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Institutional Review Boards
UM Policies & Procedures - HSRO/IRB
1. Preface
2. Background Topics
3. Authorities and Responsibilities
4. Conflict of Interest
5. Institutional Review Boards
6. IRB Meetings
7. General Principles for IRB Reviews
8. Definition of IRB Review Types
9. IRB Review of Initial Studies
10. IRB Review of Continuing Studies
11. Amendments
12. Closing Studies and Final Reports
13. Suspension, Termination and Administrative Closure of IRB Approved Research
14. Unanticipated Problems and Adverse Events
15. Study Violations
16. Compliance Audits
17. Data Safety Monitoring Boards
18. Ancillary Committees
19. External IRB's
20. Policies Specific to Certain Types of Research
21. Informed Consent
22. Participant Recruitment Methods, Advertising Materials and Recruitment-Relevant Payment Arrangements
23. Vulnerable Populations
24. Privacy, Security, Confidentiality and HIPAA
25. Subcontracts/Agreements for UM-Initiated Studies that Engage or Involve non-UM Institutions or Investigators
26. International Research
27. Emergency Use
28. Record Retention
Other Policies
UChart Forms & Guidance
HSRO Forms & Documents
University Fees
Ancillary Committee Information
eProst User Guide
Ethics, Federal Regulations & Guidance
HIPAA
Translations
Western IRB (WIRB)
About the HSRO


Basic Folder Information

3.5 Responsibilities of UM Deans/Department Chairs


Approval Date

 

Review Responsibility:

IRB Policy and Procedure Committee

Original Approval Date:

December 19, 2006

Revised: May 10, 2011; June 8, 2011

 



3.5 Responsibilities of UM Deans/Department Chairs

It is the responsibility of the academic department chairperson (or Dean in a non-departmentalized School of the University) and other University officials (such as Center Directors for studies being conducted within the facilities or with support from that Center) to assist in ensuring that IRB determinations are followed.  Submission of a study or study amendments for IRB approval shall require that these persons or their designees grant permission for that submission via ePROST (electronic signature) noting that he/she certifies that the research study referenced in the study application or amendment is well designed and scientifically sound. This permission shall also be confirmation that appropriate financial and other necessary resources are available, that the credentials of all persons engaged in the research appropriate and that investigators have sufficient time to carry out their study commitments and oversee conduct of the research.

It is also the responsibility of the academic department chairperson (or Dean in a non-departmentalized School of the University) to inform the IRB of situations that may preclude a Principal Investigator from continuing in his/her role as Principal Investigator and to recommend to the IRB any changes of Principal Investigator for ongoing studies in which the original Principal Investigator is either unwilling or unable to continue in this position.



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