The Administrative Office (AO) of the NYUCI plays a crucial role in providing efficient administrative support to the Center Director, Deputy Director, Associate Directors, Core Directors, Program Leaders, and Center Membership. The overall goal is to facilitate research through strategic planning and evaluation initiatives, administration and oversight of core facilities, development of policies and procedures for prudent financial management and grants administration, communications both within the institution and to outside individuals and organizations, human resource management, meetings and seminars, and space and facilities planning. The office is responsible for all interactions with central university finance, sponsored programs, grants management, IRB, Office of Clinical Trials, Human Resources Office, information technology, general accounting and public relations. The AO provides services beyond the activities related to the CCSG such as fiscal management of clinical activities, yet the core mission of the CCSG defines and dictates the structure and decision making processes within the administrative unit. There are eight major areas of focus for research administration: central CCSG administration, grants management, membership, core facilities, structure for inter and intradisciplinary collaborations, research program support, and financial management of the Cancer Institute. Support is requested for only those activities directly related to the CCSG. Since the last review, the administrative office has increased staffing to 17 individuals. This is due in large part to the opening of the Smilow Research Center (3 additional staff to support research administration), faculty recruitment efforts (1 administrative staff), Fellowship Program (one coordinator) and our focus on billing and financial compliance with clinical trials (one financial analyst). There has been significant progress in streamlining financial operations, budgeting, setting fee schedules, invoicing, coordinating research program meetings and seminars, and customizing IT systems for core facilities and clinical trials.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016087-31
Application #
8232198
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2011-03-01
Budget End
2012-02-29
Support Year
31
Fiscal Year
2011
Total Cost
$142,313
Indirect Cost
Name
New York University
Department
Type
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Huang, Chao; Zeng, Xingruo; Jiang, Guosong et al. (2017) XIAP BIR domain suppresses miR-200a expression and subsequently promotes EGFR protein translation and anchorage-independent growth of bladder cancer cell. J Hematol Oncol 10:6
Silvera, Deborah; Ernlund, Amanda; Arju, Rezina et al. (2017) mTORC1 and -2 Coordinate Transcriptional and Translational Reprogramming in Resistance to DNA Damage and Replicative Stress in Breast Cancer Cells. Mol Cell Biol 37:
Koh, Hyunwook; Blaser, Martin J; Li, Huilin (2017) A powerful microbiome-based association test and a microbial taxa discovery framework for comprehensive association mapping. Microbiome 5:45
Ma, Lijie; Liu, Yan; Landry, Nichole K et al. (2017) Point mutation in D8C domain of Tamm-Horsfall protein/uromodulin in transgenic mice causes progressive renal damage and hyperuricemia. PLoS One 12:e0186769
Morabito, Michael V; Ravussin, Yann; Mueller, Bridget R et al. (2017) Weight Perturbation Alters Leptin Signal Transduction in a Region-Specific Manner throughout the Brain. PLoS One 12:e0168226
Koetz-Ploch, Lisa; Hanniford, Douglas; Dolgalev, Igor et al. (2017) MicroRNA-125a promotes resistance to BRAF inhibitors through suppression of the intrinsic apoptotic pathway. Pigment Cell Melanoma Res 30:328-338
Feig, Jessica L; Mediero, Aranzazu; Corciulo, Carmen et al. (2017) The antiviral drug tenofovir, an inhibitor of Pannexin-1-mediated ATP release, prevents liver and skin fibrosis by downregulating adenosine levels in the liver and skin. PLoS One 12:e0188135
Ono, Kentaro; Viet, Chi T; Ye, Yi et al. (2017) Cutaneous pigmentation modulates skin sensitivity via tyrosinase-dependent dopaminergic signalling. Sci Rep 7:9181
Wang, Xing; Zhang, Fenglin; Wu, Xue-Ru (2017) Inhibition of Pyruvate Kinase M2 Markedly Reduces Chemoresistance of Advanced Bladder Cancer to Cisplatin. Sci Rep 7:45983
Garré, Juan Mauricio; Silva, Hernandez Moura; Lafaille, Juan J et al. (2017) CX3CR1+ monocytes modulate learning and learning-dependent dendritic spine remodeling via TNF-?. Nat Med 23:714-722

Showing the most recent 10 out of 1082 publications