JOB DESCRIPTION Job Title: Associate Director, Regulatory Affairs Japan Department / Cost Center: Regulatory – 210 Reports to (Job Title): Head of APAC Regulatory Affairs Job Code: Location: Tokyo Date Prepared: April 2024 Full-Time Part-Time Regular Temporary Exempt Non-Exempt SUMMARY
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 authority, and
Are you interested in contributing to Corporate and Investment Banking (CIB) from regulatory perspectives? As a Regulatory Reporting Operations - Associate within Market Operations, you will be responsible for 1.automation and regulatory/business/market initiated changes on Legal Ledgers and Regulatory reports owned
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical
SUMMARY Responsible and accountable for Medical Affairs strategy of Urological cancer products C ollaborates with internal and external stakeholders including key opinion leaders to develop and implement the overall M edical Affairs strategy for product lifecycle
Your days will be filled with analyzing data and building models to assist clients from across the sector in best research firm. As an associate research analyst in equity research team, you will partner closely with various
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
We’re building a relationship-oriented bank for the modern world. We need talented, passionate professionals who are dedicated to doing what’s right for our clients. At CIBC, we embrace your strengths and your ambitions, so you are
Your days will be filled analyzing data and building models to assist clients from across the sector in best research firm. As a junior analyst in equity research team, you will be working in a dynamic
At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your
Company Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North
Company Description Jobs for Humanity is collaborating with FIS Global to build an inclusive and just employment ecosystem. We support individuals coming from all walks of life. Company Name: FIS Global Job Description Position Type :
Be part of a critical member in the RA organization. Lead in RA development/strategy activities to obtain product approval for various unmet medical needs. Client Details * Global leading pharmaceutical business specialising in womens health *
Job Description Summary プロジェクト並びに新製品にかかわる従業員の安全と健康、環境を管理する役割です。HSE戦略および活動を推進し、一貫した持続的な生産性とHSEの継続的な改善を達成する責任をチーム一丸となって担います。専門知識と積極的なサポートを提供することで、HSEの標準化、簡素化、業務への統合を確実にします。またHSEの短期および長期戦略がサイトの目標に合致していることを確認し、その実施を可能にします。 Job Description 主な役割責任 新ビジネスにおけるHSE要件の完全な実施のために、適切なリソースと予算が利用可能であることを確認する。すべてのHSE規制要求事項およびその他外部からの要求事項へのコンプライアンスを実証・検証するためのシステムが整っていることを確認する。 HSEマネジメントシステムマニュアル、GOP、クラスター／サイトSOP、および支援プログラムへの適合性を確保する。ノバルティスのHSE適合性レビューや法令遵守監査、検査、地方自治体からの訪問をサポートする。 HSEリソース、プロセス、手順、プログラムの配備における効率化と標準化を推進し、価値を創造する。 現場での総合的な検査、点検、安全ウォークのプログラムの実施を推進する。プログラムを実施するための適切なアカウンタビリティを確保する。 グローバル／プラットフォーム／クラスター／サイトのHSEチーム、委員会、タスクフォースに参加する。HSE問題およびプログラムに関して、他のクラスター、サイト、機能、および／またはグローバル・エキスパート・チームとのネットワークを構築し、連携する。 必須要件 物事の本質を見極め、論理的な思考で業務を遂行することに長けている事 学歴不問 工場での製造、オペレーション、サプライチェーン環境でHSE経験をお持ちである事（３年以上が好ましい） 日本語が流暢であること。英語での読み書きが可能（翻訳ソフト使用可能）で、将来的な英語力の向上に強い意欲をお持ちの方 HSEの経験をお持ちであれば望ましい（業界問わず） About the role: The role manages the safety, health and environment of employees involved in projects and new
We are seeking a Legal Entity Controller as a team member who will be involved in local regulatory reporting as well as monthly closing processes. As a Legal Entity Controller - Associate within the Legal Entity Control team,
Blackstone is the world’s largest alternative asset manager. We seek to create positive economic impact and long-term value for our investors, the companies we invest in, and the communities in which we work. We do this
If you are interested in an opportunity where you will have exposures to internal and external clients and specialize in Custody business, this is for you. As a Custody Client Account Services - Associate within Securities Services,
About The Role At ANZ, we’re shaping a world where people and communities thrive, driven by a common goal: to improve the financial wellbeing and sustainability of our customers. Our Institutional bank helps our largest customers
◆部門: HEOR (Health Economic Outcome Research) IQVIAのコアアセットである医療ビッグデータ、及びテクノロジーを駆使した革新的新薬の市販後観察研究、PMS、Health Economics & Outcome Research(HEOR)研究などのエビデンスジェネレーションを推進 ◆業務内容: Real World Evidence(RWES)を使用した複数のプロジェクトのマネジメントや他領域におけるRWESを実務としたプロジェクトチームのリードやチームの参画。 与えられたリソースを基に、プロジェクトの目標を達成/成功させるべく企画からマネジメントまで運営 詳細な情報を記した専門的な文書（例：Statistical Analysis Plans）の発展をリード 高品質な調査と分析を遂行するようチームを先導し、クライアントやステークホルダーに全てのプロジェクトにおいて高い品質と成功をコミット クライアントの新規事業開発における識別と道筋を示し、事業の発展に寄与 ◆論文執筆事例: Japanese Direct-to-Consumer (DTC) genetic testing service An exploratory assessment of the applicability of direct-to-consumer
Let’s be #BrilliantTogether Overview: We are seeking a Research Associate to join our Governance Research Team for Korean Market to deliver excellent corporate governance research the helps investors manage their governance opportunities and risks . Responsibilities: Develop
