Training
The Research Compliance Unit offers trainings for TTUHSC EP clinical research personnel,
designed to help prepare and guide staff through a human subject clinical research
study.
Please note that all of the trainings offered are focused solely on human subject
clinical research.
Below are the trainings offered, along with a brief description.
Click Here to Request Training
* Please note that in-person trainings are not being offered at this time.
* If you have any ideas for trainings that you would like to see, please feel free
to email your request to Research Compliance elp-researchcompliance@ttuhsc.edu.
| Trainings Offered | Online Training |
|---|---|
| Required Courses | |
| Basic Informed Consent Training *Required by the IRB to obtain or maintain an iRIS account if you will be conducting human subject research* Basic introduction to conducting informed consent for clinical research purposes. |
Available |
| Introduction Courses | |
| Training Requirements for Clinical Research Personnel An introduction to the basic training requirements for PIs and research personnel. |
Available |
| What is iRIS and How Do I Get an Account? An introduction to the iRIS software and how to request a user account. |
Available |
| Building a Study Regulatory Binder An introduction to regulatory binders, their purpose, and how they are built. |
Available |
| Creating and Maintaining Data Collection Forms A basic introduction to creating and maintaining research forms created for specific studies. |
Available |
| Basics of Data Collection & Data Management A basic introduction to aid faculty and staff in collecting and maintaining data for clinical research trials. |
Available |
| Training Binder Development and Other Helpful Tools Helpful tools for organizing and maintaining research and departmental records. |
Available |
| Basics of ClinicalTrials.gov Basic introduction into ClinicalTrials.gov that is meant to aid research personnel in determining if a clinical trial should be submitted to ClinicalTrials.gov. |
Available |
| Study Advertisements and Subject Recruitment A review of the types of advertisements that can be used to recruit subjects and what information is required. |
Available |
| Research Misconduct A training to familiarize research faculty and staff with typical forms of research misconductand what to do if they come across it. |
Available |
| What are Unanticipated events and How Should They Be Reported (AE, SAE, UPIRSO…)? A basic introduction to identifying and reporting unanticipated events such as adverse events and serious adverse events for clinical research purposes. |
Available |
| Preparing for Internal Research Audits A basic introduction to aid faculty and staff in preparing for an audit in order to know what to expect. |
Available |
| Preparing for External Research Audits A basic introduction to aid faculty and staff in preparing for and in knowing what to expect for external audits. |
Available |
| Basics of Data Collection for Retrospective Cart Review A basic introduction to aid faculty and staff in collecting and maintaining data for retrospective chart review studies. |
Available |
| Typical Audit Findings for Retrospective Studies Typical audit findings for retrospective chart review studies and how to prevent them. |
Available |
| Basics of Conducting a Retrospective Chart Review Study | Available |
| Informed Consent Process Do's and Don'ts | Available |
| Practice Courses | |
| Typical HIPAA Mistakes A practice course that provides a basic understanding of common mistakes that occur onHIPAA in informed consent forms and how to correct them. |
Available |
| Typical Assent Mistakes A practice course that provides a basic understanding of common mistakes that occur on assents and how to correct them. |
Available |
| Typical Biomedical Informed Consent Mistakes A practice course that provides a basic understanding of common mistakes that occur on biomedical informed consents and how to correct them. |
Available |
| Typical Parental Informed Consent Mistakes A practice course that provides a basic understanding of common mistakes that occur on parental informed consents and how to correct them. |
Available |
| Atypical Informed Consent Scenarios Scenario training for principal investigators and research staff using informed consents. |
Available |