Site Contracts Assistant/ 医薬品開発を支えるバックオフィスサポートスタッフ（東京) at Parexel

Tokyo, , Japan -

Full Time

Start Date

Immediate

Expiry Date

19 Aug, 26

Salary

0.0

Posted On

21 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Administrative Support, Document Management, Microsoft Excel, Microsoft Word, Microsoft Outlook, English Proficiency, Communication Skills, Attention to Detail, Contract Administration, Filing

Industry

Pharmaceutical Manufacturing

Description

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. 職務内容: 製薬会社の新薬開発プロジェクトを医療施設で行う際の契約締結を幅広くサポートいただく、アシスタント職です（要オフィス出社）。 ※役員等の秘書ではございません具体的な業務内容：文書の印刷、コピー、ファックス、郵送、スキャン、ファイリング契約書の押印・発送・保管管理翻訳サービスの調整／発注システムに対する問い合わせやタスクの解決文書管理プロセスの改善諸外国における文書管理のサポート等求める知識・経験：事務経験（製本経験をお持ちの方歓迎） Excel、Word、Outlook等の基本的なOAスキル正確にスピード感をもって業務を行う能力コミュニケーション能力きめ細かさビジネスレベルの英語力（読み書き必須/会話は流暢でなくても話すご意欲がある方）求める人物像コツコツとしたサポート業務が好きな方責任感と正確性を大切にできる方治験契約書という専門性のある事務にキャリアを広げたい方英語を使った仕事に前向きな方このポジションの魅力： APACのチームの一員となり、他のメンバーも様々な国におります（上司は外国人）。他の国のサポートもご担当いただくこともあり、グローバルに活躍いただくことが可能です。募集背景業務量増加に伴い、契約書管理を中心とした事務体制を強化します。安定した環境で腰を据えて働きたい方を歓迎します。 Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Responsibilities

Provide comprehensive back-office support for contract execution in pharmaceutical development projects at medical facilities. Responsibilities include document printing, scanning, filing, managing contract seals, and coordinating translation services.