Investigator Initiated Trial (IIT) Database integrity

When:  May 3, 2021 from 5:00 PM to 6:30 PM (MT)
Associated with  ACRP Front Range Chapter

Designing meaningful case report forms (CRFs) and building databases for an Investigator-Initiated Trial (IIT) can be a dizzying process. In this webinar series, you’ll learn how to turn your protocol into a fully functional database, translate study objectives into data points that make it easier to manage and analyze your data, and clean and monitor data points throughout the course of the study. Whether you’re an investigator, research coordinator, a project manager, or even a monitor, these webinars are for you. Join us for two detailed presentations full of helpful tips to get you started! You’ll get access to some of our best tips and tricks and learn how to avoid common pitfalls; we’re even sharing helpful checklists and documents that you can take with you.

This event is an ACRP webinar replay

Speakers: Samantha Sharpe, CCRP,
                  Clinical Research Project Manager, Nationwide Children's Hospital
                  Alexandria Alfarano, ACRP-CP,
                 Clinical Research Project Manager, Nationwide Children's Hospital

Target Audience:

  • CRCs
  • CRAs
  • Investigators
  • Project Managers
  • Regulatory Affairs/Compliance
  • Data Managers (Site, Sponsor, CRO)
  • Clinical Research Administrators
Program Agenda:
4:45 PM – 5:00 PM - Registration & Sign-in
5:00 PM – 6:00 PM - Presentation
6:00 PM – 6:15 PM - Q&A

Learning Objectives:
  1. Discuss how ALCOA-C principles apply to database design.
  2. Introduction of data analysis terms and management techniques.
  3. Present tips to increase utility to get the most out of a IIT database.


Click here to purchase the contact hour.

Location

Dial-in Instructions:
Please send an e-mail to the person listed as the contact for this event to receive the Zoom instructions.
Event Image

Contact

Laurie Burnside
3037221414
Laurie.Burnside@outlook.com