This course explains the key roles and responsibilities of all major stakeholders involved in clinical research. It covers the duties of investigators, sponsors, vendors, IRBs, and clinical research staff, with a strong focus on ethics, compliance, and regulatory requirements.

Learners will understand how these roles work together to protect study participants and ensure data quality.

The course also highlights Good Clinical Practice (GCP) principles and applicable guidelines. It is designed to give professionals a clear and practical understanding of accountability throughout the clinical trial process.

International students: Click here to Pay the Fee for this course in US dollars.