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The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to maternal health and diabetes
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diabetes prevention. Primary responsibilities include enrolling participants, health coaching, data collection and coordination with other partners within the community. Required Knowledge, Skills, and
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understanding of own personal factors affecting clinical work. Required Education and/or Experience • Master of Social Work degree with current LMSW or LCSW license. • 1 year of clinical experience. OR • Master’s
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