PRAHS

  • Clinical Research Associate 3

    Job Locations (All) | Colombia
    Posted Date 2 weeks ago(12/5/2018 5:11 PM)
    ID
    2018-50892
  • Overview

    The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

    Responsibilities

    Read, write and speak fluent English; fluent in host country language required.
    •Knowledge of ICH and local regulatory authority regulations regarding drug
    •5+ years of clinical monitoring experience required
    •Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required

    Qualifications

    •Clinical research experience
    •Knowledge of ICH and local regulatory authority regulations regarding drug
    •An advanced degree (e.g., M.S., M.B.A., PharmD, etc)
    •Experience in monitoring complex trials
    •Participation in departmental initiatives
    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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