New Clinical Coordinators Workshop

Sorrell Center, MSC 1005
Omaha, NE

Tuesday, July 15, 2014 @ 8:00 am - 3:30 pm

Training for new clinical research coordinators will be offered during this two day workshop. Topics include informed consent, IRB overview, regulatory documents, contracts, and many more. If you are a new coordinator or know someone who is interested please contact Deb Meyer (9-6941 or dmeyerk@unmc.edu) to register or for further information.

Day 1 Thursday 7/10/2014

8:00 - 8:55 Intro/ Informed Consent - LuAnn Larson, RN, BSN, CCRP
9:05 -10:00 Overview of Clinical Trials - Jen Cavalieri, RN, BSN, CCRC, CCRP
10:00 – 11:00 IRB Overview - Jenny Kucera, MS
11:15-12:00 Handling of Study Medications & Supplies - Jon Beck, PharmD
12:00 – 1:00 Lunch Break
1:00- 1:50 Matrix & Devices - Grace Videtich, BS
2:00- 2:50 Medicare Coverage Analyses - Katie Penas, MHA, CNMT, RT(N)
3:00-3:50 Regulatory Documents/Adverse Events - Sheree Gilmore, BA
4:00- 4:30 Study Feasibility, Using the EHR form - Purnima Guda, PhD


Day 2 Tuesday 7/15/2014
Sorrell 1005

8:00-8:50 Contracts - Deb Vetter, MS
9:00 - 9:40 Organizing Study and Regulatory Start Up: A Coordinators Perspective - Peggy Heires, BA, RD
9:50-10:30 Working with Sponsors/CRO’s Study closure- record storage - Melanie Schrack
10:40 - 11:30 The Recruitment Process for Clinical Trials - Jen Cavalieri, RN, BSN, CCRC, CCRP
11:30-12:00 Research Subject Advocate - Deb Meyer, RN, CCRP
12:00 – 1:00 Lunch Break
1:00-1:40 Site Monitoring - Brigette S. Vaughan MSN, APRN-BC, NP
1:50 - 3:00 Budgeting for Clinical Trials - LuAnn Larson, RN, BSN, CCRP
3:00 - 3:10 Summary and loose ends - LuAnn Larson, RN, BSN, CCRP



Contact Info

Deb Meyer
dmeyerk@unmc.edu
(402) 559-6941

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