The Association of Clinical Research Professionals

eResearch: Managing Clinical Trials in an Electronic Environment

Contact Hours: 1.5 (ACRP, CBRN, ACCME)

Member: $99 | Non-Member: $149

Register

This eLearning course will be accessible for up to one year from the date of purchase.

More and more companies are going “paperless.” What does this mean in the field of clinical research?

This online course examines the challenges of working with electronic documents and how to overcome them. Learn how to set up and manage electronic clinical research documents in compliance with U.S. and EU regulations, and current trends from both the site and sponsor perspectives.

Job aids in the form of compliance checklists (CDISC user requirements and site-level electronic records compliance) and website references are included to ensure you achieve achieve compliance in a paperless clinical trial environment.

Learning Objectives

  • Apply regulations and guidance related to the management and use of electronic tools in clinical research
  • Evaluate the use of electronic tools and electronic medical records (EMRs) by sites and sponsors during clinical trials
  • Employ “best practices” for the completion and monitoring of electronic case report forms (eCRFs) and electronic informed consent forms (eICFs) based on multiple electronic source documents

Audience

Clinical Research Professionals that work with electronic trial documents.

Bring this Program to Your Team!

Bring the quality and effectiveness of this program to your entire clinical research team! We’re ready to help you achieve your organization’s goals and promote excellence in clinical research. Get in touch today and we’ll get started!

Jenna Rouse

Director, Business Development
Talent Onboarding & Staff Development
+1.703.254.8109

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