Training

All of the trainings listed below are available in person and through ACME and must be requested using the request form. Click on the button below to open the Training Request Form.

Training Request Form

 

List of Available Trainings

Basics of Advertisements and Subject Recruitment

Basics of ClinicalTrials.gov

Basics of Data Collection & Data Management 

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

Basic of iRIS Features and Submissions

Budget Preparation Training

Building a Regulatory Binder

Creating Data Collection Forms

Facilitate Contract and Budget Negotiations

How to Prepare for an Internal Research Audit
Online Informed Consent Training
Preparing for External Audits (FDA, NIH, Sponsor) 
Research Misconduct and EthicsPoint 

Study Close-out Activities

Study Errors Noted During Audits and How to Correct Them

Training Binder Development Training

Training Requirements for PIs and Research Staff

Typical Informed Consent Mistakes and How to Address Them Part I

Typical Informed Consent Mistakes and How to Address Them Part II

What are SAEs and AEs and How Should We Report Them 

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.