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organization, equipment, and supply inventories while supporting a productive and collaborative research environment. Ensure compliance with institutional, federal, and state regulations, including IRB, IACUC
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members, staff, outside experts, and community representatives, and these committees are administered by the Office of Research Services. What You'll Do: Work independently on duties related to the IRB
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IRB applications, clinical data collection, drafting DSMB minutes, data quality management, performing lab experiments such as ELISA and colorimetric assays, biospecimen processing, shipping and storing
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Posting Summary Logo Posting Number RTF00003PO26 USC Market Title Research Specialist Link to USC Market Title https://uscjobs.sc.edu/titles/156405 Business Title (Internal Title) Research Assistant
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Review Committee (SRC), Institutional Review Boards at Fred Hutch and University of Washington (IRBs), Clinical Research Budget and Billing (CRBB), Office of Sponsored Programs (OSP) and Industry Sponsors
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employer, contributing $7 billion annually to the local economy and $8 billion statewide. To learn more about UC Irvine, visit www.uci.edu . Visit our department website here, https://www.uciortho.com/ Your
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numbers with applicable study IRB numbers for tracking and reporting purpose. Maintains an updated list of payment contacts for all studies and funding sources, as applicable. Monitors study payment
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requirements for investigational drug use. Maintain study specific files. Dispense, compound, and package investigational drugs upon written order of investigator, and according to the IRB approved protocol
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regulations, IRB requirements, and institutional SOPs. -Provide guidance on protocol development, IRB planning, safety considerations, and ethical research conduct. -Lead data quality systems, monitoring plans
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with other centers, PIs, collaborating groups, etc., to facilitate collaboration and exchange of information for planning purposes Assures adherence to grant, IRB and WashU accounting, and department