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include recruiting and consenting study participants in compliance with IRB protocols; assisting in the distribution and collection of surveys; supporting the conduct and transcription of qualitative
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on using unstructured and overset meshes with high-fidelity algorithms to obtain scale-resolved data. Candidate will also post-process data using data-driven and physics-driven methods to extract fundamental
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distribution, addressing non-clinical barriers preventing engagement with the health system and utilizing inclusion and exclusion criteria for participation in the clinical services and research studies
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(East and Main campus) for various health related services such as OUD/SUD, HIV testing, HCV education, harm reduction education, naloxone distribution, addressing non-clinical barriers preventing
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assistance in support of a research program; assists with maintaining research supply inventory and orders supplies as needed; picks up, sorts, and distributes mail; make copies and files; run errands
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protocol; distributes and explains processes and goals of clinical studies to participants; assists with development of clinical study informational and educational materials; assists with informed consent
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protocol; distributes and explains processes and goals of clinical studies to participants; assists with development of clinical study informational and educational materials; assists with informed consent