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program and advanced knowledge of methods of analyzing data from experimental platforms. May assist in grant and other funding applications as necessary and appropriate, or with approval of the responsible
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contribute to the excellence of our academic community. The Clinical Research Data Coordinator I supports the research program within the Clinical Trials Office (CTO) of Winship Cancer Institute (WCI) at Emory
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or PhD in a scientific, health related, or business administration program and two years of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC
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oversee quality and training of other team members. Duties include designing, developing and conducting research experiments. Will have expert knowledge and skills specific to the related program and
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. For the qualified candidate, there may be an option to create a personalized program, which could include body imaging as well as general and cardiac nuclear medicine rotations. An option for a second year of
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necessary to advance basic and/or translational research programs. Responsible for working with experimental platforms specific to the hiring Program. Duties will include but are not limited to experimental
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student in a college or university. Completion of freshman year or higher and in good academic standing. PREFERRED QUALIFICATIONS: Currently pursuing a Master’s or PhD in Human-Computer Interaction
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acquisition best practices. Ensure consistent, high-quality instruction and consultation to promote effective and reproducible cytometry experiments. Strategic Planning & Program Development: Lead strategic
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the NICU and participation in student, resident, and fellow education. Qualified candidates must have an MD, MD/PhD, or equivalent and must be board-certified/board-eligible in Neonatal-Perinatal Medicine
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program and one year of clinical research experience. Or a Master's degree, MD or PhD in a scientific, health related or business administration program. This position is intended to support clinical