[Position Purpose] The Launch Excellence Sr. Manager facilitates the successful launch of Pfizer breakthroughs in Japan, through cross-functional and global-local coordination as early as 3 years prior to launch to ensure that necessary steps (i.e., customer
JOB DESCRIPTION: MAIN PURPOSE OF ROLE • Leads/supervises a team of 2 or more professionals. • First level manager of a work team that could comprise professionals, technical and/or administrative staff. • Typically without budget or
Cochlear is the global market leader in implant hearing solutions. Cochlears mission is to help people hear and be heard. Around the world, more people chose a Cochlear-branded hearing implant system than any other. A Cochlear
Manager, Clinical Operations ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future
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 to
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
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
General Information Job Advert Title: Platform Engineer, Veeva MyInsights Location: Nihonbashi, Tokyo Division: DigitalX Employment Class: Permanent Description 【Purpose & Scope】 As a Platform Engineer of a team of individuals in a specific area of digital
Career CategoryRegulatory Job Description Group Purpose Japan Regulatory Affairs provides leadership, expertise, and execution for the regulatory strategy to obtain and maintain clinical trial and marketing licenses for Amgen molecules in Japan in alignment with local business
Are you passionate about the world of clinical trials? Are you highly motivated by being able to make a difference in improving patients’ lives? The position of Clinical Research Manager provides you the opportunity to work in a
We are looking for a Data Architect Project Leader for an international pharmaceutical firm. You will manage and improve our Real-world Data (RWD) platform for the business. Client Details Our client is a global bio-pharmaceutical company
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
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.
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
■ 職務内容 / Job Description Responsible for leading and managing clinical delivery team of contributing experts to operationally deliver defined clinical studies, or clinical project work package / activities to time, cost and appropriate quality in Japan R&D. Clinical Operations is
Job Description Summary-Defines and drives scientifically sound and business driven project strategy. Reviews, manages, proactively challenges, and controls status of projects operations of the programs and budgets; manages schedules and may prepares status reports. Guides and leads
■募集の背景 Resource Management Group (RMG)では、担当者の異動に伴い、BIツールによるDashbaod開発・運用やレポート作成業務を担当頂ける人員の募集を行います。 ■部署の説明 Resoruce Managment Group (RMG)では、CRAをはじめとした主要Roleのリソース管理、リースや生産性に関連するデータ分析、各種データ集計やレポート生成を行っています。 主なカウンターパートはOperation部門（CRA、CL、PL等）のUnit長やLM、Sr Managment層になります。 ■業務内容 リソースや生産性に関連するデータ集計・管理、およびレポート作成。（SpotfireによるDashboard開発も含む） また、各種データの説明や分析、予測モデルの作成、Operation部門やSr Managementの意思決定支援およびAction Follow。 各種業務で使用するITプラットフォーム（Spotfire等）の運用管理、活用促進。（R&DSのハブとして他部門をサポート） ■応募要件 必須スキル - Word/Excel(関数/マクロ)/Access/PowerPoint - 英語力: 文章の読み書き、メールでのやりとりができるレベル -コミュニケーション/コラボレーションスキル 推奨スキル - BI toolを使用したレポートの開発・分析スキル（TIBCO社Spotfireであれば尚可） - プログラミングスキル（HTML(CSS)/SQL/JS/Iron Python/R言語） - プレゼンテーション/ファシリテーションスキル 求める人物像 - Spotfire(他BI
Job Overview Secure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Will be responsible for multiple CRO line-of-businesses, including clinical trial outsourcing, pharmacovigilance outsourcing, and
■募集の背景 Resource Management Group (RMG)では、R&DS組織の成長に伴う業務の拡大および複雑化を受け、新しい高度なテクノロジーの活用と、分析能力、予測能力の向上と強化のために人員の募集を行いまます。 ■部署の説明 Resoruce Managment Group (RMG)では、CRAをはじめとした主要Roleのリソース管理、リースや生産性に関連するデータ分析、各種データ集計やレポート生成を行っています。 主なカウンターパートはOperation部門（CRA、CL、PL等）のUnit長やLM、Sr Managment層になります。 ■業務内容 リソースや生産性に関連するデータ集計・管理、およびレポート作成。（SpotfireによるDashboard開発も含む） また、各種データの説明や分析、予測モデルの作成、Operation部門やSr Managementの意思決定支援およびAction Follow。 リソースや生産性に関連する社内Initiativeの企画立案・推進、およびSr Managementへの報告。 各種業務で使用するITプラットフォーム（Spotfire、GenAI等）の運用管理、活用促進。（R&DSのハブとして他部門をサポート） ■応募要件 必須スキル - Word/Excel(関数/マクロ)/PowerPoint - 英語力: 文章の読み書き、メールでのやりとり、会話ができるレベル - コミュニケーション/コラボレーションスキル - プレゼンテーション/ファシリテーションスキル - データ集計・分析スキル - プロセス設計・コンサルテーションスキル 推奨スキル - BI
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development
