【職務内容　Job Description】 Data Scientist(DS) is a key player of evidence generation in Medical division of AZ KK. Therefore, DS surely plays following roles. DS directly reports to the director of Data Science, EOR.   1. Advice/co-leading of AZSS To gives advises about the study design, method, endpoints, and analysis from an epidemiological point of view and leads observational/database research with other members in Medical Div. 2. Assessment of study design/target population/data source/data han...

【職務内容 / Job Description】 Project Physician (PP) is a medical expert who is accountable/responsible for the medical science expertise to generate clinical development strategy, design clinical development options, and deliver successful clinical development of responsible products in Japan. PP is working closely with Medical Scientist (MS). His/her accountability/responsibility is mainly project-level, however, he/she is also involved in study-level activities as needed. 1. Project Level 1.1 Desi...

【職務内容　Job Description】 Statistician(STAT) is an key player of coducting observational/database research in Medical division of AZ KK. Therefre, STAT surely plays the following roles. STAT directly reports to the director of Data Science, EOR. 1. Support/advice AZSS from a statistical point of view To gives advises about the study design, method, endpoints, and analysis from an epidemiological point of view and support for observational/database research by providing effective inputs. 2. Assessme...

【職務内容 / Job Description】 Job purpose In line with the Data & Analytics / RWE group objectives, the role holder will Support in delivering the next generation data platform “NexGen” from BI perspective Typically engage with analytics consumers, understanding the business problem, developing the appropriate analytics strategy and ensuring value creation from the insight by the business. Support business insight through the manipulation and analysis of data using statistical, machine learning a...

■ 職務内容 / Job Description Working as a generalist but may have specialist knowledge in a particular Human Resources functional area. Will manage the day-to-day operations within the area and be responsible for implementing policies and managing the HR portal. Is likely to have professional Human Resources qualification. May be a member of a pool of Human Resources professionals working on diverse Human Resources/Business projects.  Advisory work responsibilities including case management, providi...

【Job Description】 The GCO Regional Production Manager – APAC & Japan is a member of the Global Commercial Operations (GCO)’s Global Production Team and reports to the Global Production Director – APAC & Japan. The GCO Regional Production Manager – APAC & Japan is responsible for the development of production services within their respective regional markets. The GCO Regional Production Manager – APAC & Japan is accountable for working with sub Regional/Local Marketing Company Bra...

【職務内容 Job Description】 職務概要 IT戦略／目標に沿って、アストラゼネカ株式会社コマーシャル・ビジネスインテリジェンス／アナリティクス部門について以下の職務を遂行する。 アストラゼネカ株式会社における情報管理システム（Information Management System）を包括的に革新しながらサービスを維持と同時に所属する自グループのメンバーの育成を行う。 データ解析を行うユーザ部門と連携してビジネスの課題を整理し、現状に適したデータ解析戦略を策定するとともに当ビジネス関連インサイトから得られる価値創造を確保する。 役割と責任 データ（社内、社外、構造化、非構造化）のプロファイリング、統合化、トークン化、クリーニング、フィルタリングなどを通じて“解析が可能”な状態に加工し提供する。  ITリーダーや後継者の育成を継続・推進し、ITスタッフへのコーチングやキャリア開発を通じてコア・プロフェッショナルコンピテンシーの開発を行う。 カスタマーグループやステークホルダーと強力な戦略的...

■ 職務内容 / Job Description The Director of Clinical  Quality  Management (DCQM), as a core member of Development Operations Leadership Team (DOLT), is responsible for: ・ providing directions advice on how to use the business processes and quality systems to the both Study Management and Site Management personnel to enable the delivery of projects according to agreed high quality standards and processes toward the goal of inspection-ready clinical studies. ・leading the planning and implementation o...

■職務内容 Execute Evidence generation strategy in responsible therapeutic area under Medical Affairs Director oversight by closely collaborating with MA members, External experts, EOR (Evidence and Observational Research) team and global counterparts so that the studies are properly planned, delivered and published to address Key Research Questions and unmet medical needs that support Business strategy. Deliver high-quality scientific and strategic evidence through AZSS and ESR, with Scientific publ...

