Office of Research Events & Workshops

  • March 21, 2019 1:00 PM
    The OnCore Central Support Team provides support and training to help the clinical trials community transition to OnCore. Each OnCore training session provides hands-on training that allows staff and...
  • March 22, 2019 3:00 PM
    This course offers guidance on writing informed consent documents. Discussion will explore strategies for creating documents that are easy to read, easy to understand, and compliant with federal and...
  • March 26, 2019 9:00 AM
    This course will review the application types in eResearch for research that is not regulated; research that is limited to secondary research, and for those projects lacking immediate plans for...
  • April 1, 2019 11:30 AM
    Are you interested in clinical trials research, but don’t know where to start? Are you eager to learn best practices from your colleagues?
  • April 2, 2019 9:00 AM
    This course will review the FDA requirements for conducting research with a drug or medical device, including conducting research under an IND (Investigational New Drug Application) and an IDE (...
  • April 3, 2019 8:00 AM
    Offered by the Office of Faculty Affairs & Faculty Development, this workshop covers writing grant proposals for all types of grants, including NIH, NSF, and foundations.
  • April 9, 2019 1:00 PM
    The OnCore Central Support Team provides support and training to help the clinical trials community transition to OnCore. Each OnCore training session provides hands-on training that allows staff and...
  • April 12, 2019 9:00 AM
    This course will examine the additional regulatory requirements for conducting research involving children, pregnant women, fetuses, neonates, and prisoners. The course will include the requirements...
  • April 16, 2019 5:00 PM
    Are you interested in partnering with industry on a clinical trial, but are unsure of where to start? Have you been hesitant to pursue an industry trial because you’re not sure who can help here at U...
  • April 19, 2019 9:00 AM
    This course will identify what constitutes an Adverse Event, ORIO, and Unanticipated Problem and review the requirements of reporting such events to the IRB via eResearch. This session will also...

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