Intermediate CRC Training Seminar

This seminar is designed for clinical research coordinators (CRCs) and clinical investigators with more than 18 months of experience conducting clinical trials. Intermediate CRC training goes beyond the material presented in Fundamentals of Clinical Research to include in-depth coverage of informed consent, study budgets, and principles of written communication. Enrollment is limited to 45 participants.

Upcoming Dates & Locations

• San Diego, Aug. 8-9
• Houston, Oct. 18-19

Course Objectives

By attending this course, participants should be able to:

• Write a consent form for investigational research that is compliant with federal regulations.
• Identify the elements of a study budget, and develop reasonable and profitable study budgets.
• Evaluate the benefits of running research as a business through assertive marketing and appropriate allocation of time and resources.
• Develop standard operating procedures for clinical sites.
• Explain techniques to communicate more effectively with sponsor representatives through verbal and written communication.
• List six advertising mediums for study patient recruitment.
• Describe the means to prepare for an FDA audit.
• Discuss implications of FDA audit findings.