The Association of Clinical Research Professionals

GCP for the Experienced Clinical Research Professional


Member: $189 | Non-Member: $239


This course is approved for 1.5 ACRP contact hours. Accreditation Details

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

Course Description

Take your knowledge and application of ICH E6(R2) GCP to the next level!

Learn about today’s most common inspection findings and proven strategies to avoid them through correct application of the GCP guidelines.

Clinical Research Professionals use this training to:

  • Ensure a solid foundation of knowledge of the ICH E6(R2) GCP Guideline
  • Fulfill employer requirements for GCP training
  • Apply appropriate preventative and/or corrective action following Investigator responsibility-related audit or inspection findings
  • Prepare for an ACRP Certification exam

Learning Objectives

  • Demonstrate qualifications and execute agreements to conduct clinical research with a research sponsor or institute;
  • Provide adequate medical care to a subject throughout the course of a clinical trial;
  • Compose communications with the Institutional Review Board (IRB) or Independent Ethics Committee (IEC);
  • Conduct the trial in compliance with the protocol, including randomization and unblinding procedures;
  • Conduct informed consent procedures according to local regulations, Good Clinical Practice, and principles established by the Declaration of Helsinki; and
  • Develop timely and accurate records and reports.

Competency Domains

This course builds competence in the following domains:

  • Clinical Trials Operations (GCPs)
  • Communication and Teamwork
  • Ethical and Participant Safety Considerations
  • Leadership and Professionalism

Learn About Competency Domains for Clinical Research Professionals >>


All clinical research professionals.