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Clinical Research Associates CRA II/SCRA - in the Czech Republic - Oferta z Jobs.pl

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Clinical Research Associates CRA II/SCRA - in the Czech Republic

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  • The key responsibilities of a Clinical Research Associate (CRA) 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:

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

    A successful candidate will:

    • Be educated to a degree level in a life science
    • Be competent in both written and oral English
    • Have substantial monitoring experience within the field of clinical research

    For further information on this position or to have a confidential conversation please contact Simon on (0) or email

    Key Skills:

    Clinical Research Associate, CRA, Senior Clinical Research Associate, SCRA, Justpharma, Just Pharma, Monitoring, Clinical Trial, Drug Trial, Trial Sites, Czech Republic, Prague, Monitor, Clinical Research.


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