The Association of Clinical Research Professionals

Webinar—Investigator Initiated Trial (IIT) Database Design and Build

Event Date: August 19, 2020, 12:00-1:00 PM ET

Registration Deadline: August 18, 2020 11:59 PM ET

Speaker:

  • Samantha Sharpe, CCRP, Clinical Research Project Manager, Nationwide Children’s Hospital
  • Alexandria Alfarano, ACRP-CP, Clinical Research Project Manager, Nationwide Children’s Hospital

Pricing With Contact Hours

Member: $15 | Nonmember: $75

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This course is approved for 1.0 ACRP contact hours. Accreditation Details


Pricing Without Contact Hours

Member: $0 | Nonmember: N/A

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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.

Learning Objectives:

  1. Introduce basic database design principles and formats.
  2. Describe process of converting protocol events into data points.
  3. Highlight common data management tips and tricks.