- Human Research Professionals Monthly Meeting
This monthly program focuses on educating research faculty and staff on current research processes or new developments within MCW and Froedtert. The presentation is generally held on the last Tuesday of the month. Attendees are welcome to bring their lunch. A beverage and dessert are provided.
Please visit Past Meeting Presentations for some of our past meeting presentations.
Beginning January 2014 registration for this and all other Human Research Protection Grand Rounds course presentations must be filed in EthosCE.
If you previously created your EthosCE profile and registered for the Human Research Protection Grand Rounds course no additional registration is necessary.
If you have not created your EthosCE profile or registered for the Human Research Protection Grand Rounds course in EthosCE please create your EthosCE profile now and register for the Human Research Protection Grand Rounds course.
Next Human Research Professionals Meeting
September 30, 2014
MCW HRC H 1210-1230
11:30 a.m. - Noon: Announcements & Seating
Noon - 1:00 p.m.: Program
Safety Committees: Essential Partners in Research
MRI Safety, Institutional Biosafety, Hazardous Chemicals, Radiation Safety, Occupational Health
L. William Cashdollar, PhD: Director, Core Laboratories at Blood Research Institute; Adjunct Associate Professor, Microbiology and Molecular Genetics at MCW; Interim Biological Safety Officer at MCW
John Krezoski, PhD: Chair, Hazardous Chemicals Safety Committee
Christopher Mol, RN, BSN, MBA, COHN-S: Clinic Manager, Froedtert & MCW Occupational Health and International Travel
Julie Peay, BSM RT(R)(MR), FSMRT: MRI Program Manager
Jason Timm, MPH: Assistant Radiation Safety Officer
Learn what activities need Safety Committee review
Understand the importance of Safety Committees
Increase awareness of how research activities affect subjects, researchers and healthcare workers
Questions? Send an e-mail to Connie Byrne.
Everyone interested in the review or conduct of research is welcome.
The Medical College of Wisconsin is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. Program ID: 14075
Designation of Credit Statement
The Medical College of Wisconsin designates this live activity for a maximum of 1.5 AMA PRA Category 1 CreditTM. Physicians should claim credit commensurate with the extent of their participation in the activity.
Hours of Participation for Allied Health Professionals
The Medical College of Wisconsin designates this activity for up to 1.5 contact hour of continuing education for allied health professionals.
Psychology CE Credit Statement
The Medical College of Wisconsin is approved by the American Psychological Association to sponsor continuing education for psychologists. The Medical College of Wisconsin maintains responsibility for this program and its content. This activity contains content or processes that may be potentially stressful.
Upcoming Human Research Professionals Meeting
Date: November 25, 2014
- Human Research Series Modules A, B and C
The Human Research Series is intended for MCW employees whose job responsibilities include any aspect of human research, are optional modules that can be taken in any order. Individuals are welcome to choose which modules to attend, according to their job needs.
There are currently three modules held quarterly on a rotating monthly basis, lasting 90 minutes each:
Module A - IRB Processes
Module B - Research Banks at MCW & Froedtert Hospital
Module C - Conducting Human Research at Froedtert Hospital: What You Need to Know
Sessions are typically small in size, allowing time for questions, interaction and networking.
View more information on our Human Research Series here
- MCW Certification Program (CITI)
In 2004 MCW announced the requirement to all individuals involved in the design, conduct or review of human subjects research to have been certified under a new educational program. The program requirements include reading the Belmont Report and key MCW research documents and policies, completing the required modules of the Collaborative IRB Training Initiative (CITI) Program, maintaining CITI certification and additional annual educational requirements.
View more MCW Certification Program (CITI) information
- Core Education: Boot Camp
The purpose of this educational event is to provide resources to the human research team member in the coordinator role that will expedite his/her ability to perform his/her job responsibilities in a manner consistent with federal requirements and guidance and other applicable policy. The focus of this course is the very basic day to day functions of conducting research with an emphasis on providing practical information and tools that can be used immediately.
Human Research Team members including: Clinical Research Coordinators, Clinical Research Assistants, Research Nurses, and other individuals responsible for the conduct of human research protocols. Course content is geared toward those with limited experience in their roles. Experienced human research team members seeking to broaden their knowledge base and acquire additional human research management skills are welcome.
View more information on Core Education: Boot Camp here
- IRB Lunch & Learn
The IRB Lunch & Learn meetings are generally held on the third Tuesday of every month, from 12:00pm - 1:00pm in the MACC Fund building meeting room 3075.
Several IRB staff members will be available on a walk-in basis to help you with the IRB review process. The first 20 minutes will be devoted to brief presentations on issues of general interest; the remaining 40 minutes is your time for questions and direct assistance.
- IRB Frequently Asked Questions
Visit our IRB FAQ page for an archive of questions that have been answered for investigators and study teams. Topics included HIPAA, FWA, Exempt projects, Informed Consent, etc.
- Informed Consent Frequently Asked Questions
Visit our Quality Improvement Program FAQ page for an archive of questions that have been answered for investigators and study teams on the subject of informed consent.