Clinical Research Center

Research Education Schedule and Registration

Research Seminar Upcoming Events Calendar

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

REDCap: An Introduction

REDCap: Advanced Topics

Velos for Principal Investigators

Velos for Study Coordinators
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