Company Description PSI is an award-winning full-service CRO, bringing together more than 2,700 dynamic and knowledgeable individuals working to help impact the future of medicine in more than 60 countries around the world. We support pharmaceutical,
JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you
Basic Purpose of the job: Prepare and finalize non-clinical pharmacology documents for PMDA submission. Be representative for key interactions with PMDA in terms of non-clinical pharmacology, aiming for commercial success of Boehringers products Make value propositions for all
Project Manager/ BioReliance® Contract Testing Services, Life Science Services Location: Tokyo Report to: Manager in Japan Direct report: 0 ABOUT BioReliance® Contract Testing Services BioReliance® Testing Services provides testing and manufacturing services to pharmaceutical and biopharmaceutical companies that span
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to
About Welo Life Sciences Welo Life Sciences, a Welo Global brand, is a specialized language and technology partner serving pharmaceutical, CRO, and medical device organizations operating in regulated global markets. We deliver regulator-ready translation, linguistic validation,
Job Purpose: · Drives and deliver pipeline projects within timeline, budget and resource while fostering cross-functional collaboration in and beyond project teams. · Serve as the most reliable and trusted partner for leaders, enabling timely and high-quality decision-making,
About Welo Life Sciences Welo Life Sciences, a Welo Global brand, is a specialized language and technology partner serving pharmaceutical, CRO, and medical device organizations operating in regulated global markets. We deliver regulator-ready translation, linguistic validation,
General Information Job Advert Title: Clinical Trial Manager Location: Tokyo, Nihonbashi Division: Early Development and Translational Science Employment Class: Permanent Description 【About Astellas】 Astellas is a global life sciences company committed to turning innovative science into VALUE for
Project Manger, FSA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the
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.
MAIN REPONSIBILITIES / DUTIES JOB POSITION PURPOSE The MAS roles are hybrid in responsibilities. Specific roles in teams can vary between 80% field with 20% head office activity to 80% head office activity with 20% field
Company Description Sirtex Medical is a global leader in healthcare, with offices in the U.S., Australia, Germany, and Singapore, dedicated to improving patient outcomes. Our mission is to be at the forefront of minimally invasive cancer
English Follows Japanese: 募集職種：プロダクト開発サポートマネージャー（日本担当） 日本のヘルスケアの未来を共に創り上げる、革新的で前向きなプロダクトマネジメントのプロフェッショナルを求めています。 次世代の医療従事者を支えるデジタルプロダクトを開発したい方 グローバルな情報・アナリティクス企業でキャリアを築きたい方 ぜひ、私たちと一緒にヘルスケアの未来を形にしませんか。 ■ チームについて Elsevier Health は、医療従事者・教育者・学生に向けて、エビデンスに基づく情報と革新的なデジタルソリューションを提供する世界的リーダーです。 臨床意思決定支援、専門職向け教育、医学教育、ヘルスケアアナリティクスなど、多岐にわたるソリューションを通じて、医療の質向上と患者アウトカムの改善に貢献しています。 ■ 職務内容 本ポジションでは、強い技術的知見を持ち、プロダクト開発を多面的に支援できるプロダクト開発サポートマネージャーを募集します。 新規デジタルプロダクトの企画・検討・実行、既存プロダクトの戦略的拡張など、幅広い領域でプロダクトマネジメントチームを支える重要な役割です。 プロダクト開発サポートマネージャーは Clinical Solutions Japan のディレクターにレポートし、コンテンツチーム、エンジニア、その他ステークホルダーと密接に連携しながら、アイデアの創出から開発・デリバリーまでを推進します。 ■ 主な業務内容 ・プロダクトのディスカバリーおよび開発フェーズにおける技術的・実行面でのサポート ・新規プロダクトアイデアや機能拡張案の収集・整理・分類、および顧客ニーズや事業成長との整合性評価 ・新規アイデアや改善項目に関する English Version: Are you an innovative and forward-thinking product
LOCATION: Tokyo, Japan POSITION SUMMARY: We are seeking a highly motivated and strategic Product Manager to support the commercial launch and ongoing growth of Signatera in Japan. This role will work closely with the U.S.-based Global Product
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development,
JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you
Department:Regulatory CMC Japan Report to:Head,Non-clinical & CMC Dev 1. Act as a key person to coordinate CMC and/or regulatory science issues between global and Japan so that appropriate solutions are provided 2. Be responsible for preparation of
Key Accountabilities: Develop and execute regulatory affairs (RA) activities from the development to the life cycle management, with collaborative with global and Japan stakeholders. Regulatory Affairs Manager will focus on some of the following activities in Regulatory
Responsibilities will include, but are not limited to the following: Provide leadership and build an exceptional team to manage the patient scheduling system and process Support hiring, training, coaching, and onboarding activities related to patient scheduling,