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. In this role, you will join the consenting team and be responsible for obtaining patient consent through both in-person and electronic consent processes, fulfilling clinical trial requests, supporting
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assessments, and maintaining accurate source documentation. Collect, enter, review, and maintain clinical research data in electronic data capture systems and study databases, ensuring data quality
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attendance. Capacity for flexibility and adaptability in different work situations. Comfort with their own body and examinations by health personnel. Basic computer skills for email communication, document
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. The Marcus Center for Cellular Cures (MC3) https://marcuscenter.duke.edu/ has an exciting growth opportunity for a motivated individual to fill a Cord Blood Collector in their Carolinas Cord Blood
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array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/ Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed
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comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https
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to advance clinical and translational research initiatives. Drive Study and Site Excellence Utilize clinical research systems, electronic health records, OnCore, eREG, and related platforms to manage study
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a variety of channels, including: Websites Videos Case studies Social media campaigns Email marketing communications Articles and graphics Ensure brand consistency and effective storytelling across
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discover how we can advance health together. Duke Health Integrated Practice https://careers.dukehealth.org/us/en/dhip Duke Health Integrated Practice comprises more than 110 primary and specialty outpatient
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coordinating clinical research studies. Experience with IRB submissions, regulatory compliance, and sponsor communications. Familiarity with OnCore, Epic/Maestro Care, REDCap, eREG, and electronic data capture