Job Purpose メディカルアドバイザーとして、医療・科学的観点から患者アウトカムの向上に貢献する Key accountabilities/Responsibilities メディカル戦略の立案に医療・科学的観点から貢献し、それに基づいたプロジェクトを遂行する メディカル戦略の立案において医療・科学的観点からMedical Leadにinputする 社内ステークホルダーに対して、医療・科学的観点からサポートする Medical活動やその他のNon-Promotional活動、Promotional活動が社内および国内外のガイドラインを遵守しながら、医学的・科学的に正しく遂行されることを担保する Key opinion leaderやKey authoritiesと科学的なディスカッションができ、良好なコミュニケーションをとる GSKの製品に対して、メディカルとして適切な情報提供をする 社外ステークホルダーとメディカル戦略を最大化するためのコミュニケーションをとる Job purpose Contribute to patient’s outcome from medical and scientific perspective. Key Accountabilities/Responsibilities: Contribute to development of medical strategy with
Head of Japanese Accounting & Finance About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases
Are you interested in a regulatory affairs role that allows you to mitigate risk and accelerate compliance across the business? If so, this Regulatory Compliance Manager could be an ideal opportunity to explore. As a Regulatory
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.
* Responsible for preclinical of J-NDA * Contribute to the successful development of early projects and development pipelines from a toxicology and DMPK expert perspective 企業情報 * European multinational pharmaceutical and biotechnology company * Wide range
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 of
At Regeneron, our medical affairs physicians and scientists are at the forefront of innovation, playing a crucial role in our global development organization. As a key liaison between Regeneron and the scientific and healthcare community, you
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Be in charge of finance reporting between HQ (Japan) and oversea subsidiaries for a historic Japanese pharmaceuticals company in an international working environment | Career path, international mobility opportunities, WFH and flex time available. Client Details
* Lead market and sales analysis, forecasting, and competitive intelligence for a major pharma company. Collaborate with cross-functional teams to drive strategic insights that maximize brand performance. Client Details * US bio-pharmaceutical company, with rich development
As a Manager in Market Access & Marketing, you will oversee insurance applications, regulatory submissions, and launch strategies for advanced cancer diagnostics. You will also lead a marketing team and drive commercial success for the Oncomine
As a Commercial Project Manager, you will oversee the full lifecycle of oncology diagnostic programs, driving them from concept through commercialization. You will lead cross-functional coordination with internal teams and external clients to ensure timely product delivery
* ユーザーの技術的課題や実験デザインに関する問題を解決 * 顧客との関係構築とフィードバックを活かして製品の改善に貢献 企業情報 * 次世代のゲノム解析技術を提供し、医療、研究、農業分野における革新を牽引するグローバル企業 * 製品：NGS、マイクロアレイシステム、ライブラリ調製キット、Oncology Precision Testing製品等 職務内容 * 新規インストールを調整し、機器の検証や顧客トレーニングを実施 * ユーザーの技術的課題や実験デザインに関する問題を解決 * 技術プレゼンテーションやデモンストレーションを通じて製品使用を促進 * 顧客との関係構築とフィードバックを活かして製品の改善に貢献 理想の人材 * NGS技術の使用経験、知見 * 修士もしくは以上のご学歴 * customer-facingのご経験（FAS・技術サポート・営業）等の経験は尚可 条件・待遇 * 他の学者の研究活動をサポートし、large-scaleに医学の発展を影響する機会 * ゲノミクス領域にて知名度の高い企業にて長期的なキャリアを築く * グローバルなビジネスカルチャー * 在宅の頻度が多いフレキシブルな働き方 Page
Take lead in RA activities to obtain product approval. Ensure effective submission requirements as well proper timelines of new/existing regulatory projects. Client Details * One of the top global pharmaceutical companies in the industry * Specializing
＜Associate Brand Manager＞ ■ 職務内容 / Job Description ■ミッション 優れた製品を一人でも多くの患者さんに届け、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 ・イベント（TV講演会等）の立案・交渉・実行・レビューの実施 ・プロモーション資材（パンフレット・説明会スライド・MR君*コンテンツ等）の立案・作成・実行・レビューの実施 (*MR君: 医薬品、疾病、治療等医療に関する情報を提供するツール) ・営業部門への企画・戦略等のコミュニケーション ・KOL (Key Opinion Leader) のマネジメントの遂行 ・マーケティング・営業活動のKPI (Key Performance Indicator) モニタリングや営業ツール等の社内システムを他部門（IT等）と協業し構築 ・メディカル本部・Commercial Excellence本部(営業やマーケティングの支援部門)・Pharmacovigilance部など他部門との活動の共有、及び、調整 ・市場環境、顧客、製品およびポートフォリオを深く理解し、Brand Managerの製品戦略立案のサポート ■ 応募資格（経験、資格等）/ Qualification (Experience & Skill
* Enhance the performance of a major pharma companys sales force by optimizing brand communication and improving resource allocation. Use analytics and CRM tools to drive strategic initiatives and maximize impact. Client Details * US bio-pharmaceutical
Take lead in RA activities to obtain product approval. Ensure effective submission requirements as well proper timelines of new/existing regulatory projects. Client Details * One of the top global pharmaceutical companies in the industry * Specializing
Be part of one of the top global pharmaceutical businesses in the industry. Take lead in GCP audits for the company to ensure regulatory compliance. Client Details * One of the top global pharmaceutical companies in
Be the expert in company QMS to ensure in GxP requirements (GQP/GMP) areas. Support in the Hinseki to ensure effective quality compliance based on local regulations. Client Details * Global leading biopharma business with cutting edge
