JOB DESCRIPTION: General Summary: Provides project management and leadership to plan, prepare and execute high-quality large scale and/or complex clinical program(s). Leads the clinical project team members toward the completion of deliverables in a timely fashion
Are you passionate about driving strategic initiatives and programs in the field of Real-World Evidence (RWE)? Would you like to work in a highly scientific, professional, and global environment? If so, we have an exciting opportunity
Job Description 臨床試験の生物統計担当者として、国内外の臨床開発チームとコミュニケーションを取りながら、主に次の業務を行う 【業務内容】 ・開発戦略および試験デザインの検討 ・統計解析計画の作成 ・試験データの統計解析および結果の解釈 ・統括報告書およびCTDの作成 ・規制当局との対応 【必要条件】 ・生物統計の担当者として３年以上の経験 ・統計または、関連領域の研究による修士の学位 ・統計学の知識の習得を積極的に行っている ・SASのプログラミング経験がある ・英会話力（TOEIC 730点以上もしくは同程度） ・国内の臨床開発チームとのコミュニケーション力がある ・生物統計の実務担当者として積極的に手を動かし、業務を行う意思のある方 【望ましい条件】 オンコロジー領域担当の経験がある Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck
Job Description Summary To manage business and operational activities of local regulatory writing (RW) to ensure timely production of high quality clinical documentation. To ensure compliance with global RW strategy and implementation of technical activities &
General Information Job Advert Title: Lead HEOR Location: Nihonbashi, Tokyo Division: Medical Affairs Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 As Lead HEOR, you will be an integral part of the Medical Affairs Japan
DESCRIPTION OF JOB RESPONSIBILITIES Primary Function Source, interpret, generate and disseminate high-quality evidence and insights from Real World Data (RWD) timely to guide and support business decisions across all therapeutic areas. Act as an expert in
Job Description Summary To serve as a liaison to the medical/ scientific community and responsible for establishing, developing and partnering with Health Care Providers/ Professionals (HCPs) and HCS. To implement clinical and educational strategies in collaboration
Position Purpose - Design, Analyze, and Interpret Clinical Trials/Post Marketing Surveillance (PMS) in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide scientifically rigorous statistical expertise and contributions by working effectively within the
* Design, Analyze, and Interpret Clinical Trials/Post Marketing Surveillance (PMS) in compliance with relevant regulatory requirements 企業情報 Top Global Pharma in the specialized field 職務内容 * Provide scientifically rigorous statistical input into study design, statistical analysis
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.
