ICH E6

ICH E6 (R3) – Investigator

Step into the shoes of Dr. Kiran Sharma for a guided tour through the multifaceted responsibilities of a Clinical Trial Investigator at the core of medical innovation. Using ICH E6 R3 GCP as our guide, we’ll explore the investigators’ lead role in furthering new treatments while safeguarding participant well-being. We’ll also learn about an investigator’s essential duties, including careful protocol execution, managing the informed consent process, stringent reporting requirements, and comprehensive trial oversight. You’ll come away with a strong understanding of a Clinical Trial Investigator’s complex and essential responsibilities.

CEU Credits: 0.1
Course Code: ELM-982
Duration: 15 mins
Skill Level: Intermediate
Language: English
Final Exam: Yes
Certification: Yes
Version: V1.0
Effective Date: 07/21/2025

Curriculum for this course

Good Morning
What an Investigator Does
Clinical Trial Site Leaders
Investigator Qualifications
Staffing and Resourcing
Medical Oversight and Participant Welfare
Compliance
Informed Consent and Assent
IMP Management & Accountability
Randomization & Blinding
Records and Reports
Trial Termination
Computerized System Oversight
Reports
The Core of An Investigator
Test your Knowledge!
v1.0 Course released on 09/30/2025

Courses

Browse our extensive catalog of GxP, Corporate Compliance and EH&S training.

Learning Strategy

Boost your organization’s training with LearnGxP’s Learning Strategy Consultants (LSC). They customize learning paths to match your needs, offering ongoing support for lasting success.

Customer Stories

Discover how LearnGxP addresses real challenges, provides effective solutions, and positively impacts our customers’ organizations.