September 2017 - July 2018

2017-2018 Video and Handout Archive

This portion of the IPPCR website is for all enrolled participants, on site, and remote site. There is no attendance requirement for the IPPCR course. Participants are free to watch the videos at their convenience.

The Exam is currently unavailable.

Module 0 - Introduction
09/17/2017 Welcome and a History of Clinical Research: A Merging of Diverse Cultures
Dr. John I. Gallin
FAQ
Module 1 - Study Design, Measurement, and Statistics
Unit 1:
09/18/2017
Choosing a Research Question and Implications for Efficient Clinical Trials
Dr. John Powers, III
FAQ
Unit 2:
09/18/2017
Overview of Clinical Study Design
Dr. Laura Lee Johnson
FAQ
Unit 3:
09/18/2017
Design of Epidemiologic Studies
Dr. Laura Lee Johnson
FAQ
Unit 4:
09/18/2017
Clinical Research from the Patient's Perspective and Study Participant Selection
Mr. Jerry Sachs and Dr. Catherine Stoney
FAQ
Unit 5:
09/18/2017
Issues in Randomization
Dr. Paul Wakim
FAQ
Unit 6:
09/18/2017
Overview of Hypothesis Testing
Dr. Paul Wakim
FAQ
Unit 7:
09/18/2017
Sample Size and Power
Dr. Laura Lee Johnson
FAQ
Unit 8:
09/18/2017
Conceptual Approach to Survival Analysis
Dr. Laura Lee Johnson
FAQ
Unit 9:
09/18/2017
Measures
Dr. David Luckenbaugh
FAQ
Unit 10:
09/18/2017
Quality of Life
Dr. Kevin Weinfurt
FAQ
Unit 11:
09/18/2017
Designing and Testing Questionnaires
Ms. Barbara Stussman
FAQ
Unit 12:
09/18/2017
Using Large Datasets for Population-Based Health Research
Dr. Leighton Chan
FAQ
Unit 13:
09/18/2017
Secondary Data/Meta-Analysis
Dr. Charles Natanson
FAQ
Unit 14:
09/18/2017
Module I Summary and Study Examples
Dr. Laura Lee Johnson
FAQ
Module 2 - Ethical, Legal, Monitoring, and Regulatory Considerations
Unit 15:
09/18/2017
Legal Issues in Clinical Research
Mrs. Carrie Kennedy
FAQ
Unit 16:
09/18/2017
Ethical Principles in Clinical Research
Dr. Christine Grady
FAQ
Unit 17:
09/18/2017
Data and Safety Monitoring Committees
Dr. Pamela Shaw
FAQ
Unit 18:
09/18/2017
Institutional Review Boards
Dr. Jerry Menikoff
FAQ
Unit 19:
09/18/2017
Mock IRB
Dr. Jerry Menikoff
FAQ
Unit 20:
09/18/2017
Research with Vulnerable Participants
Dr. David Wendler
FAQ
Module 3 - Preparing and Implementing Clinical Studies
Unit 21:
09/18/2017
Developing Protocols and Manuals of Operating Procedures
Dr. Wendy Weber
FAQ
Unit 22:
09/18/2017
Evaluation of a Protocol Budget
Ms. Phyllis Klein
FAQ
Unit 23:
09/18/2017
Scientific Conduct
Dr. James L. Gulley
FAQ
Unit 24:
09/18/2017
Inclusion of Women and Minorities in Clinical Trials
Janine Austin Clayton and Meredith D Temple-O'Connor
FAQ
Unit 25:
09/18/2017
Pharmaceutical Development: Management of Projects
Dr. Christopher Breder
FAQ
Unit 26:
09/18/2017
NIH Peer Review Process
Dr. Valerie Prenger
FAQ
Unit 27:
09/18/2017
FDA Product Regulation
Dr. Chris Joneckis
FAQ
Unit 28:
09/18/2017
Data Management & Case Report Form Development in Clinical Trials
Ms. Marge Good
FAQ
Unit 29:
09/18/2017
Electronic Health Records and Clinical Data Interchange Standards
Dr. Stephen Wilson
FAQ
Unit 30:
09/18/2017
Quality Management in Clinical Research
Ms. Elizabeth Ness
FAQ
Unit 31:
09/18/2017
Clinical Trial Registration and Results Reporting
Dr. Deborah Zarin
FAQ
Unit 32:
09/18/2017
Information Resources for Clinical Research
Mr. Josh Duberman
FAQ
Module 4 - Module 4: Additional Study Designs and Miscellaneous Topics
Unit 33:
09/18/2017
Technology Transfer
Mr. Bruce Goldstein
FAQ
Unit 34:
09/18/2017
Dissemination and Implementation Research
Dr. Catherine Stoney
FAQ
Unit 35:
09/18/2017
Health Disparities Research
Dr. Larissa Aviles-Santa
FAQ
Unit 36:
09/18/2017
Health Disparities and Community-Based Participatory Research
Dr. Tiffany M. Powell-Wiley
FAQ
Unit 37:
09/18/2017
The Clinical Researcher and the Media
Mr. John Burklow
FAQ