（職務内容） Provide input to or assess Medical activities, especially eveidence generartion activities as medical/scientific/clinical reseach expert in the therapeutic area he/she is responsible for, and maximize the value of products in the therapeutic area through AZ Medical activities. Bring clarity to the clinical positioning of the products and the gap to fulfil for desired clinical positionng in the therapeutic area by deeply understanding external experts’ comments, eliciting the...

【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部門で以下の職務を遂行する。 グローバルとローカルで推進するプロジェクトを牽引し、目的とするプロジェクトの利益を達成する。 稼働状態となった営業支援システムを、ユーザー部門と合意をしたサービスレベルで健全に運営し続け、運用改善を行う。 ビジネスユーザー部門からITニーズを取りまとめ、ビジネス効果を最大限に引き出すIT提案を行う。 ＜役割と責任＞  IT資源の効果的な活用と持続可能な運用を通じてビジネスの価値を最大化する。 ビジネス要件とAZのエンタープライズアーキテクチャーが連携したITソリューションをAZ標準ITインフラストラクチャー下でデザインする。 ビジネスケースの作成。並びにビジネス戦略の支援、改善、変革のためのビジネス要件や情報ニーズの分析を行う。 ステークホルダーやレビュー委員会が効果的な意思決定を行えるように、プロジェクト予算、予測、タスク、日程、リスク、変更管理、進捗管理などの管理と調整...

(職務内容） Evidence Delivery Operation Specialist (EDOS) is the Operational Project Management role to drive effective delivery of AstraZeneca Sponsored Studies(AZSSs)/Externally Sponsored Researches(ESRs) to time, cost, quality and expected values Strategic Evidence Planning • EDOS contributes the cross functional strategic evidence planning and Business Planning Process so that the Evidence Generation costs are properly forecasted, phased and managed Study Delivery Operations • Lead all ope...

■職務内容 ・泌尿器腫瘍領域のScientific expertとして顧客の1次対応窓口として関係構築をおこない、メディカル活動をけん引する。 本領域における製品を担当し、新製品の上市前準備、上市後の製品価値の最大化に向け疾患・製品啓発のための活動をおこなう。 主な仕事内容として、 ・外部顧客（Key External Expert, KEE）との関係構築 ・最新の医学・医科学情報をもとにKEEとディスカッションをおこない、担当領域におけるUnmet medical needs・インサイトの収集と分析 ・担当領域における、エビデンスに基づいた疾患・病態・製品価値に関する説明 ・上市前製品（未承認薬、承認薬の用法・用量適応外を含む）の質問に対し、科学的中立な立場からエビデンスに基づいたリアクティブな情報提供 ・科学的に中立な立場で実施するScientific Exchange Meeting （SEM）の企画・運営 ・メディカルが主催するイベントの実施支援（Advisory board me...

【職務内容】 ■乳がん・卵巣がん・前立腺がん領域 MR 乳がん・卵巣がん・前立腺がん領域の医療施設医師・薬剤師に対する医薬品の情報提供活動および適正使用の推進 【応募資格(経験、資格等)】 ■経験 Experience 必須 Mandatory 基幹病院担当MR経験3年以上 歓迎 Nice to have オンコロジー領域製品の経験 大学病院担当経験 ■資格 License 必須 Mandatory MR認定試験合格 普通自動車免許 ※英語力不問 ■その他 Others 必須 Mandatory 全国勤務可能 【勤務地】 全国各拠点 Date Posted 24-12月-2019 Closing Date 16-2月-2020 AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspect...

【職務内容　Job Description】 ■オンコロジービジネス領域において、ブランドプランの理解度を上げ、アクションの推進と課題の抽出、仮説検証・対策案を提示すとることで、成果に貢献する ＜Strategy&Planning＞ ・各ブランドの全国の営業計画策定のプロセスにおいて、マーケティングとともに戦略・戦術の進捗と、その販売実績に及ぼす効果を客観的に評価できる実務プロセス（KPI）を確立する​ ・領域・ブランドをまたがり、各プロモーションプランにおいて、領域MRの活動のfeasibilityを調整するとともに成果の最大化となるプラン策定に貢献する ＜Execution＞ ・SFEとともに各ブランドの全国の営業計画をもとに作成されるエリアプランのガイダンスの作成、及び最終化までのプロセスを管理し、プランの一貫性を担保する ・全国、営業部並びに課毎の実績の・KPI進捗状況をから、仮説を立て、課題を抽出し、BUH/SID（SID KPI会議時）, TADÿ...

《職務内容》 Analyses compensation and benefits data to develop recommendations which inform decision-making.  Carries out pay and benefit benchmarking in order to monitor the cost-effectiveness and competitiveness of the reward package. Supports cyclical processes within the performance, compensation and benefits areas and contributes to system and policy reviews. • Carries out analysis of compensation and benefits data within the framework of the Global Reward Strategy. • Participating in reviews an...

