At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring
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
＊Business-level Japanese (speaking, writing & reading) is required for this position. ＊応募の際、次の書類をアップロードしてください（新規のかたはページ右下の応募するよりアカウントご作成いただけます）： 履歴書、職務履歴書、英文レジュメ |仕事内容 ・ネスレIT基盤の上、データ分析やAIアプリケーションのアーキテクチャを設計し、技術的な要素やデータフローを定義する ・GlobalやZoneのデータ分析やAIチームと連携し、Marketにおいて、適切な技術、ツール、フレームワークを評価・選択する ・具体的にTrade Spend Optimization、Market Spend Optimizationのようなアプリケーションを開発、運用保守する ・データソース、システム、プラットフォームの統合を監督し、データフローを円滑にする ・データ分析やAIアプリケーションの拡張性とパフォーマンスを確保し、効率を最適化する ・セキュリティ対策を実施し、コンプライアンス基準と規制に準拠する ・ビジネスオーナーやベンダー含むステークホルダーと協力し、要件を理解し、技術的なソリューションを伝える ・デザイン文書や技術仕様を含むドキュメントを作成・維持する ・先端技術やユースケースに注視し、データ分析やAIアプリケーションのパフォーマンスと効果を継続的に監視し、改善する （変更の範囲） 会社の定める業務 【部署紹介】 B2B B2Cシステム及び関連デジタルサービスの構築・保守・運用を行っています。 【部署構成】 総数30名（男性18名 / 女性12名）
Company Description Believe is one of the world’s leading digital music companies. Believe’s mission is to develop local artists and labels in the digital ecosystem by providing them the solutions they need to grow their audience
Job Overview Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies
部門：安全性部門 Product Specialist メインの業務内容： 顧客から新規案件についてRFP ( Request for Proposal ) を受領したら、見積書と提案書を作成する役割。 その他状況により、PM的な役割も担っていただく。 必須経験：PV経験5年以上 、英語スキル （英語面接が最終面接） Job Overview Accountable for management and service delivery excellence of a range of large sized regional and global projects as assigned, covering
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
Basic purpose of the job* The Head of Development Regulatory Affairs 1 or 2 has responsibility to develop and implement regulatory strategy for the assigned therapeutic areas (TAs) and exercises activities which include: Guide subordinates on
Role Description: Inside Sales Associate - Japan Role Purpose Wasabi’s Inside Sales Associate is a crucial part of Japan Sales Team. You will be a hunter, calling on new prospects to help them move to Wasabi’s
Basic purpose of the job Independently writes and manages clinical documents, such as clinical trial reports, Investigation Brochures, Protocols and briefing documents, in both local and global cross-functional project- and study teams, as well as local clinical
ベーリンガーインゲルハイム製薬株式会社 勤務地：大崎オフィス（国内出張あり） ＊日本語の応募書類に加え、できれば英語CVもご送付をいただけますと幸いです。 1. CMOにて発生する各種変更(原薬・副原料・機器等)に対して、CMOからのQualification計画を製剤技術の観点からReviewし、実行する。 （工業化検討・PQ/PV計画書/報告書Review, 必要に応じて現場立会い） 同様にCMOと協議し、Process堅牢化・改善を進める。 2. 新製品の中で、ドイツからの完成品輸入品、国内CMO包装品について、立上げ準備を行う。 技術的な立場から日本国内での新製品立ち上げProjectに参画し、ドイツ・国内CMOと協力しながら準備を進める。 3. CMOにて発生する各種変更に伴う、承認書への記載内容変更案のReview 新製品の薬事申請書類のReview Basic purpose of the job* •Prepare for the initial production for the launch of new products (FG import or Japanese CMO packaging)
Basic purpose of the job HEOR Manager or Senior Staff will be responsible for and lead the development and implementation of the evidence generation strategy to maximize Boehringer Ingelheim asset value and optimize access to medicines
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen
Basic purpose of the job The manager of RRL JP provides strong leadership to develop and implement regulatory strategy for the assigned products/projects as RRL JP, and exercises activities which include: An integral member of the
Basic purpose of the job Insight Generation Manager is responsible for supporting therapeutic area teams with medical insight management. The role involves ensuring proper recording of scientific insights, resolving technical issues with insight capturing platforms, and analyzing
Publication Strategy Manager パブリケーションストラテジーマネージャー Basic purpose of this job: 各疾患領域の戦略に沿った、研究データの適切適時なパブリケーション（論文公表・学会発表）を推進する役割です。 To define and execute the local publication plans in a strategic and compliant manner, considering the overarching HPBU and brand specific strategy and ensuring: - regular
JOB SUMMARY: Briefly state the objective of this position. JCS supports Japan Clinical Lead (JCL) activities in the development and execution of clinical development strategy for target indication(s) in assigned compound(s) to obtain regulatory approval in
Job Description The position takes a responsibility for medical contents in all clinical development programs in assigned therapeutic areas (such as dementia, movement disorders, neuromuscular, and MS/Immunology etc.) in Japan. The individual functions as a scientific
Job Description SummarySite relationship management role to ensure sustainable trial start-up at Site. The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within
