Clinical Trials Management Training
The Clinical Trial Management Training program was conceived and designed by pharmaceutical, biotechnology and contract experts who work in the clinical research field; it is intended for learners who seek entrance or advancement in the clinical research industry.
Students learn the fundamentals of the clinical trial environment, and study design and management. The program prepares students for day to day decision making in their work environments. Each course is thoroughly designed to enhance drug development knowledge.
Course Descriptions:
- Introduction to Clinical Trial Research and Drug Development
Provides and introduction to the field of clinical research and an overview of the environment, FDA approval processes and regulations, and various elements involved in the development and conduct of clinical research trials. - Clinical Trial Research: Practice and Policy
Provides students with an understanding of clinical research methods, as well as current issues concerning drug and device development in the United States. - Introduction to Clinical Trials Data Management
Provides an overview of the clinical data management process in pharmaceutical research setting. - Ethical Issues and Regulatory Principals in Clinical Trials
Provides a step wise approach to understanding clinical research and how today’s regulations impact tomorrow’s drugs.
