September 2016 - May 2017

2016-2017 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.

Module 0 - Introduction
09/12/2016 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:
09/12/2016
Choosing a Research Question and Implications for Efficient Clinical Trials
Dr. John Powers, III
FAQ
Unit 2:
09/12/2016
Overview of Clinical Study Design
Dr. Laura Lee Johnson
FAQ
Unit 3:
09/12/2016
Design of Epidemiologic Studies
Dr. Laura Lee Johnson
FAQ
Unit 4:
09/12/2016
Clinical Research from the Patient's Perspective
Mr. Jerry Sachs
FAQ
Unit 5:
09/12/2016
Study Participant Selection
Dr. Catherine Stoney
FAQ
Unit 6:
09/12/2016
Issues in Randomization
Dr. Paul Wakim
FAQ
Unit 7:
09/12/2016
Overview of Hypothesis Testing
Dr. Paul Wakim
FAQ
Unit 8:
09/12/2016
Sample Size and Power
Dr. Laura Lee Johnson
FAQ
Unit 9:
09/12/2016
Conceptual Approach to Survival Analysis
Dr. Laura Lee Johnson
FAQ
Unit 10:
09/12/2016
Measures
Dr. David Luckenbaugh
FAQ
Unit 11:
09/12/2016
Quality of Life
Dr. Kevin Weinfurt
FAQ
Unit 12:
09/12/2016
Designing and Testing Questionnaires
Ms. Barbara Stussman
FAQ
Unit 13:
09/12/2016
Using Large Datasets for Population-Based Health Research
Dr. Leighton Chan
FAQ
Unit 14:
09/12/2016
Secondary Data/Meta-Analysis
Dr. Charles Natanson
FAQ
Unit 15:
09/12/2016
Module I Summary and Study Examples
Dr. Laura Lee Johnson
FAQ
Module 2 - Ethical, Legal, Monitoring, and Regulatory Considerations
Unit 1:
09/12/2016
Legal Issues in Clinical Research
Mrs. Carrie Kennedy
FAQ
Unit 2:
09/12/2016
Ethical Principles in Clinical Research
Dr. Christine Grady
FAQ
Unit 3:
09/12/2016
Data and Safety Monitoring Committees
Dr. Pamela Shaw
FAQ
Unit 4:
09/12/2016
Institutional Review Boards
Dr. Jerry Menikoff
FAQ
Unit 5:
09/12/2016
Mock IRB
Dr. Jerry Menikoff
FAQ
Unit 6:
09/12/2016
Research with Vulnerable Participants
Dr. David Wendler
FAQ
Module 3 - Preparing and Implementing Clinical Studies
Unit 1:
09/12/2016
Developing Protocols and Manuals of Operating Procedures
Dr. Wendy Weber
FAQ
Unit 2:
09/12/2016
Evaluation of a Protocol Budget
Ms. Phyllis Klein
FAQ
Unit 3:
09/12/2016
Scientific Conduct
Dr. James L. Gulley
FAQ
Unit 4:
09/12/2016
Inclusion of Women and Minorities in Clinical Trials
Janine Austin Clayton and Meredith D Temple-O'Connor
FAQ
Unit 5:
09/12/2016
Pharmaceutical Development: Management of Projects
Dr. Christopher Breder
FAQ
Unit 6:
09/12/2016
NIH Peer Review Process
Dr. Valerie Prenger
FAQ
Unit 7:
09/12/2016
FDA Product Regulation
Dr. Chris Joneckis
FAQ
Unit 8:
09/12/2016
Data Management & Case Report Form Development in Clinical Trials
Ms. Marge Good
FAQ
Unit 9:
09/12/2016
Electronic Health Records and Clinical Data Interchange Standards
Dr. Stephen Wilson
FAQ
Unit 10:
09/12/2016
Quality Management in Clinical Research
Ms. Elizabeth Ness
FAQ
Unit 11:
09/12/2016
Clinical Trial Registration and Results Reporting
Dr. Deborah Zarin
FAQ
Unit 12:
09/12/2016
Information Resources for Clinical Research
Mr. Josh Duberman
FAQ
Module 4 - Additional Study Designs and Miscellaneous Topics
Unit 1:
09/12/2016
Technology Transfer
Mr. Bruce Goldstein
FAQ
Unit 2:
09/12/2016
Dissemination and Implementation Research
Dr. Catherine Stoney
FAQ
Unit 3:
09/12/2016
Health Disparities Research
Dr. Larissa Aviles-Santa
FAQ
Unit 4:
09/12/2016
Health Disparities and Community-Based Participatory Research
Dr. Tiffany M. Powell-Wiley
FAQ
Unit 5:
02/16/2017
The Clinical Researcher and the Media
Mr. John Burklow
FAQ
Module 0 - Introduction
Lectures that Do Not Belong to a Module:
12/31/1969
FAQ