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  • Clinical Research Associate

    IQVIA —Brighton

    Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF)…

  • IQVIA —Reading

    Requires at least 2 years on-site monitoring experience of interventional studies. Ensure copies/originals (as required) site documents are available for filing…

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