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Overview

Gain the basic knowledge required to conduct clinical trials, including information about subject safety, regulations, and the practicalities of performing research studies.

Course Level: Beginner

What you will learn

  • Roles and responsibilities of each member of the study team
  • Regulations and guidelines that govern clinical investigations
  • Informed consent elements and processes
  • Successful patient recruitment and retention strategies
  • Adverse event handling and reporting
  • Preparing for audits and the audit process

Who should attend?

  • Clinical investigators
  • Clinical research professionals
  • Sub-investigators
  • Study staff

Learning objectives

Participants who complete this training should be able to:

  • Identify the roles and responsibilities of each member of the study team including the clinical investigator, sub-investigator, study staff, IRB, and sponsor
  • Apply the regulations and guidelines for conducting safe and effective clinical trials
  • Describe the various processes for informed consent
  • Describe the requirements in reporting adverse events

Contact us

Jessica McGrory at +1-215-442-6182 or Jessica.McGrory@diahome.org