エージェント求人

Senior Clinical Research Associate（Oncology)

600~900万

アストラゼネカ株式会社

大阪府大阪市, 東京都港区

募集要項選考・企業概要

職務内容

職種

医薬品CRA

仕事内容

Monitor is responsible to ensure that the trial is conducted and documented properly by carrying out the following activities when relevant and necessary to the trial and the trial site in order to verify that: ・The rights and well-being of human subjects are protected. ・The reported trial data are accurate, complete, and verifiable from source documents. ・The conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP, and with applicable regulatory requirement(s).

求める能力・経験

【経験 / Experience】＜必須 / Mandatory＞ • At least 3 years of CRA experience. • Demonstrated leadership capability in a team environment successfully. • Negotiated some complicated issues and/or requirements with site staff. • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities ＜歓迎 / Nice to have＞ • Preferred experience to collaborate with external partners. • Performed monitoring activities from qualification visit to closure visit as a CRA.