【職務内容 / Job Description】 Acting as the main line of communication between the sponsor and the investigator. Communicate with Japan Study Leader and third party vendors as needed. Conduct site selection activities for verifying adequate qualifications. Manage and monitor the responsible sites and ensure their quality appropriately, agreed cost spent and on a timely basis. Ensure input the latest site related information in IMPACT at appropriate timing. Participate in-house and/or external clinica...

Job Purpose The BI and DWH System Architect and Data Architect role will typically work within a team to fulfil IT Architecture tasks under supervision of a more senior member of the function. This role is responsible for enhancing and accelerating projects while ensuring the logical and physical architecture for a project aligns with the standards and reference architectures defined by enterprise architecture. The role will assist more senior team members with delivering the architectural desig...

■職務内容 Provide input to or assess Medical activities, especially eveidence generartion activities as medical/scientific/clinicalreseach expert in the therapeutic area he/she is responsible for, and maximize the value of products in the therapeuticarea through AZ Medical activities.Bring clarity to the clinical positioning of the products and the gap to fulfil for desired clinical positionng in the therapeuticarea by deeply understanding external experts’ comments, eliciting their views, and makin...

■職務内容 Japan EOR Medical Evidence Science leader is an expert role in clinical research to provide scientific expertise in Medical Evidence generation so that key research questions are sufficiently addressed, and all programs are planned and delivered in a way that represent cutting-edge science, methodologies, technologies, process and solutions in the industry. MESL will report to director of Data Science director, EOR and have no line management responsibilities.Strategic Evidence Planning • ...

■職務内容 Japan EOR Evidence Delivery Leader(EDL) is a project leadership role in delivering AZ sponsored scientific studies and medical evidence generation to support AZ business and value claims, in line with strategy, governance processes and standard operation procedures. Business Planning & Control • EDL supports Therapeutic Area Medical Affairs(TAMA) Team in organizing the cross functional strategic evidence planning workshops for quality evidence plans • EDL supports Business Planning Pro...

■職務内容 呼吸器疾患/アレルギー領域のScientific expertとして顧客の1次対応窓口として関係構築をおこない、メディカル活動をけん引する。 本領域における製品を担当し、新製品の上市前準備、上市後の製品価値の最大化に向け疾患・製品啓発のための活動をおこなう。 主な仕事内容として、 ・外部顧客（Key External Expert, KEE）との関係構築 ・最新の医学・医科学情報をもとにKEEとディスカッションをおこない、担当領域におけるUnmet medical needs・インサイトの収集と分析 ・担当領域における、エビデンスに基づいた疾患・病態・製品価値に関する説明 ・上市前製品（未承認薬、承認薬の用法・用量適応外を含む）の質問に対し、科学的中立な立場からエビデンスに基づいたリアクティブな情報提供 ・科学的に中立な立場で実施するScientific Exchange Meeting （SEM）の企画・運営 ・メディカルが主催するイベントの実施支援（Advisary boa...

■職務内容 【Description】  A leadership role responsible for developing strong confifence building strategy and ensuring all field medical strategic plan aligned with TA strategy. Proactively demonstrate the AZ Values.  • Headquarters-based position responsible for leading TA MSL team in establishing scientific leadership of AstraZeneca. • Will be expected to develop and implement confidence building strategy and plan of responsible TA through Medical activities with building strong engagement with ex...

We are building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we are opening up new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Talent Acquisition at AstraZeneca has transformed.We have built a world class function by being more proactive with our recruitment approach and developing long term pipelines of talent. We are passionate about delivering a truly differentiated candidate experience and a...

【職務内容 / Job Description】 Risk Management & Safety Scientists are responsible for setting product safety specifications and for delivery of local Risk Management Plan (RMP), and J-PI (safety parts) to optimize market access from patient safety perspective in Japan. RMP Team Leads manage setting the project safety strategy in view of ‘Benefit and Risk valance’ of each product by planning the appropriate risk minimization activities and pharmacovigilance plan including regulatory mandatory phar...

【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】 Medical Scientist (MS) 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.  His/Her ccountability/responsibility is mainly project-level, however, he/she is partially involved in study-level activities, too, in order to achieve project-level delivery. Accountability/Responsibility 1 Project Level 1.1 Design...

【職務内容 / Job Description】 Safety Operation group staff is responsible for collecting, evaluating, and submitting safety information to the relevant parties (e.g., PMDA, AZ global Patient Safety, licensing partners)  in compliance  with regulatory authority requirements, internal procedural documents and safety agreements by collaborating with outsourced vendor. Accountabilities/Responsibilities: Deliver training to the members who are responsible for collecting safety information (e.g., sales rep...

【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 governanc...