The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, youll be
We will use your ability to integrate/apply knowledge of global & Japanese regulations governing drug development to progressing Regenerons portfolio. This includes preclinical and clinical drug development programs, policies, and procedures. This is an exciting opportunity
This position involves applying a proven understanding of CMC elements and regulatory requirements to support, and provide guidance to Oncology/ Hematology teams in Japan. This position also supports all CMC regulatory filing activities including the preparation
Career Category Regulatory Job Description Job Summary Regulatory CMC Japan Manager is responsible for execution of the Japan-specific product strategies align with the global strategy. This position prepares and submits NDA/CTD/PCA/MCN/consultation dossiers in collaboration with Global
About us BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse
Job Description SummaryAs a CMC development specialist, enhance Japan’s CMC development strategy by offering scientific and technical support to global/local CMC development teams and other departments, while keeping up with the latest technological advancements. [Note] 1:
SUMMARY/POSITION OBJECTIVE: Responsible for achieving Dermatology sales objectives while delivering on Regeneron’s promise to put patients first. Demonstrates superior business acumen, effective management of resources and ability to achieve or surpass corporate goals and sales objectives.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
NP PSL (Product Strategic Liaison) デュピクセントの3つ目の適応症である「鼻茸を伴う慢性副鼻腔炎」のKOL/Product Speaker育成と、本社部門で実施するイベントの企画と実行 Job Description : 1.以下のPSLの役割をリードし、現在・将来の鼻茸を伴う慢性副鼻腔炎（以下CRSｗNP）の適応におけるDUPIXENTの価値をチームとして最大化する強力なスピーカーを育成する。 DUPIXENTのメッセージを全国に広めることで、デュピクセントの価値を最大化し、耳鼻咽喉科治療における生物学的製剤の市場を拡大しつつ、競合に打ち勝つことでファーストラインのポジショニングを確立する。 •KOLマネジメント:波及効果のあるスピーカーの開発育成 •マーケティング戦略の実行:各種イベントの企画・実行（全国講演会、ウェビナー、共催セミナー) •営業活動支援:エリアオピニオンリーダー(AOL)マネジメント支援 •サノフィのプレゼンス向上:耳鼻咽喉科領域主要学会のステークホルダーとの強いrelation構築 •Global発信：日本人KOLを海外へ演者として送り出し、日本から世界へのメッセージ発信に貢献 Selling Point: CRSｗNP治療領域における初のBio製剤登場から、SCS（経口ステロイド剤）でコントロールしていた市場がパラダイムシフトを起こしている 患者さんの主訴である嗅覚障害に速やかにアプローチすることで、日常生活における疾病負荷改善に大きく寄与している 繰り返す再手術でお悩みの患者さんがその苦悩から解放されている 必須経験： •CSA（MR）やMSLとして大学病院や基幹病院を担当し、KOLマネジメントを経験したことのある方 •自身が主幹としてKOLを巻き込んだ新たな組織化や講演会を実施したことのある方 •耳鼻や呼吸器領域（特にCRSｗNP）もしくは、生物学的製剤で専門知識を持つ方 求められるスキル： •リーダーシップと組織マネジメント力 •ビジネススキル（論理的思考、分析力、交渉力、発想力、コミュニケーション、プレゼンテーション、等） •コンピュータ関連スキル：Word、Excel、PowerPoint あれば尚可 •英語：読み書きができる Job Description NP PSL
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative
Are you ready to be a part of Regeneron’s newly created Japan country organization? We are seeking a Manager Commercialization to support the creation and execution of local commercialization activities focused on our sales teams in
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SUMMARY/POSITION OBJECTIVE: Responsible for achieving Immunology sales objectives while delivering on Regeneron’s promise to put patients first. Demonstrates superior business acumen, effective management of resources and ability to achieve or surpass corporate goals and sales objectives.
This is what you will do: The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexion’s product/s across the product/s life cycle. He/she is a peer
■ 職務内容 / Job Description Contribute to maintain sustainably competitive position of AZ in the industry, who can make continued investment on scientific innovation to help patients, by maximizing the value of AZ science through delivering
General Information Job Advert Title: Regulatory Lead, CMC RA International Liaison Location: Nihonbashi, Tokyo Division: Regulatory Affairs Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 Reports to the CMC (Chemistry, Manufacturing and Controls) Regulatory Affairs
General Information Job Advert Title: Director, Clinical Pharmacology Location: Nihonbashi, Tokyo Division: Oncology Development Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 •Have ultimate responsibility and accountability for clinical pharmacology from first-in human through approval,
General Information Job Advert Title: Biologist, Biologics Engineering Location: Tsukuba, Ibaraki Division: Applied Research & Operations Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 Biologics Engineering (BE) is responsible for development of advanced/competitive biologics platforms such as multi-functional
At Cadence, we hire and develop leaders and innovators who want to make an impact on the world of technology. OpenEye, Cadence Molecular Sciences – a division of Cadence Design Systems – is an industry leader
ジェンマブは、革新的で独自性のある抗体治療薬の開発に注力し、患者さんの人生をより豊かにすることを目的としています。 The Role Japan Clinical Pharmacology Lead will serve as the pre-clinical and clinical pharmacology lead on a number of pre-clinical and clinical development programs providing quantitative sciences support and execution of Japan clinical development plans
