October 2014 - March 2015

2014-2015 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
10/14/2014 Welcome
Dr. John I. Gallin
FAQ
10/14/2014 History of Clinical Research: A Merging of Diverse Cultures
Dr. John I. Gallin
FAQ
Module 1 - Study Design and Statistics
Unit 1:
10/20/2014
Choosing a Research Question and Implications for Efficient Clinical Trials
Dr. John Powers, III
FAQ
Unit 2:
10/21/2014
Clinical Research from the Patient's Perspective
Mr. Jerry Sachs
FAQ
Unit 3:
10/21/2014
Study Participant Selection
Dr. Catherine Stoney
FAQ
Unit 4:
10/27/2014
Overview of Clinical Study Design
Dr. Laura Lee Johnson
FAQ
Unit 5:
10/28/2014
Measures
Dr. David Luckenbaugh
FAQ
Unit 6:
11/03/2014
Design of Epidemiologic Studies
Dr. Laura Lee Johnson
FAQ
Unit 7:
11/04/2014
Issues in Randomization
Dr. Paul Wakim
FAQ
Unit 8:
11/10/2014
Using Large Datasets for Population-Based Health Research
Dr. Leighton Chan
FAQ
Unit 9:
11/17/2014
Designing and Testing Questionnaires
Ms. Barbara Stussman
FAQ
Unit 10:
11/18/2014
Overview of Hypothesis Testing
Dr. Laura Lee Johnson
FAQ
Unit 11:
12/01/2014
Sample Size and Power
Dr. Laura Lee Johnson
FAQ
Unit 12:
12/04/2014
Conceptual Approach to Survival Analysis
Dr. Laura Lee Johnson
FAQ
Unit 13:
12/08/2014
Secondary Data/Meta-Analysis
Dr. Charles Natanson
FAQ
Unit 14:
12/09/2014
Module I Summary and Study Examples
Dr. Laura Lee Johnson
FAQ
Module 2 - Ethical, Legal, and Regulatory Considerations
Unit 1:
12/15/2014
Ethical Principles in Clinical Research
Dr. Christine Grady
FAQ
Unit 2:
12/16/2014
FDA Product Regulation
Dr. Chris Joneckis
FAQ
Unit 3:
01/05/2015
Institutional Review Boards
Dr. Jerry Menikoff
FAQ
Unit 4:
01/06/2015
Mock IRB
Dr. Jerry Menikoff
FAQ
Unit 5:
01/12/2015
Research with Vulnerable Participants
Dr. David Wendler
FAQ
Module 3 - Preparing and Monitoring Clinical Studies
Unit 1:
01/13/2015
Data and Safety Monitoring Committees
Dr. Pamela Shaw
FAQ
Unit 2:
01/20/2015
Protocol Development
Dr. Wendy Weber
FAQ
Unit 3:
01/20/2015
Proto Type & Beyond: A History of Electronic Protocol Authoring at the Clinical Center
Mr. Phillip Lightfoot
FAQ
Unit 4:
01/20/2015
Protocol Authoring Tool
Mr. Shashikiran Rudrappa
FAQ
Unit 5:
01/26/2015
Pharmaceutical Development: Management of Projects
Dr. Christopher Breder
FAQ
Unit 6:
01/27/2015
Evaluation of a Protocol Budget
Ms. Phyllis Klein
FAQ
Unit 7:
02/02/2015
NIH Peer Review Process
Dr. Valerie Prenger
FAQ
Unit 8:
02/03/2015
Data Management & Case Report Form Development in Clinical Trials
Ms. Marge Good
FAQ
Unit 9:
02/09/2015
Basic Data Representation
Dr. James Cimino
FAQ
Unit 10:
02/10/2015
Data & Non-Data Aspects of Quality Control in Clinical Studies
Ms. Elizabeth Ness
FAQ
Unit 12:
02/23/2015
Clinical Trial Registration and Results Reporting
Dr. Deborah Zarin
FAQ
Module 4 - Miscellaneous Topics
Unit 1:
02/24/2015
Technology Transfer
Mr. Bruce Goldstein
FAQ
Unit 2:
03/02/2015
Scientific Conduct
Dr. James L. Gulley
FAQ
Unit 3:
03/03/2015
Health Disparities Research
Dr. Larissa Aviles-Santa
FAQ
Unit 11:
03/09/2015
Information Resources for Clinical Research
Mr. Josh Duberman
FAQ
Unit 4:
03/10/2015
Community-Based Participatory Research
FAQ
Unit 5:
03/10/2015
Dissemination and Implementation Research
Dr. Catherine Stoney
FAQ
Module 5 - Lectures To Be Viewed Only On Archives
Unit 1:
10/21/2014
Inclusion of Women and Minorities in Clinical Trials
Dr. Miriam Kelty
FAQ
Unit 5:
01/27/2015
Development of Manuals of Operating Procedures
Dr. Wendy Weber
FAQ
Unit 2:
03/09/2015
Quality of Life
Dr. John Ware
FAQ
Unit 3:
03/09/2015
The Clinical Researcher and the Media
Mr. John Burklow
FAQ
Unit 4:
03/09/2015
Legal Issues in Clinical Research
Mrs. Carrie Kennedy
FAQ