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Clinical Research Associate I/II (Drug Accountability Monitor)
Covance is seeking a CRA to cover the Northeast and West Coast region of the US. This is a specialized CRA role which primarily focuses on drug accountability at a site level across a range of protocols and therapeutic areas. Essential Job Duties: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned Responsible for all aspects of site management as prescribed in the project plans Travel, including air travel, may be required and is an essential function of the job. Prepare accurate and timely trip reports Review progress of
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