• 東京23区
    正社員
    日系企業

    診療放射線技師資格保有者を求めています。

    先行他社がいる業界ではなく、自らが進む道を切り開いていく面白さがあります。

    • 診療放射線技師資格保有者を求めています。

    • 先行他社がいる業界ではなく、自らが進む道を切り開いていく面白さがあります。

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  • 東京23区
    派遣社員
    外資系企業

    治験に関する文書の作成補助およびQC業務をしていただきます



    • 治験アシスタントをしたことある方必見！注目のヘルスケア企業でお仕事！

    • 日比谷の有名ビルに入ってるきれいなオフィスでお仕事

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  • 日本
    正社員
    外資系企業
    • Produce an manage SAS programs and related documents to ensure all trial and project deliverables are met within the allocate timeline

    • Utilize Statistical Programming Expertise to Expedite Clinical Trials

    • Contribute to Approval of Innovative Medicines

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  • 日本
    正社員
    外資系企業
    • Serve as a program or study-level programmer in a defined development program
    • Support the programming and analysis of clinical studies within current and future development compounds or across multiple compounds/areas of research

    • Work for Science Focused European Biopharma

    • Lead Statsitical Programming Activities in Global Clinical Trials

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  • 日本
    正社員
    外資系企業


    • Responsible for the operational management and oversight of clinical trials within a clinical development program


    • Manage the successful execution of clinical trials from the protocol concept through the clinical study report, ensuring completion of study deliverables

    • Industry Leading Biopharma Company in the Development of Anti-Cancer Therapies

    • Contribute to Global Clinical Study Programs across JAPAC Region

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  • 日本
    正社員
    外資系企業
    • Manage all aspects of clinical trial - handle site management and monitoring activities for assigned Phase I and all Phase II-IV clinical Investigator sites within approved Clinical Development Plan


    • Contribute to effective and safe management of trials with maximum efficiency to ensure best clinical outcomes

    • Work for a Well-known European Pharmaceutical Company

    • Contibute to Development of Life-changing Medicines

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  • Pharmacovigilance Operations Specialist - Global CRO
    日本
    正社員
    外資系企業
    • Responsible for the following Case processing tasks as a member of the clinical information or post-marketing drug or medical device safety information management project:

      - Receipt of information on adverse events, entry in database
      - Creation of case description (Japanese, English)
      - Primary evaluation of the necessity of reporting a defect to PMDA
      - Creation of adverse drug report
      - QC check

    • Develop Innovative New Drugs at a Leading Global Contract Research Organization

    • Contribute the Safety and Wellness of Patients Globally

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  • 東京都
    正社員
    外資系企業
    • Responsible for management of clinical trials including feasibility, oversight of monitoring (including CRO), supervision of site, formulation and implementation of clinical operation plan , selection of clinical trial site, quality control, cost control and risk management, smooth operation of clinical trial team (including outsourced vendor), review of clinical trial SOPs, collaboration with overseas personnel in international joint trials

    • Contribute to Clinical Execellence at a Global Leader in the Pharma Industry

    • Build on your Expertise in Clinical Site Management at a Regional Level

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