Clinical Research Associate Location: Nakano, Tokyo, Japan Function: Clinical Sciences, Boston Scientific Japan Purpose Statement The Clinical Research...
機器) -グローバル試験の経験不問 - GCP(Good Clinical Practice) の知識 - 中級レベル以上の英語力(読み書き) Labcorpの成功は、チームメンバーのさらなる成長とキャリアデベロップメントの機会を提供します。 Labcorpでは新薬による奇跡「ミラクル」を現実するためのお手伝いをしています。すば...
An In-house Clinical Research Associate will work closely with the Clinical Research Associates (CRAs) by providing centralized support to regional team...
At Labcorp, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission ...
審査委員会への手続き、治験関連資料の翻訳、各規制当局への告知・連絡、有害事象の報告 要件: - 学士資格（薬学、医学、生物科学、看護などの分野尚可） - 臨床開発モニターとしての1年以上の経験(医薬品、医療機器) - GCP(Good Clinical Practice) の知識 - 中級レベル以上の英語力(読み書き) Labcorpの成...
Purpose: To manage all site related contracting and budget negotiations and site payments Context: Amgen K.K. office Reports to CTOM (Clinical Trial Oversight...
仕事内容： ■海外学会対応 ■研究助成/教育助成プログラムの立上げ、運営 ・医療従事者からの申請受付、問い合わせ対応 ・コミッティなど必要な会議のセットアップ、運営 ・社内ステークホルダーとの連絡、調整 ■プロクターマネジメント ・海外施設や医師との契約業務 ・海外担当者との連絡業務 ・国内、海外医師の宿泊・交通手配業...
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, India...
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, India...
Job Purpose: This position provides oversight of clinical research sites compliance with Good Clinical Practices, ISO-14155 and applicable laws and regulations...
We are seeking a talented Clinical Trial Manager (CTM) to join us. This is a virtual role that may be based anywhere in Japan. The CTM will work closely with...
Your responsibilities include, but not limited to: -Ensures the timely collection, monitoring, and reporting of Quality Key Performance Indicators (KPIs) for ma...
9.4 billion spend on Research and Development. That commitment resulted in 24 major regulatory approvals in 2019 in the US, EU, Japan and China. Your Responsibi...
9.4 billion spend on Research and Development. That commitment resulted in 24 major regulatory approvals in 2019 in the US, EU, Japan and China. Major Accountab...
1. Act as PHAD-Japan representative of TRD-Japan sub team for development and submission in Japan - Review and prepare protocols & reports for method validation...
As part of Sandoz Japan development team, this role is critical in future Sandoz Japan growth by contributing development activity support and regulatory activi...
Your responsibilities include, but not limited to: -Ensures the timely collection, monitoring, and reporting of Quality Key Performance Indicators (KPIs) for ma...
9.4 billion spend on Research and Development. That commitment resulted in 24 major regulatory approvals in 2019 in the US, EU, Japan and China. Your Responsibi...
Your responsibilities include, but not limited to: -Ensures the timely collection, monitoring, and reporting of Quality Key Performance Indicators (KPIs) for ma...
9.4 billion spend on Research and Development. That commitment resulted in 24 major regulatory approvals in 2019 in the US, EU, Japan and China. Major Accountab...
