
Human Research Protection Program at UMC - Clinical Trials & Nursing Research
Explore the Human Research Protection Program at UMC, including Institutional Review Board, Clinical Trials Office, and Nursing Research. Learn about subjects protection, compliance, and how to get involved in research projects at University Medical Center of Southern Nevada.
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Presentation Transcript
Human Research Protection Program at UMC Institutional Review Board Clinical Trials Office Nursing Research www.umcsn.com UNIVERSITY MEDICAL CENTER OF SOUTHERN NEVADA
Institutional Review Board Human Subjects Protection History of Human Subjects Protection OHRP and FDA Regulations QI vs. Research Types of Research Interventional and Bio-Medical Research Retrospective Research Social Behavioral www.umcsn.com UNIVERSITY MEDICAL CENTER OF SOUTHERN NEVADA
Clinical Trials Office Sponsored Interventional Research Research Billing Compliance Clinical Trial Support Regulatory and Study Support Contract and Budget Negotiations Invoicing and Financials www.umcsn.com UNIVERSITY MEDICAL CENTER OF SOUTHERN NEVADA
Nursing Research IRB Determination Prior to Council Approval CITI Training and Certification Updated CV Request an eIRB Account Get involved with research projects www.umcsn.com UNIVERSITY MEDICAL CENTER OF SOUTHERN NEVADA
Questions www.umcsn.com UNIVERSITY MEDICAL CENTER OF SOUTHERN NEVADA
Contacts Robert Bimbi Clinical Research Analyst (702) 383-7302 robert.bimbi@umcsn.com Robert (RJ) Panganiban Clinical Research Analyst (702) 383-7336 robert.panganiban@umcsn.com jennifer.robinson@umcsn.com Jennifer Robinson Clinical Research Analyst (702) 383-7842 Ronald Roemer Director Clinical Research and Compliance (702) 207-8345 ronald.roemer@umcsn.com https://www.umcsn.com/HRPP/Home.aspx www.umcsn.com UNIVERSITY MEDICAL CENTER OF SOUTHERN NEVADA