Research Team Member Guidebook


Section I
Human Subjects and/or Human Derived Materials
1 Office of Clinical Investigative Services (OCIS)
2 Coordinator Responsibilities
3 Human Assurance Committee (HAC)
4 Industry Sponsored Clinical Research Pathway
5 Institutional Review Board (IRB) - See Human Assurance Committee
6 Investigator's Responsibilities
7 MCG Legal Office
8 Miscellaneous
9 Monitoring Visits
9a Study Sponsors and Site Visits
10 Office of Human Research Protection
11 Records Management
12 RESCUE
13 Surgical Research Services

Section II
MCGHI Policies
1 Health Information Management Services (Medical Records)
2 Hospital Financial Management
3 Investigational Pharmacy/Clinical Research Pharmacy
4 Patient Accounting

Section III
Financial
1 Comptroller's Division
2 Medical College of Georgia Research Institute (MCGRI)
3 Sponsored Program Administration
4 Physicians Practice Group (PPG)
5 Supply Administration

Section IV
Laboratory Information
1 Off-Site Service Providers
2 Pathology

Section V
Professional Societies
1 Association of Clinical Research Professional (ACRP)
2 Drug Information Association
3 Society for Clinical Research Associates

Section VI
Veterans Affairs Medical Center (VAMC)
1 VAMC R&D Committee
2 Augusta Biomedical Research Corporation (ABRC) Contracts

Section VII
Miscellaneous Information
1 Consultant Agreements
2 Dry Ice
   

 

 

If you have any questions about these templates, please contact Crystal Hucksam, chucksam@mcg.edu, 721-3110, Sharon Willing, swilling@mcg.edu, 721-1482; or Lynnette Butler, lybutler@mcg.edu, 721-8397.

 

 

 

 

Revised September 16, 2008.   Please send comments, suggestions or questions about this page to Angela Randazzo, ohrp@mcg.edu.