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Apr 24, 2006 8:00 AM - Dec 31, 2050 12:00 AM

Good Clinical Practices for the Clinical Research Professional


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

Who should attend?

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

Learning objectives

At the conclusion of this activity, participants 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

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