University of Cincinnati Office of Research

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10 search results for Greenphire

Greenphire ClinCard Study Log (XLSX)

This template has been provided by SRS Accounting to help study teams keep track of an individual study’s stock of Greenphire ClinCards

Contact Office: SRS

Modified:

ClinCard Example Letter with Terms (PDF)

ClinCard envelopes should remain sealed and only be opened by the participant receiving the ClinCard. The PDF provides an example of what is contained in the ClinCard envelope.

Contact Office: SRS

Modified:

W-9 (Opens in new window)

Link to the Office of the Treasurer Tax Compliance page in Bearcats Landing.  On this SharePoint page, the study team can scroll down the page to the Form W-9 section.  Within this section, the US payees – Form W-9 section has a link to the current IRS version of the W-9 form.

Contact Office: SRS

Modified:

Genetics Consent (DOCX)

The Genetics Informed Consent Statement is to be used in the following cases:

  1. When the investigator is conducting genetic research on blood or tissue acquired from known subjects (one consent form).
  2. When the investigator is conducting genetic research as a sub-study within another study and the participation in the genetic research is optional (two consent forms for those who participate, one for those who do not).
  3. When the investigator is conducting genetic research as a sub-study within another study, but the participation in the genetic research is not optional, incorporate the additional elements in the genetics consent form into the primary informed consent statement (one consent form).

Contact Office: HRPP

Modified:

Genetics Consent with HIPAA Language (DOCX)

The Genetics Informed Consent Statement is to be used in the following cases:

  1. When the investigator is conducting genetic research on blood or tissue acquired from known subjects (one consent form).
  2. When the investigator is conducting genetic research as a sub-study within another study and the participation in the genetic research is optional (two consent forms for those who participate, one for those who do not).
  3. When the investigator is conducting genetic research as a sub-study within another study, but the participation in the genetic research is not optional, incorporate the additional elements in the genetics consent form into the primary informed consent statement (one consent form).

Contact Office: HRPP

Modified:

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