Study Coordination Services

The Office of Clinical Investigative Services provides:

• Single contact point for investigators, clinical research staff, and corporate sponsors.
  
  
• Clearinghouse for current and potential clinical research projects
  
  
• Tracking of each clinical research project through the approval process
  
  
• Negotiated fixed charges for laboratory processing and other research support services
  
  
• Liaison services between investigators and other MCG offices that work with clinical research
  
  
• Host of Study Manager, a web-based application that financially and programmatically manages clinical studies. (For more information, see the Study Manager web page)
  
  
• Patient screening and recruitment
  
  
• Study coordination
  
  
• Patient visit and procedure scheduling
  
  
• Licensed staff to conduct procedures and monitor patient health
  
  
• Financial management of study accounts
  
  
• Case Report Form completion
  
  
• Clinical trial regulatory material preparation and maintenance
  
  
• Space and equipment to conduct research

       Quality Assurance

• All studies conducted in accordance with the Code of Federal Regulations, Good Clinical Practices, and the Health Insurance Portability and Accountability Act, and institutional policies
  
  
• Standard Operating Procedures
  
  
• Internal audits conducted by the Office of Human Research Protection

      Experienced Research Staff

• Licensed Medical Director:
  Anthony L. Mulloy, Ph.D., D.O.
   
• Licensed Operations Manager:
  Kathy Miles, NHA, BS, C.R.C.P.
  

• Regulatory Manager:
  Barbara Covington

• Business Manager:
  Elise Moradi, BBA

• OCIS Outpatient Clinic Coordinators:
  Kay Bailey, RN, BSN, CCRC

Latanya Bowman, RN, BSN
Kilwanna (Kiki) Bush-Brown, RN, BS

Nancy Flippin, RN, BSN
Maria Powell, LPN, CCRC
Kate Sideman, RN, BSN
Charlene Weathers, RN, BSN, CNN, CCRC
 

• OCIS Outpatient Research Staff:
  Shana Kay Seamans, BS
  Maria Swires