Training

All of the trainings listed below are available in person and through ACME but must be requested using the appropriate request form below. 

 

In-Person Training Request Form    ACME Training Request Form

 

List of Available Trainings

Basics of Informed Consent (Elements of a Successful Informed Consent)

Creating Data Collection Forms

Study Close-out Activities

Typical Informed Consent Mistakes and How to Address Them Part I

Typical Informed Consent Mistakes and How to Address Them Part II

Study Errors Noted During Audits and How to Correct Them

Budget Preparation Training

Basic iRIS Features and Submissions

Facilitate Contract and Budget Negotiations

Basics of Advertisements and Subject Recruitment

Building a Regulatory Binder

Basics of ClinicalTrials.gov 

Training requirements for PIs and Research Staff

What are SAEs and AEs and How Should We Report Them 

Research Misconduct and EthicsPoint 

Preparing for External Audits (FDA, NIH, Sponsor) 

Basics of Data Collection & Data Management 

How to Prepare for an Internal Research Audit

If you have any ideas for trainings that you would like to see, please feel free to email jackie.roberts@ttuhsc.edu with your comments.