Clinical Trial Basics Workshop
Tuesday April 20, 2010
8:45 AM - 5:00 PM
Crowne Plaza Hotel, Foster City CA
$389 by April 6, 2010
$449 thereafter
Each attendee will receive:
An overview of clinical trials
An understanding of key abbreviations
Interactive learning exercises
9 BRN contact hours
Continental breakfast
Luncheon
Prizes for participation
Presented by Tricia Cheney and Patty Kasper
Clinical Research Consultants
Register today at www.PKasperAssociates.com
This one-day course has been designed to provide an overview of the clinical trial process for research nurses, coordinators and drug development professionals who want to expand their understanding of clinical research. It is ideal for individuals supporting the bio-pharmaceutical industry in functions such as CRA Assistant, Clinical Research Coordinator, or Administrative Assistant.
The following topics are presented in a lecture and exercise format
Overview of Clinical Trials
Phases of Drug Development
Types of Clinical Trials
Protocols/Case Report Forms
Informed Consent
Adverse Events
Study Medication/Supplies Identifying/Selecting Investigators
Study Budgets
Regulatory Documentation
Institutional Review Boards
Site Monitoring Visits
Data Management
At the completion of the course the participant will be able to
Describe the basics of clinical research
Recognize FDA and regulatory requirements
Assess protocols, case report forms and consents
Identify and track investigator and financial documents
Evaluate paperwork required in this regulated environment
