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 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
Job Description SummaryThe Senior Statistical Programmer is responsible for all statistical programming aspects of assigned studies or project-level activities. The position is a key contributor with biostatistics in ensuring that pharmaceutical drug-development plans in Novartis are executed
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
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 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 &
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.
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 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
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
