ThINK Series Past Seminar Materials

2006-2007 Seminars

Subject Recruitment and Retention: Strategies that Work - Part 2 of 2

• Seminar Materials: Brenda Montogmery, R.N.,
  Department of Medicine, Diabetes Research Group, VA Puget Sound Health Care System
• Seminar Materials: Margaret Neff, M.D.,
  Assistant Professor, Department of Medicine Division of Pulmonary & Critical Care,
  Harborview Medical Center

Subject Recruitment and Retention: Strategies that Work- Part 1 of 2

• Seminar Materials: Donna Edgerton, BSN, RN, CCRC
  Director, Clinical Operations
  Sonus Pharmaceuticals,
  Bothell, WA
• Seminar Materials: Jan Englund, MD
  Associate Professor, Pediatrics, Division of Immunology/Rheumatology
  Division of Immunology/Rheumatology,
  Children's Hospital & Regional Medical Center

Why I Participate in Research: From a Research Subject's Perspective

• Anthony L. Back, M.D., Division of Medical Oncology, University of Washington

Clinical Research - Working with the Media

• Seminar Materials: Tina Mankowski, Director, Health Sciences/UW Medicine News and Community Relations

The Changing UW Climate for Clinical Research: Town Forum

• Seminar Materials: Nora Disis, M.D., Director, UW General Clinical Research Center, Principal Investigator, Clinical and Translational Science Award
• Seminar Materials: Jeffrey M. Cheek, Ph.D., Associate Vice Provost for Research, Compliance and Operations, UW Office of Research; Karen Moe, Ph.D., Acting Director of the Human Subjects Division, Research Associate Professor, UW Department of Psychiatry and Behavioral Sciences
• Seminar Materials: Richard J. Meisinger, Jr.. Ph.D., Assistant Dean for Planning and New Initiatives, Office of Research and Graduate Education, UW School of Medicine
  
  

2005-2006 Seminars

Conducting Investigator Initiated Protocols: Points to Consider

• Seminar Materials: Victoria (Tory) Lake, RAC, Regulatory Affairs Director,  Fred Hutchinson Cancer Research Center
• Seminar Materials: Lupe G. Salazar, M.D., Department of Medicine, Division of Oncology, UW School of Medicine

 

How to Stay Out of Trouble - Compliance at UW Medicine: What it is and What it Should Be

• Seminar Materials: John Slattery, PhD, Vice Dean for Research and Graduate Education, UW School of Medicine

Potential and Real Conflicts of Interest in Clinical Research

• Seminar Materials: Malcom Parks, Ph.D., Associate Vice Provost for Research, Michael Corn, J.D., Director of Industry Relations, School of Medicine

The UW and Western Institutional Review Board: "Working with WIRB - Nuts and Bolts"

• Seminar Materials: Helen McGough, MA, CIP, Director, Human Subjects Division, Office of Sponsored Programs
• Seminar Materials: David Forster, JD, MA, CIP, Director, Regulatory Affairs, Western Institutional Revew Board

2004-2005 Seminars

Financial Considerations in Clinical Research

• Seminar Materials: Laurie M. Whitney, Acting Director, Clinical Research Budget and Billing Support Office (CRBB), UWMedicine 
  

Downstream Implications of Tissue Banking Consent, HIPAA, IRB - Lots of Rules to Consider

• Seminar Materials: Shelly Heimfeld, PhD, Associate Member, Clinical Research Division, Fred Hutchinson Cancer Research Center 
  

Records-based Research: 
* With Institutional Medical Records
* With Your Own Clinical Database

• Seminar Materials: Harold Goldberg, MD, Professor of Medicine, and Pam Shoberg, Program Manager, Consolidated Decision Support, UW Medicine IT Services, Kris Kowdley, MD, Professor of Medicine

Ten Top Problems that IRBs See in Applications (That Might Suprise You)

• Seminar Materials: Zane Brown, MD, Chair, Human Subjects Review Committee A and Helen McGough, Director, Human Subjects Division

Surviving the Responsibilities of a Clinical Investigator

• Seminar Materials: Nora Disis, MD, Program Director, UW General Clinical Research Center

2003-2004 Seminars

To obtain copies of slides from the 2003-2004 ThINK Series, please send an email message to: gstreidl@u.washington.edu

Legal Issues Associated with Conducting Clinical Trials - What You Need to Know

• Suzanne Page, JD, Director of Industry Agreements, Grant and Contract Services
  

Successfully Navigating the UW Review Process

• Helen McGough, MS, Director, Human Subjects Division
  Rick Hudson, PhD, Radiation Safety Committee
  David Emery, PhD, Institutional Biosafety Committee
  Bill Anton, Implant and Investigational Device Committee
  Sheree Miller, PharmD, Investigational Drug Services, UWMC
  Marc Provence, FHCRC/UW Cancer Consortium
  John Brunzell, General Clinical
  Research Center
  

FDA Perspectives on Research in Academic Medical Centers

• Donna Edgerton, RN, BSN, CCRC, Director, Clinical Quality Assurance, Corixa Corporation