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Clinical Research Update (CRU) Series:
This series consists of eight brown-bag workshops on
various clinical research topics. The target audience
includes research coordinators, staff, and investigators
directly involved in conducting clinical trials. These
programs are designed to keep staff updated on |
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good clinical practice guidelines, present tools and
resources for successful clinical trial management, and provide
opportunities for networking and team building. Presenters include
both University staff members and outside speakers, both recognized for
their expertise in the topic areas.
Continuing Nursing Education credit is provided for the programs
via the College of Nursing.
Because the series is accredited, the Association of Clinical Research
Professionals (ACRP) and Society for Clinical Research Associates (SoCRA)
accepts these programs for certification maintenance.
For more information on the CRU
series or to be added to the brochure mailing list, contact Ryan Vicini at
(859) 323-8545 or
rlvici2@uky.edu.
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Clinical Research Updates
2007-2008 |
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Date
Lunch
@11:30am
Presentation @ noon |
Location |
Topic/Title |
Speaker(s) |
Thursday
August 30 |
MN463 |
(rescheduled from
March 07)
Human Research Protection Update (post AAHRPP) |
Ada Sue Selwitz,
MA
Director, Office of Research Integrity & Adjunct Associate
Professor, Behavioral Science
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Wednesday
Sept 12 |
MN
363
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Clinical
Trial Agreements |
Deborah
Davis
Director, Office of Sponsored Projects Administration |
|
Thursday
Oct. 18 |
HG611
|
Bench to Bedside: Using Lean Techniques to Get From the Clinical Research Bench to the Bedside
|
Paul DePriest, MD
Professor, OBGYN
Jeff Norton, M.S.
, Co-Director, Center for Quality, Safety, & Patient Rights |
Thursday
Nov 15 |
HG611
|
Designing Smarter
Clinical Trials |
Richard
Kryscio, PhD
Associate
Professor, Dept. of Statistics, College of Arts & Sciences
Chair,
Department of Biostatistices, College of Public Health
Director,
CCTS Biostatistics, Design & Research Ethics |
Thursday
Dec 20 |
HG611
|
Global Drug
Development: The Shape of Things to Come |
Thomas S. Foster,
Pharm.D
Professor of Pharmacy, UK College of Pharmacy & Associate Professor
of Anesthesiology, UK College of Medicine |
Thursday
Jan 17 |
HG611
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Practice-Based Research and the Community |
Kevin Pearce,
MD
Professor & Vice Chair, Academic Affairs and Mary Barron, RN
Sr. Research Nurse Coordinator Family & Community Medicine and
Kentucky Ambulatory Network |
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Thursday,
February 21
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Medicare Coverage Analysis for Clinical Research
Trials |
Rebecca Scott
Clinical Research Compliance Manager
Office of Corporate Compliance
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Thursday
March 20 |
HG611 |
Conflict of Interest |
Deborah
Davis
Director, Office of
Sponsored Projects Administration (OSPA)
Carole Cole
Conflict of Interest Administrator, OSPA |
Thursday
April 17 |
HG611
|
Best Practices in Research Documentation |
Linda Rice,
RN, CCRC
Director of
Operations
CR-DOC/GCRC
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Presentation
Archives- UKCRO/GCRC Clinical Research Updates
2006-2007 |
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Date
Lunch
@11:30am
Presentation @ noon |
Location |
Speaker(s) |
Topic/Title |
| September
20, 2006 |
MN263 |
Joe Kaufman
Quality Assurance Director
Community Research Cincinnati |
Anatomy of a
Good Clinical Study |
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October 18, 2006 |
HG611 |
Ellen Hahn, DNS, RN
Professor, UK College of Nursing and Public Health
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Smoke-free Policy Research: Translating Outcomes Research into
Practice |
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November 8,
2006 |
HG611 |
John Steiner, JD Corporate Compliance Officer |
Clinical Research Compliance -
Overview |
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December 13, 2006 |
HG611 |
Andrew Bernard, MD Assistant Professor
UK General Surgery |
You want to do
what?!!