■職務内容 【ミッション】 ・優れた製品戦略の立案と実行を通して製品およびポートフォリオのベネフィットを一人でも多くの患者さんに届け、AZのサイエンスの価値を最大化することで、 患者さんのためにサイエンスに再投資し続けられる製薬企業として競合優位性を維持し続けることに貢献する 【業務の範囲】 ・市場環境、顧客、製品およびポートフォリオを深く理解し、ブランドチーム、関係部門と協力しながらビジネス課題を特定・構造化・分析し、課題を解決するための製品戦略（上市プラン）を立案する ・製品戦略に基づく実行プランの一部を立案・実行・評価まで責任を持って実施する ・市場環境の正確な理解、戦略立案のための仮説の検証、打ち手の評価を一次・二次調査により明確にし戦略の検証・改善を行う ・戦略の立案・実行に際して社内外のステークホルダへ提案し、承認・サポートを獲得する ・営業部門を始めとする他部門とのコミュニケーション、KEEのマネジメントを円滑に行い、戦略の実行を徹底する ・GPPSを始めとするグローバルチームと協力しながら日本に留まらない製品価値の最大化をサポートする ■応募...

AstraZeneca is a global, innovation-driven biopharmaceutical business with a primary focus on the discovery, development and commercialisation of prescription medicines. Our purpose as a company is to push the boundaries of science to deliver life-changing medicines and greater efficiency & innovation in healthcare. AstraZeneca IT’s Cloud Platforms and Digital Solutions (CPDS) team delivers public and private Cloud services to internal customers. These services range from Cloud Advisory, Aut...

【Job Description】 The Project Leader is a cross-functional project leader of relevant Project Team to build and execute project strategy (ies) of a development product(s), including NME project(s) and/or LCM project(s) which require clinical trial(s) in Japan. The Project Leader provides the leadership to the project team(s) to build high performing team(s) for maximizing the value of product(s) in Japan. The Project Leader is accountable for the responsible project strategy (ies), and is a sing...

【職務内容 / Job Description】 To deliver clinical studies in Japan Manage a cross functional team of clinical experts to operationally deliver defined clinical studies or assigned clinical project activities to time, cost and appropriate quality including documentations.   Provide input into study start up activities (e.g. study feasibility, study specifications, vendor/partner contracts, authoring of clinical study protocols and budgeting including authorization and governance of payment). Oversee t...

【Job Description】 Japan Associate Director Clinical Development (J-ADCD) is accountable/responsible for leading the project planning for clinical operation in Japan R&D. The span of activities is broad covering clinical activities in both early and late drug development, registration/submission and post registration product maintenance phases and will include local and global working. The J-ADCD is responsible for planning, oversight on related studies and mediator among Japan study team, pr...

■職務内容 Data Engineer is an expert role of server management in Medical division of AZ K.K. Therefore, Data Engineer plays a following role in a timely manner. Data Engineer directly reports to the director of Data Science, EOR.  Management of Japan Data server • Develop appropriate processes for utilizing data server • Assess applications for Amazon Web Service(AWS), especially statistical & new technology • Install/upgrade softwares in server • Assess server performance and correspond to its...

【職務内容 / Job Description】 Project Manager is responsible for leading and project managing cross-functional Japan Project Team (JPT) to ensure alignment of operational delivery with project strategy, enable and drive project delivery and informed decision making, and ensure that each project is established and managed in a way that best represents best practice for project management within AZ.  The spectrum of this role varies based on factors such as the scope of tasks and status of the projects...

■ 職務内容 / Job Description Clinical Scientist (CS) is accountable/responsible for the medical science expertiseto generateclinical development strategy, design clinical development options, and deliver successful clinical development of responsible products in Japan.   His/Her accountability/responsibility is mainly project-level, however, he/she is partially involvedin study-levelactivities, too, in order to achieve project-level delivery. ■ 応募資格（経験、資格等）/ Qualification (Experience &...

■ 職務内容 / Job Description Japan Regulatory Lead (JRL) is responsible for planning and execution of Japan regulatory strategy of the assigned products/projects by Providing strategic regulatory expertise for optimum market access of the products in Japan as a member of Japan project team and Global Regulatory Strategy Team(GRST) Leading communication of the global regulatory strategy and its implication to Japan so that the context of regulatory input are properly understood by the governance bodi...

■ 職務内容 / Job Description Responsible for the authoring of clinical-regulatory documents and submission packages that communicate the evidence base of product knowledge in a credible, consistent and compliant way. ■ 応募資格（経験、資格等）/ Qualification (Experience & Skill etc) 【経験 / Experience】 ＜必須 / Mandatory＞ Experience in medical communications gained through working in the pharmaceuticals industry or a medical communications agency A comprehensive knowledge of the drug ...

【職務内容 / Job Description】 Produce SAS programs and documents (e.g. specifications and mock shell) to deliver the tables, listings, figures (TLFs), Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) based on agreement with user representative.  Produce accordingly define.xml, Study Data Reviewer's Guide (SDRG), Analysis Data Reviewer's Guide (ADRG) and Analysis Results Metadata (ARM). Lead, contribute and/or support from the aspects of the Programming field toward submission...