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Latest Jobs

2 listing(s) available.

  • 04 Sep 2020

    SAS Programmer/ SAS 統計編程師

    Taiwan

    Permanent Position
    A global CRO company which provide full-function service in the clinical trial industry

    Job Description

    1. 根據與生物統計的規劃和與生物統計人員的討論後來按照規範去編寫統計程序。
    2. 若您足夠資深, 會負責領導編程項目團隊, 方法是分配任務,審查他們的程序,並與業務合作夥伴和客戶一起為所有可交付成果確定時間表。 若為經驗普通的程式成員, 則按照資深同事的引領進行操作。
    3. 將規範轉換為SAS Code 以生成數據集以及表,清單和圖形輸出。
    4. 分析SAS Code 以查找錯誤原因並修訂程序。
    5. 編寫並維護有關SAS Code,程序和規格更改的文檔。
    6. 修訂程序以進行更正,增強或更改系統環境。
    7. 與其他程序員協調程序修訂。
    8. 修改和維護他人編寫的SAS Code。
    9. •遵循部門質量控製程序的數據集, Table、List、Figure 的質量控制。
    10. 指導新員工和所有級別的SAS Programmer。
    11. 遵循既定的標準化設計和編程程序;為初級SAS Programmer提供指導;協助建立標準化的編程程序和工作指導書;開發、增強、評估和驗證標準化的宏和實用程序;確保通過驗證/合規活動滿足法規要求。
    12. 創建統計分析輸出以用於最終報告、摘要、手稿和其他臨床出版物的支持;支持系統以生成電子監管文件。


    薪水優於經常性薪資

    Expires on 04 Oct 2020

    Posted By

    Steven Yang

    Tel: +886 987 957 235

    stevenyang@peoplesearch.jobs

    Requirements

    • Bachelor's Degree in Biotechnology, Epidemiology, Statistics, Pharmacology or another related science or mathematics field with a minimum of 1-2 years of SAS programming experience with clinical trial data.

     

  • 04 Sep 2020

    [生物統計副處長] Clinical Biostatistical Associate Director

    Taiwan

    Permanent Position
    A Taiwanese local biotech_Independent research and development of new military drugs, clinical trials, cGMP manufacturing, and commercial mass production are all in Taiwan

    Job Description

    1. Utilizing your expertise to conducting and supporting internal SOPs standards, and managing technical quality and consistent approaches in clinical study design and statistical analysis strategically.
    2. Providing input for clinical publications, Clinical Summary of Safety, Clinical Summary of Efficacy, Clinical Overviews and regulatory documents.
    3. You need to plan and execute statistical contributions to Clinical Study Protocols and Clinical Study Reports.
    4. Collaborate with your vendors and colleague, you need to leading the team to perform statistical and exploratory analysis of clinical studies/projects and developing conclusions and recommendations.
    5. Anticipating and communicating resource and quality challenges that could impact deliverables or timelines.
    6. Ensuring the process improvements and operational efficiencies.
    7. Support PV (Drug Safety) function to maintain their safety data preparation and regulatory submission.
    Expires on 04 Oct 2020

    Posted By

    Steven Yang

    Tel: +886 987 957 235

    stevenyang@peoplesearch.jobs

    Requirements

    1. Possesses over 5 years' experience in the Pre-clinical Development, Clinical Development and Post-marketing) filed. 
    2. Obtain strong statistical leadership and contribution to regulatory and reimbursement submissions.
    3. Experience working effectively in a globally dispersed team(US, EU, JP, CN is a preferred) environment with cross-cultural partners.
    4. Experience with data management and PV, especially in having experience of using SAS, SPSS, ADMOS,Argus will be a plus.

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