PRAHS

  • Clinical Data Administrator 1 - Salt Lake City

    Job Locations - | US-UT-Salt Lake City
    Posted Date 8 hours ago(8/17/2018 11:08 AM)
    ID
    2018-48316
  • Overview

    Supports the preparation and conduct of studies by reviewing study data, receiving and tracking study documents and entering data into clinical databases and Case Report Forms (CRFs). Provides support during monitoring visits as well as archiving clinc study documents. 

    Responsibilities

    • May read and understand clinical trial protocols prior to starting any study specific tasks
    • Work actively in project team environment
    • Assist level II with reporting status and quality
    • Oversee the document flow to ensure process is being followed for each study
    • Assist with clinic study set-up activities as needed
    • Assist with source document QC as needed
    • May ensure CRFs and/or electronic CRF database is available prior to the study
    • May participate in the creation and review of CRF/eCRF database
    • May ensure source documents are delivered to the clinic prior to study check in
    • May ensures source documents are QC’ed prior to data-entry
    • Transcribes information from the source documents to CRFs as outlined in the instructions and within specified timelines
    • Assists with query resolution if needed
    • Ensures all filing for studies is complete and according to filing instructions
    • For paper studies ensure that CRFs/DCFs are in order at the end of the study 
    • Assists with archiving tasks as needed 
    • Assists as needed with monitoring visits 

    Qualifications

    • Read, write, and speak fluent English; fluent in host country language
    • 1-2 years work experience preferred



    • High School Diploma, G.E.D., or secondary vocational education required



    • N/A





    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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