Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena.
Responsibilities:
·Bachelor’s degree required or equivalent combination of education and experience.
·Medical and/or science experience/education preferred.
·Clinical research certification preferred.
Equal Opportunity Employer of Minorities/Females/Disabled/Veterans
Clinical Research Coordinator II • Michigan, Detroit
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