October 2012 - March 2013

2012-2013 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 -
10/16/2012 Welcome
Dr. John I. Gallin
FAQ
10/16/2012 History of Clinical Research: A Merging of Diverse Cultures
Dr. John I. Gallin
FAQ
Module 1 - Study Design and Statistics
Unit 1:
10/22/2012
Overview of Clinical Study Design
Dr. Laura Lee Johnson
FAQ
Unit 2:
10/23/2012
Design of Epidemiologic Studies
Dr. Laura Lee Johnson
FAQ
Unit 3:
11/05/2012
Measures
Dr. David Luckenbaugh
FAQ
Unit 4:
11/06/2012
Secondary Data/Meta Analysis
Dr. Charles Natanson
FAQ
11/06/2012
FAQ
11/08/2012 CANCELLED: OPTIONAL Breakout Session
Dr. Laura Lee Johnson
FAQ
11/12/2012 Federal Holiday
FAQ
Unit 5:
11/13/2012
Study Participant Selection
Dr. Catherine Stoney
FAQ
Unit 6:
11/19/2012
Efficient Clinical Trials
FAQ
Unit 7:
11/20/2012
Issues in Randomization
Dr. Laura Lee Johnson
FAQ
Unit 8:
11/26/2012
Overview of Hypothesis Testing
Dr. Laura Lee Johnson
FAQ
Unit 9:
11/27/2012
Sample Size and Power
Dr. Laura Lee Johnson
FAQ
11/29/2012 OPTIONAL Breakout Session
Dr. Laura Lee Johnson
FAQ
Unit 10:
12/03/2012
Designing and Testing Questionnaires
Dr. Gordon Willis
FAQ
Unit 11:
12/03/2012
Quality of Life
Dr. John Ware
FAQ
Unit 12:
12/04/2012
Conceptual Approach to Survival Analysis
Dr. Laura Lee Johnson
FAQ
12/06/2012 OPTIONAL: Breakout Session
Dr. Laura Lee Johnson
FAQ
Unit 13:
12/10/2012
Using Large Datasets for Population-Based Health Resesarch
Dr. Leighton Chan
FAQ
Unit 14:
12/11/2012
Summary
Dr. Laura Lee Johnson
FAQ
Module 2 - Ethical, Legal and Regulatory Considerations
Unit 1:
12/17/2012
Ethical Principles in Clinical Research
Dr. David Wendler
FAQ
Unit 2:
12/17/2012
Research with Vulnerable Participants
Dr. David Wendler
FAQ
Unit 3:
12/18/2012
Inclusion of Women and Minorities in Clinical Trials
Dr. Miriam Kelty
FAQ
Unit 4:
12/18/2012
Clinical Research From the Patient's Perspective
Mr. Jerry Sachs
FAQ
12/24/2012 Recess
FAQ
12/25/2012 Recess
FAQ
12/31/2012 Recess
FAQ
01/01/2013 Recess
FAQ
01/07/2013 Breakout Session: Mock IRB
Dr. Jerry Menikoff
FAQ
Unit 5:
01/08/2013
FDA Product Regulation
FAQ
Unit 6:
01/14/2013
Institutional Review Boards
Dr. Jerry Menikoff
FAQ
Unit 7:
01/15/2013
Legal Issues in Clinical Research
Ms. Carrie Pottker-Fishel
FAQ
Module 3 - Preparing and Monitoring Clinical Studies
01/21/2013 Federal Holiday
FAQ
Unit 1:
01/22/2013
Information Resources for Clinical Research
Mr. Josh Duberman
FAQ
Unit 2:
01/28/2013
Protocol Development
Dr. Wendy Weber
FAQ
Unit 3:
01/28/2013
Protocol Mechanics and Tools
Mr. Phillip Lightfoot
FAQ
Unit 4:
01/29/2013
Development of Manuals of Operating Procedures
Dr. Wendy Weber
FAQ
Unit 5:
02/04/2013
Pharmaceutical Development: Management of Projects
Dr. Christopher Breder
FAQ
Unit 6:
02/05/2013
Evaluation of a Protocol Budget
Ms. Phyllis Klein
FAQ
Unit 7:
02/11/2013
NIH Peer Review Process
Dr. Valerie Prenger
FAQ
Unit 8:
02/12/2013
Design of Case Report Forms
Ms. Diane St. Germain
FAQ
02/18/2013 Federal Holiday
FAQ
Unit 9:
02/19/2013
Data Management in Clinical Trials
Ms. Diane St. Germain
FAQ
Unit 10:
02/25/2013
Data and Non-Data Aspects of Quality Control in Clinical Studies
Ms. Elizabeth Ness
FAQ
Unit 11:
02/26/2013
Data and Safety Monitoring Committees
Dr. Pamela Shaw
FAQ
Unit 12:
03/04/2013
Technology Transfer
Mr. Bruce Goldstein
FAQ
Module 4 - Miscellaneous Topics
Unit 1:
03/05/2013
Clinical Trial Registries
Dr. Deborah Zarin
FAQ
Unit 2:
03/11/2013
Dissemination and Implementation Research
Dr. Catherine Stoney
FAQ
Unit 3:
03/12/2013
The Clinical Researcher and the Media
Mr. John Burklow
FAQ
Unit 4:
03/18/2013
Health Disparaties Research The handouts for this lecture will not be posted.
FAQ
Unit 5:
03/19/2013
Scientific Conduct
Dr. James L. Gulley
FAQ
Unit 6:
03/19/2013
Community- Based Participatory Research - The handouts for this lecture will not be posted.
FAQ
Unit 7:
03/25/2013
Team Science
FAQ