Basic Purpose of Job Manage case processing activities for Nippon Boehringer Ingelheim’s investigational and marketed products including case submission to Global Patient Safety and Pharmacovigilance (PSPV) and PMDA according to Boehringer Ingelheim (BI)’s internal procedure and local regulation.
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last
Drug Safety Associate - Tokyo Osaka - Office Hybrid ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration,
Japan Study Managerは、日本国内において治験の管理・監督を担い、CROや治験実施医療機関と連携しながら、治験参加者の安全と福祉、治験の品質を確保し、治験の計画通りの実施をリードします。グローバル・ローカル双方と連携し、課題解決や進捗管理も担当します。 JOB SUMMARY & RESPONSIBILITIES Responsible for in country study/site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices
Overview :We are seeking a Sales Specialist for the worlds most widely used chromatography data management system.:You will work as part of a team, collaborating with sales and marketing staff.:Remote work is possible if needed. Responsibilities
Overview 【組織構成】 少人数グループでフラットな組織体制になっています。20代～40代の、幅広い年齢層の社員が活躍しています。 社員の多くがが中途入社で、様々な経歴者が働きやすいように、風通しの良い環境を提供しております。 また年令や職位に関係なく互いをさんづけ呼び合うフランクな組織体です。 Wyatt光散乱装置およびAura装置に関する営業、営業開発、およびカスタマーサクセスに関する取り組みを支援していただきます。 Responsibilities 【業務内容】 • 担当アカウント／担当地域において、現地営業チームと連携し、オンサイトセミナー、技術コンサルティング、およびアプリケーションの実用性テスト（デモンストレーション）を実施することで、新たな販売機会を積極的に開拓する。• 初期段階の商談を、技術的な合意に至るまで管理する。• 販売プロセスにおける技術的なアプリケーションサポートを習得し、トレーニング、顧客成功支援、高度なトラブルシューティング、データ分析を含む販売後の訪問業務を行う。• 既存顧客に対し、継続的な販売後のサポートとして、高度な製品トレーニングとアプリケーションサポートを提供し、リピート販売を促進する。• バイオ医薬品、特殊化学品、学術市場におけるプロセス最適化および開発の権威として認められるよう、アプリケーションに関する深い知識と専門性を養う。• 業界セミナー、カンファレンス、シンポジウムにおいて、主要なアプリケーションに関する技術資料を作成し、発表する。• バイオ医薬品および遺伝子治療市場に高い価値を提供するアプリケーションソリューションを特定し、開発する。 Qualifications 【求める人材】 • 化学、生化学、または同等の分野の博士号。あるいは、修士号または学士号を取得し、5年以上の関連実務経験を有すること。• HPLCおよび光散乱分析装置の実務経験5年以上• 高分子およびタンパク質分析技術に関する知識• 優れたコミュニケーション能力および対人スキル、基本的なデジタルリテラシー• 優れた文章力および口頭でのコミュニケーション能力、ならびに基本的な実験技術、装置、ソフトウェアに関する深い知識。• 優れた組織力、自発性、細部への注意力、およびコミュニケーション能力が必須です。 Company Description Waters Corporation (NYSE:WAT) is a global leader in life
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials
Job Description Position Overview The Specialist, Quality Systems & Compliance is an individual contributor who supports key GQP Quality Assurance activities on behalf of the Marketing Authorization Holder (MAH). The role plans and executes assigned quality
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Overview The EHS (Environment, Health & Safety) Manager – Japan is responsible for establishing, implementing, and managing EHS programs in compliance with Japanese regulatory requirements and corporate standards. This role supports all Waters sites (except manufacturing) across
Overview As Waters accelerates its cloud transformation and strengthens its industry leading informatics portfolio, a dedicated leader is needed to drive execution, revenue growth, and customer engagement in the Americas. This leader will be responsible for
MAIN REPONSIBILITIES / DUTIES JOB POSITION PURPOSE The MAS role family comprises a variety of medical scientific specialties, such as BU Medical and field based Medical. Be the Pfizer Japan medical scientific point of contact for
職務内容 スタディ・マネジャーは、日本国内において治験の管理・監督を担い、CROや治験実施医療機関と連携しながら、治験参加者の安全と福祉、治験の品質を確保し、治験の計画通りの実施をリードします。グローバル・ローカル双方と連携し、課題解決や進捗管理も担当します。 JOB SUMMARY & RESPONSIBILITIES Responsible for in country study/site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP),
1. Objectives Responsible for clinical development of the assigned project in Japan under the supervision of the Japan Development Leader (JDL), who assumes responsibility for development of all projects in Japan in the respective therapeutic/disease area
MAIN REPONSIBILITIES / DUTIES JOB POSITION PURPOSE The MAS role family comprises a variety of medical scientific specialties, such as BU Medical and field based Medical. Be the Pfizer Japan medical scientific point of contact for
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Job Description SummaryJoin Novartis and play a critical role in shaping a safe, sustainable, and compliant work environment across Japan. As the Site HSE Manager for Commercial Operations, you will lead impactful Health, Safety, and Environment initiatives
Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution
Job title: Clinical Operations Study Country Lead (COSCL) Location: Tokyo, Japan About the job Our Team: We are seeking a highly motivated and experienced Clinical Operations Study Country Lead to support local clinical trial operations. The
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last