Research Education Schedule and Registration

Clinical Research Education Available On-Demand in UH GPS

Required and General

• UH Investigator Training
• Investigator and Study Team Responsibilities
• Getting Started With Your Research
• Introduction to Common Rule Changes
• IRB: Continuing Review Submissions
• Identifying & Managing Conflicts of Interest in Research

The Basics

• Module 1: FDA Federal Regulations and Good Clinical Practice (GCP)
• Module 2: Required Regulatory Documentation & Essential Documents
• Module 3: Study Feasibility through Study Activation
• Module 4: Research Finance: Coverage Analysis and Research Billing Compliance
• Module 5: Prescreening, Eligibility & Enrollment Process
• Module 6: Informed Consent & Re-consent
• Module 7: Good Documentation Practices & Clinical Data Management
• Module 8: Adverse Events & Protocol Deviations
• Module 9: Avoiding Non-Compliance Findings

Clinical Research SOP Training

• SC 410 - Certified Copies of Research Regulatory Documents
• GA 109 - Departing Investigators
• GA 110 - Management of Clinical Research
• SS 307 - Obtaining an Identified Patient List Through the UH Clinical Research Center’s TriNetX Export ID Feature