企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across
Job Description Summary -Contributes, with appropriate oversight, to all relevant aspects of global clinical trial(s) activities to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core
Career Category Clinical Job Description Purpose: Provide clinical site contracting services to clinical study teams to support study start up and conduct activities Context: Amgen K.K. office Reports to CTOM (Clinical Trial Oversight Manager) Responsibilities Manage
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
【職種】治験関連 モニタリング Study Associateとして、Regional Study Managerのサポートをし、主に日本のクリニカルオペレーション業務を行う。 ●モニタリング報告書レビュー ●安全性情報伝達 ●施設文書レビュー（ICF、費用、契約書） ●JRCT登録/更新 ●臨床試験情報更新（毎月） ●治験変更届対応 ●Sponsor functional QC ●TMF保管 ●文書トラッカー管理（及びInspection readiness関連アクティビティ） ●公印請求対応 ●各種システムアクセス権の管理・申請 ●SIV、Pre-IRB、IRB同席 ●IM 準備 ●CRO/Vendorの手順書、資料のレビュー 品川（品川区） 08:45 〜 17:30（休憩12:00 から 60分間） 【派遣先について】 業種：メーカー関連 【派遣会社】株式会社アールピーエム 残業代別途支給 交通費支給（当社規定による） 社保完備 産休・育児休暇制度
Job Overview At a global level, drive Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines to develop the informed consent form (ICF), including during
