The on-line modules will provide a basic overview of clinical research. The modules were initially developed by the Center for Cancer Research, NCI and have been endorsed by the leadership team of the CTN SIG.

Adverse Events Learning Module (updated May 8, 2009)

Clinical Trial Design

Protocol Development

Managing Data in Clinical Research

Documentation in Clinical Research

Roles and Responsibilities of the Sponsor

Roles and Responsibilities of the Research Team

Regulatory Binder

Informed Consent Process

RECIST: Applying the Rules

Types of Site Visits for Sponsored Clinical Trials