At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
日本に120年以上の歴史を持つグローバル金融機関、シティグループ証券株式会社（東京・大手町）は、オペレーション部門のリファレンス・データ・アナリストを募集しています。 If you have native-level Japanese reading proficiency and advanced English communication skills, this Reference Data Analyst role at Citi offers the opportunity to manage and improve the integrity of critical security, pricing, and account data
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put
Compliance, Regulatory Affairs and Resources, Regional Country Compliance, Vice President, Tokyo Responsibilities The Regional Country Compliance (“RCC”) team in Tokyo Compliance is responsible for helping ensure that the firm manages and responds to regulatory inquiries, examinations and regulatory filings.
HSBC Asset Management (“AM”) Product Group is responsible for the strategic and commercial development of AM Product manufacturing capabilities including Development, Management, Governance, Support and Mandate delivery across all Global Markets. The product function is expected
Job Description Summary: Job Description We deliver enhanced consumer protection and global advocacy to ensure our business maintains license to operate in all markets. This role implements and develops our global regulatory harmonization initiatives on food additives
求人内容 Summary of Job Description: Manager, Regulatory Affairs (RA) Therapeutic Area (TA) Group, Regulatory Affairs Japan, is accountable for executing regulatory activities within assigned projects or therapeutic areas, acting as a core member of project teams. This role ensures
企業概要 About AbbVie 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
Job Overview: Collaborate with Site Readiness stakeholders and cross-functional teams to ensure client-centric delivery in a matrix organization. Provide oversight and accountability for Regulatory Authority (RA) submissions and coordinate, as applicable, activities related to Independent Review Board
Job Overview: Works directly with GRA Leadership, GRA personnel, and client development teams to support the development and execution of regulatory strategies across all stages of product development. Candidate will collaborate with senior regulatory strategists and cross-functional subject
求人内容 Summary of Job Description: Manager, Regulatory Affairs (RA) Therapeutic Area (TA) Group, Regulatory Affairs Japan, is accountable for executing regulatory activities within assigned projects or therapeutic areas, acting as a core member of project teams. This role ensures
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
Are you interested in cross-border projects and communications? Would you like to work for a global business Legal Technology and Compliance? About the Role LexisNexis is building market-leading solutions that help organizations manage regulatory obligations, monitor regulatory change,
Are you interested in cross-border projects and communications? Would you like to work for a global business Legal Technology and Compliance? About the Role LexisNexis is building market-leading solutions that help organizations manage regulatory obligations, monitor regulatory change,
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Regulatory Affairs to join our Regulatory Affairs team, supporting our Japan business
Job Overview: Responsible for actively contributing to the development and implementation of regulatory strategy for specific projects, serving as the regulatory representative from Japan on relevant project teams, and serving as the regulatory contact with relevant regulatory authorities, as appropriate.
メルクと一緒に、あなたの力を発揮しよう！ 冒険、限界への挑戦、そして発見に焦がれるあなたへ。あなたの大志を、メルクで羽ばたかせましょう！科学とテクノロジーを駆使したイノベーションに情熱を注ぐメルクのスタッフは世界中で活躍中です。ヘルスケア、生命科学、エレクトロニクスの分野で、メルクのソリューションは人々の暮らしをますます豊かなものにしています。あなたとメルクの力を合わせて、大きな夢を抱きましょう。メルクは、人、顧客、患者、そしてこの地球という惑星が共存する豊かな世界の構築に情熱を注いでいます。このためメルクでは、好奇心にあふれた人材を募集中です。メルクと一緒に、想像を超えた世界を開拓しませんか？ 患者さんのためにひとつになって団結し、生命の誕生、QOLの向上、命をつなぐサポートをすることか、ヘルスケアにおける私たちの目的です。私たちは、腫瘍学、神経学、不妊治療などの疾患領域において、医薬品、インテリジェント装置、革新的技術を開発します。私たちのチームは、人生のすべてのステージで患者さんを助けるために、情熱と執拗な好奇心を持って6大陸全体で協力して働いています。ヘルスケアチームに入ることは、多様的で包含的、そして柔軟な職場文化の一部となることです。世界中で個人的な能力開発とキャリアアップの素晴らしいチャンスが待ち受けています。 Specific Job Description Key Accountabilities As a subject matter expert, the Clinical Research Scientist (CRS) partners with the Medical Lead to provide scientific, clinical, strategic, and operational input to an early or late-stage
Senior Growth Manager - Japan About Tazapay Tazapay is a cross border payment service provider. They offer local collections via local payment methods, virtual accounts and cards in over 70 markets. The merchant does not need
＊Position Summary 企業のサステナビリティ情報開示やESG関連業務の支援を担当いただきます。クライアントの情報開示対応、調査・分析、資料作成等を通じて、企業のサステナビリティ推進をサポートしていただきます。 ＊Key Responsibilities ・サステナビリティ開示業務（有価証券報告書、統合報告書、サステナビリティレポート等）の支援 ・CSRD、ISSB、TCFD等の開示フレームワークに関する調査・分析 ・ESG関連データの収集・整理・分析 ・クライアント向け資料や提案書の作成支援 ・プロジェクトマネージャー・シニアコンサルタントの業務サポート ・その他、企業のサステナビリティ推進に関するコンサルティング業務支援 ＊Requirements Must Have ・大卒以上 ・1～３年程度の実務経験 ・ビジネスレベルの英語力 以下いずれかの経験 ・サステナビリティ／ESG関連開示業務 ・統合報告書、有価証券報告書等の作成・支援 ・IR、CSR、サステナビリティ推進業務 ・日本語での高度なコミュニケーション能力 Preferred ・CSCC領域に関する業務経験 気候変動/カーボンマネジメント/脱炭素戦略/Scope1・2・3算定 TCFD対応 ・コンサルティングファームでの業務経験 ＊Ideal Candidate ・サステナビリティ分野への強い関心をお持ちの方 ・自ら学びながら業務を推進できる方 ・データ分析や文書作成を丁寧に行える方 ・チームワークを重視できる方 Why This Role Matters
Job Description SummaryAs a Manager, Global Clinical Supply Group, you will play a critical role in ensuring uninterrupted clinical trial supply across Japan. Working closely with global and local stakeholders, you will develop and execute clinical