Manage and execute communication strategies for Asia, aligning with global business priorities. Represent the Global Communications team and ensure consistent messaging across the region. Client Details Our client is a globally recognized leader in supply chain
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
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
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
* 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
* 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 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
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
About the Team OpenAI’s mission is to ensure that general-purpose artificial intelligence benefits all of humanity. Our Communications team includes PR/media relations, employee communications, events, design, and other external-facing functions. This team’s ethos is to support OpenAIs mission
About Four Seasons: Four Seasons is powered by our people. We are a collective of individuals who crave to become better, to push ourselves to new heights and to treat each other as we wish to
This is what you will do: Associate Director, Regulatory Affairs is responsible for overall pharmaceutical affairs associated with obtaining pharmaceutical product approval. The duties include complying with Japan pharmaceutical affairs act, developing good relations with the regulatory
Your Job The Group Product Manager preferred to be functioned both independently as well as in a team. Responsible for product portfolio P&L in key markets as wells as driving growth with new products / markets,
Your Job The Product Manager preferred to be functioned both independently as well as in a team. RResponsible for product development and its profitability.P&L in key markets as wells as driving growth with new products /
Overview: The specialist/senior specialist, public relations is responsible for identifying opportunities to execute internal and external corporate public relations programs to enhance Abiomeds mission of heart recovery, sustain its Patients First culture, and contribute to continuous business growth. This
