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School of Medicine

Past Workshops for Researchers


2006


National Council University Research Administrators (NCURA) 2006 Video Workshop

KU Medical Center Research Institute will be sponsoring this year’s NCURA 2006 Video Workshop; this is the first of four in the series.

Post-award Issues for the Pre-award and Departmental Administrator
KUMC, January 24, 2006
Wahl West Auditorium
10:30 AM - 2:30 PM

Learning Objectives:

  • Participants will gain a greater awareness of the impact that both pre-award and post-award functions have on each other.
  • Participants will understand the impact that decisions made in the proposal and award negotiation stage have on the PI, and the institution's ability to conform with the terms and conditions of the award
  • Departmental Administrators (the advocate for the PI) will have a better understanding of what the pre-award administrator needs are and the pre-award administrator will have a better understanding of what the post-award administrator needs are regardless of the size of the institution or the number of FTE devoted to research administration.

Moderator: Ed Herran, Director, Office of Sponsored Projects, Memorial Sloan-Kettering Cancer Center

Faculty: Marilyn Surbey, Associate Vice President for Finance and Research, Emory University; Toni Lawson, Associate Director, Office of Research Administration and Advancement, University of Maryland, College Park; Patrick Fitzgerald, Director, Office of Sponsored Programs, Massachusetts Institute of Technology

For additional information view web link: http://www.ncura.edu/conferences/videoseries/2006/schedule.htm

GRANTS.GOV: Working towards a common vision

March 7, 2006
KUMC School of Nursing
room 1050
10:30 AM - 2:30 PM

Contact Kelly Robertson at (913) 588-5436, krobertson@kumc.edu, at KU Medical Center Research Institute to RSVP, ask questions, or for directions.


2005


Biological Safety Cabinets and Fume Hoods Training

Attention KUMC Researchers and Staff. You are invited to "Biological Safety Cabinets and Fume Hoods 101". The first presentation in the Laboratory Safety Brown Bag series sponsored by the Safety Office. Presented by Senior Sales Representative Scott Ward, Labconco.

Date: September 7, 2005 from 12:30 - 1:30 pm at 1023 Orr Major. Feel free to bring your lunch. Snacks will be provided.

New Clinical Study Website Registration Requirements: International Conference of Medical Journal Editors Policy Review

Presenter: Laurie Kemble, BHS, CRT Director, Clinical Research Administration KUMC Research Institute, Inc.
Time: 12 noon - 1 pm
When: September 15, 2005
Where: Wahl Hall East Auditorium

Research Orientation

September 22, 2005
10 a.m. - Noon
Lied Auditorium
Please RSVP for head count

Faculty, study coordinators and research administrative personnel are encouraged to attend the 2 hour overview on conducting research at KUMC. Topics to be addressed include: organization & services of the Office of Compliance, the KUMC Research Institute, research committees (such as: Human Subjects, IACUC, Safety committees), human resources/equal opportunity, legal issues and more. This session is intended to be a high level overview to introduce faculty/staff to the areas with which they will interact as research personnel. This is also an opportunity to ask questions to help determine future educational topics.

If you would like to attend, but cannot make it to this session, another session will take place from 1-3 p.m. on Oct. 4.

2004


"Effort Reporting: In Principle & In Practice"

Thursday, September 23, 2004
11:30 a.m. - 1:00 p.m.
Clendening Auditorium

Presenters:
Bruce Elliott, Director, Chicago Campus, Office of Sponsored Research, Northwestern University
Jennifer Hubert, Project Manager, Effort Report, Northwestern University

"General Responsibilities of the Sponsor, Investigator, and Study Coordinator"

Thursday, October 21, 2004
12pm - 1pm
Wahl Hall East Auditorium

"General Responsibilities of the Human Subjects Committee (HSC), Food and Drug Administration (FDA), and Office of Human Research Protections (OHRP)"

Presenter: John R. Finley, JD, MPH
Associate Vice Chancellor for Compliance, KUMC

Tuesday, November 16, 2004
12pm - 1pm
Wahl Hall West Auditorium

"Investigator-Initiated research: Pearls and wisdom from both sides of proposal"

Presenter: Tom Peddicord, PharmD, FCCP
Regional Scientific Associate Director, Respiratory/Dermatology, Novartis Pharmaceuticals

Thursday, December 16, 2004
12pm - 1pm
Clendening Auditorium

2003


KUMC Research Faculty and Staff Orientation

September 18, 2003
Lied Auditorium
10:00 a.m. - 12:00 noon

September 30, 2003
Clendening Auditorium
1:00 p.m. - 3:00 p.m.

Both sessions will cover the same content. KUMC Research Personnel are encouraged to attend one of the two sessions. See the Research Compliance web site for more information.

"Clinical Study Development Process"

Clinical Trials Educational Lecture Series
Thursday, September 16th
12:00 p.m. - 1:00 p.m.
Wahl Hall West Auditorium

"Informed Consent Requirements: What Researchers Can and Can't Do in Reusing Research Data and Human Biologic Materials"

Monday, August 2, 2003
Wahl Hall East
4:00 p.m. - 5:00 p.m.
Presenter: Mark Barnes, J.D.

Video tapes and, in some cases, handouts are available for the following 2002/2003 sessions:

How Do You Know if They are doing Research on You, when can You do Research on Them? An Insider’s View of IRBs and Human Subjects Review: March 16, 2003

Jerry Menikoff, JD, MD, Associate Professor of History and Philosophy of Medicine and Ophthalmology Chair, KUMC Human Subjects Committee.

Video tapes are available for check-out.