Using the FDA's Provisions for Exception from Informed Consent at
Study Enrollment - The PolyHeme Ambulance Trial as a Model |
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January 17, 2007 |
PH223 |
Thomas S. Foster, Pharm.D. FCCP, FCP, FAPHA Professor
and Executive Chairman , Medical IRB, Colleges of Pharmacy and
Medicine |
Promising Translations
in Drug Development: A Global Perspective |
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March 21, 2007 |
TBN |
Ada Sue
Selwitz, M.A. Director, Office of Research Integrity
Adjunct
Associate Professor, Behavioral Science |
IRB
Update – Post Accreditation
POSTPONED until fall of 2007
TBA |
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April 18, 2007 |
PH223 |
Jody L. Clasey, Ph.D., FACSM,
Associate Professor, Department of Kinesiology and Health Promotion |
The GCRC
Functional Assessment and Body Composition Core: Research, Requests,
and Resources |
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May 16, 2007 |
PH223 |
Jo A. Hudson, R.N., Administrative
Coordinator, and Alise Brickhouse, C.R.A., Sanders-Brown Center on
Aging - Cultural Outreach in Dementia Services
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Cultural Outreach in Dementia Services |
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August 30, 2007 |
MN 463 |
Ada Sue
Selwitz, M.A. Director, Office of Research Integrity
Adjunct
Associate Professor, Behavioral Science |
Human Research
Protection Update |
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Presentation Archives 2005-2006:
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| Date |
Room |
Speaker(s) |
Topic |
CEU |
| Sept. 21, 2005 |
MN263 |
Vince Cecil, RSN, BSN, Director
of Patient Care Services GCRC |
Guidelines for using
the General Clinical Research Center |
1 |
| Oct. 19, 2005 |
MN263 |
C. William Balke, MD, FACP,
Senior Associate Dean for Research, Director of the Institute of
Molecular
Medicine, Professor of Medicine and Physiology |
"The Yellow Brick
Road[map]":
The Future of Clinical & Translational Research at UK |
1 |
| Nov. 9, 2005 |
UK Auditorium
HG611 |
John Thompson, MD, Chair, VA
Research & Development |
VA R&D - Streamlining
the application process |
1 |
| Dec. 14, 2005 |
MN363 |
Don Keach, Division Manager,
Intellectual Property
Tom Goodness, Division Assistant Director, Intellectual Property |
Intellectual
Property at UK |
1 |
| Jan. 18, 2006 |
UK Auditorium
HG611 |
John Novak, BDS, LDS, MS, PhD,
Professor and Associate Director Center for Oral Research |
The NIH Roadmap: The
Future of Clinical Research Growth and Success at UK" |
1 |
| March 22, 2006 |
MN463 |
Marietta Watts, Training
Specialist, UK Department of Human Resources and Dawn Dawson,
Study Coordinator, Center for Oral Health, UK College of
Dentistry |
Multicultural
Research Recruitment |
1 |
| April 19, 2006 |
UK Auditorium
HG611 |
Ada Sue Selwitz, MS, Director, UK
Office of Research Integrity, Member of the Secretary's Advisory
Committee on Human Research Protections (SACHRP) Subpart A
Subcommittee |
Human Research
Protection Program Update |
1 |
| May 17, 2006 |
MN463 |
M. Sara Rosenthal, PhD, Director, University
of Kentucky Program for Bioethics and Patients' Rights,
Assistant Professor, Bioethics Department of Behavioral Science |
Ethical Dilemmas in Clinical
Research: Resolving Clinical Uncertainty |
1 |
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2004-2005: |
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Date
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Room
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Speaker(s)
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Topic
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CEU
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Sept. 15, 2004 |
MN463 |
Joe Kaufman, B.S.
(former FDA Inspector) Community Research, Cincinnati, OH |
The Anatomy of an FDA Study-Oriented
Inspection |
1 |
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Oct. 20, 2004 |
MN463 |
Judi Kuhl,
Office Research Integrity |
Human Subjects Quality Improvement
Self-Assessment |
1 |
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Nov. 17, 2004 |
MN363 |
Elaine Yonce - Medicare, Lorra
Miracle, RN - IUT Submission/Approval,
Tom Foster
FDA Approval Process |
Special Considerations for Device Trials Device Advice - 1.5
to 2 hr. program |
1-2 |
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Dec. 8, 2004 |
NURS 201 |
Deborah Davis, Office of Sponsored
Projects Administration,
Ada Sue Selwitz, Office of Research Integrity |
Conflict of Interest in Human Research Studies: OHRP Guidance |
1 |
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Jan. 19, 2005 |
NURS 201 |
Stephen J. Anderson
Regina M. Heiser
Brett S. Rowlet
ICIS Project Members |
The ICIS Medical Record System |
1 |
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March 23, 2005 |
NURS 201 |
Judi Kuhl,
Office Research Integrity |
Mission Possible: Improvements to IRB Applications
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1 |
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April 20, 2005 |
NURS 201 |
Fred Schmidtt, M.D. Center on Aging |
Subject recruitment in an aging populations:
Lessons & Experiences
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1 |
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May 18, 2005 |
NURS 115 |
Jim Hilvers, Security Officer
Brett Short, Privacy Officer |
Technology and Security
in a Clinical Research Environment
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1 |
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Comments
to Roxane
Poskin, Last Modified:
April 23, 2008
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