■ 職務内容 / Job Description Drive development and execution of external communications strategy to drive a corporate reputation and advance science and therapeutic area leadership of AZKK. Leads a team of external communication managers and specialists covering corporate
Minimum qualifications: Bachelors degree or equivalent practical experience. 8 years of industry experience in advertising, consultative sales, business development, or IT, or 6 years of experience with an advanced degree. Ability to communicate in English and
Minimum qualifications: Bachelors degree or equivalent practical experience. 8 years of industry experience in advertising, consultative sales, business development, or IT, or 6 years of experience with an advanced degree. Experience in digital marketing and with
Join a fast-growing company as an Administrative Assistant, playing a key role in business growth. Work closely with the Japan Manager to ensure organizational efficiency and effectiveness. Client Details Our client is a dynamic and rapidly
As the TA Partner for the business unit you will be in charge of, you will be responsible for full-cycle recruitment for Japan. This role will be focusing on more senior candidates and quality vs volume
Reporting to the Hinseki and lead in handling and handling QMS as well as other quality activities. Ensure effective compliance for companys products Client Details * Global medical device company specializing in the oncology area *
As a TA Partner you will be working with the rest of the TA team and the hiring managers for positions based in Japan. Client Details The client is a multinational healthcare company with a diverse
* Create and lead Evidence Generation Plan * X-functional position understanding strategies of Medical / Commercial / R&D Client Details * Global pharmaceutical company * Pioneer and Leader in RWE, observational research study design and execution
The Senior Clinical Research Specialist is responsible for leading and managing clinical trials and post-market studies in compliance with regulatory requirements. This role involves overseeing trial operations, coordinating with internal and external stakeholders, and ensuring data integrity
* Lead and project management of the following studies: - CSS (Company-led research) - IIS (Doctor-led research) - Collaborative study - Including oversight of external CRO Client Details * Leading global CRO business, with rich project pipeline
* Key External Experts (KEEs)やヘルスケアプロフェッショナル（HCP）との医療・科学情報のピアツーピア交流を通じてビジネス目標を達成する * 内部関係者と協力してビジネス目標を達成するための戦略を策定し実行する Client Details * ヨーロッパ製薬メーカー Description * Key External Expertエンゲージメント: 医療の洞察を特定し、チームにフィードバックして将来の医療/商業戦略を策定する * 研究および医療教育: 研究者主導の研究についてのディスカッションに対応し、これを内部プロセスでサポートする * 内部のX-クショナルコラボレーション: 顧客エンゲージメント計画プロセスに意見を提供し、医療および科学的な信頼性を確保し、競争力のある製品差別化のためにデータを最適に活用する * 医療コンプライアンス: すべての顧客とのやり取りが国の行動規範、法的および倫理的基準、その他すべての関連するポリシーおよび内部ガイドラインに準拠していることを確認する Profile * MSL経験（MRもOK） * ５年以上製薬メーカー経験 Job Offer * メディカルアフェアーズでは珍しいキャリア * インターナショナルなノウハウを身につけ、グローバルなコミュニケーションを体験する機会 Page
Lead in GQP QA operational activities for the business for company products. Ensure effective compliance, continuous improvement activities, and overall quality processes. Client Details * Global Pharmaceutical company specializing in generics, biosimiilars, APIs, and new products
Be responsible for monthly, quarterly and annual closing and support the creation of financial reports for internal use. Coordinate with external auditing firms for audits (accounting audits, J-SOX). Client Details A cutting-edge equipment manufacturing company. A global
Take lead in CMC RA activities for the business in regulatory strategy/maintenance to obtain and maintain regulatory approval. Contribute and support the CMC RA organization both domestically and overseas members Client Details * Global Pharmaceutical company
Be part of a top 10 Global CRO thats entering the Japan market as a first member. Lead in RA activities to submit clinical trial documents to obtain approval. Client Details * Top 10 global CRO
Take lead in quality activities to ensure effective compliance. Manage QMS and other quality claims. Client Details * Global pharmaceutical company specializing in innovative treatment for oncology, urology, and auto-immune areas. * Rich development pipeline for
Work Flexibility: Hybrid or Onsite Basic purpose of role/Why the job exists: The Transport Product Engineer is responsible for the day to day product support and technical aspects of customer product enquiries. In partnership with the
About SiFive As the pioneers who introduced RISC-V to the world, SiFive is transforming the future of compute by bringing the limitless potential of RISC-V to the highest performance and most data-intensive applications in the world.
Welcome to Warner Bros. Discovery… the stuff dreams are made of. Who We Are… When we say, “the stuff dreams are made of,” we’re not just referring to the world of wizards, dragons and superheroes, or
Overview News can change the world, save lives, and bring us all closer together through empathy and understanding - but not if it isn’t read. Out of the hundreds of millions of articles and posts, how
