル試験の経験
・大学病院やがんセンター等の担当経験
・監査又は実施調査の経験必須
・リーダー経験あり(若手の指導・育成)


Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice


Tokyo/Osaka/Fukuoka


・At least, 2 years experience as CRA
・Knowledge of GCP
・Completed the Sign-Off
・Able to visit the site individually
・Fluent in Japanese

<Preferred>
・Global project experience
・Performed at the University hospital or Oncology hospital
・Acted as a mentor for new clinical staff

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™



Job ID: R1054692
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Confirmed 14 hours ago. Posted 6 days ago.

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