The Association of Clinical Research Professionals

GCP for the Experienced CRC: Partnering with Your Investigator to Reduce Risk and Avoid Common Inspection Findings


Member: $189 | Non-Member: $239

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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

Execute clinical trial-related agreements, conduct trials in compliance with protocol and GCP, and develop timely and accurate reports as delegated by your PI.

Take your knowledge and application of ICH E6(R2) GCP to the next level! Improve study coordination, reduce risk of inspection findings, attract more clinical trials to your Investigator’s research site and increase your value as a site staff member with this advanced GCP eLearning course.

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

Site personnel and their employers 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

  • Support an Investigator to fulfill his/her responsibilities*
  • Demonstrate qualifications necessary to support a clinical trial
  • Compose communications with an IRB/IEC*
  • Conduct a trial in compliance with the protocol *
  • Conduct informed consent procedures according to local regulations, GCP and principles established by the Declaration of Helsinki*
  • Maintain essential documents*
  • Develop timely and accurate records and reports*
  • Define Adverse Events and Serious Adverse Events

*As delegated by a PI.

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 >>


Clinical research professionals who work at clinical trial sites.