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 and
Key Account Manager – Oncology Japan At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming
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,
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
Job Opportunity: Lead, Japan Clinical Operation Program (JPD, Lead) Location: Osaka or Tokyo Job Reference: R-202457 Date Posted: 06/16/2024 General Description The Lead, Japan Clinical Operation Program (JPD, Lead) is responsible for leading the project planning for clinical operations
Job Opportunity: Project Manager, Laboratory - Japan, Tokyo (Hybrid: Office/Remote) About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. Proudly fostering an inclusive environment that drives innovation and excellence, the organization welcomes
Job Opportunity: District Manager (DM) Overview Our client is looking for a District Manager (DM) who will co-create and embed a high-performance team culture aligned with the companys vision, values, and strategic direction. You will manage
募集職種: プロジェクトマネージャー（ラボ） - 日本、東京（ハイブリッド: オフィス/リモート） 会社概要 弊社クライアントは、世界有数のヘルスケアインテリジェンスおよび臨床研究機関です。革新と卓越を推進するインクルーシブな環境を育むことに誇りを持ち、臨床開発の未来を形作る使命に一緒に参加することを歓迎します。 職務内容 現在、東京にある多様でダイナミックなチームに加わるプロジェクトマネージャー（ラボ）を募集しています。プロジェクトマネージャー（ラボ）として、ラボの運営およびプロジェクトを監督し、ラボプロセスおよび成果物のタイムリーかつ正確な実行を確保する重要な役割を果たします。ラボのワークフローの最適化および戦略的監督を通じて、革新的な治療法の進展に貢献します。 主な業務内容 * クライアント満足度: 日々の研究管理を含むサービスに関するすべての事項でスポンサーの主な連絡先として行動し、クライアントの満足度を確保する。 * 代表: スポンサー会議に出席し、組織を代表する。 * 研究管理: Good Clinical Practiceに従って10〜15の研究を管理する。 * コミュニケーション: 研究の進捗を責任を持って専門的に報告し、スポンサーに定期的な管理レポートを提供する。 * サポート: スポンサーの担当者にICOLABサポートを提供する。 求める人材 * 学歴: 生命科学またはヘルスケアなどの関連分野の学士号を保有。 * 経験: ラボまたは臨床研究環境でのプロジェクトマネジメントの経験があること。 * スキル: * 優れたコミュニケーションおよび対人スキルを持ち、スポンサー会議で会社を代表できる能力。 *
JOB description To keep up and improve the local supply processes in Japan including roles and responsibilities of involved local and global functions as well as the SOP system which should be in line with global
Job description: 1. To keep up and improve the local supply processes in Japan including roles and responsibilities of involved local and global functions as well as the SOP system which should be in line with
Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines
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 part of
Job Description SummaryAccountable for the oversight and coordination of program and study level (re-)feasibility assessments in the country, in collaboration with program and/or trial feasibility teams, in compliance with Novartis processes, GCP, ICH and regulatory requirements.
Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core
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.
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.
■ 職務内容 / Job Description Responsible to coordinate the Clinical Data Management (CDM) deliverables on assigned clinical projects and may be an expert on CDM processes, standards and technologies, such as EDC and other tools (PV提供用 安全性差分レポートツール, etc.).
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
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.
Career Category Clinical Job Description Purpose: Provide clinical site contracting services to clinical study teams to support study start up and conduct activities Context: Amgen K.K. office Reports to CTOM (Clinical Trial Oversight Manager) Responsibilities Manage end to end process
