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CRA or Senior SCRA Russia (Clinical Research Associate) - Oferta z Jobs.pl

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CRA or Senior SCRA Russia (Clinical Research Associate)

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  • The key responsibilities of a Clinical Research Associate (CRA/SCRA) are to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations, performing clinical on-site monitoring activities, collecting regulatory documentation, performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.

    Responsibilities & Accountabilities of a CRA/SCRA:

    • Take responsibility for specific tasks on projects, or acts as the main CRA/SCRA contact on individual projects
    • Strong regulatory knowledge including GCP
    • Strong computer and internet skills including knowledge of MS-Office products such as Excel & Word.
    • Train team members on selected tasks

    A successful CRA/SCRA candidate will:

    • Have substantial monitoring experience within the field of clinical research
    • Be educated to a degree level in a life science
    • Be competent in both written and oral English
    • Have the ability to complete tasks in an accurate and timely manner.

    If you are interested in this role, please send your CV to with your availability, or for a confidential conversation about the role please contact Simon on .

    Key Skills:

    Clinical Research Associate, CRA, CRA 1, CRA 2, Senior Clinical Research Associate, SCRA, CRA II, CRA I, Russia CRA, Global CRA, European CRA, Justpharma, Just Pharma, Monitoring, Clinical Trial, Drug Trial, Trial Sites, Clinical, Clinical research, Moscow, Russia


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