New Jersey Dental School - Office of Research

Dr. Michael L. Barnett, Interim Associate Dean for Research
Ms. Latona Thompson, Management Assistant
The Office of Research provides administrative support for all research activities of the New Jersey Dental School. It promotes and coordinates research programs and assists faculty in identifying external funding sources and in preparing and submitting grant applications. It is also responsible for ensuring that all grant applications and contracts comply with federal, state, University, and sponsor requirements. Accordingly, this office reviews grant applications and provides final signature authorization that all such requirements have been satisfied.
The Office of Research also sponsors student research through its administration of the Student Research Group and organization of the Student Summer Research Program. A limited number of summer research fellowships are available to students through this office every year.
Please use the links on this page to obtain preliminary information on preparing and submitting grant applications. Further assistance is available from this office.
Office of Research
New Jersey Dental School
Room D741
110 Bergen Street
Newark, New Jersey 01701-1709
Clinical Research Group:
The mission of the Clinical Research Group (CRG) is to facilitate and coordinate clinical research at the UMDNJ-New Jersey Medical School and other schools on the Newark campus of UMDNJ. This service supports investigators conducting clinical and translational research, provides interested business partners centralized access to University investigators, educates research subjects about clinical trials at UMDNJ, in-services clinical staff and investigators about Good Clinical Practices guidelines, and delivers legal and fiscal oversight.
The New Jersey Medical School - Clinical Research Group is a resource available for the planning, implementation, management, monitoring and reporting of clinical research and activities conducted at the Newark campus of UMDNJ. These tasks are not only scientific in nature, but can also be administrative, fiscal and regulatory. The CRG will integrate and centralize data collection, management and regulatory procedures from all participating clinical trials and clinical protocols, observational studies and translational research being conducted with participating investigators.