AACI congratulates the following new members of the AACI Clinical Research Initiative (CRI) Steering Committee. Each will serve a three-year term beginning September 1, 2015:
- Rosemarie Gagliardi, Tisch Cancer Institute, Mount Sinai Medical Center
- Jessica Moehle, BS, CCRP, Huntsman Cancer Institute, University of Utah
- Steve Williamson, MD, University of Kansas Cancer Center
New CRI Steering Committee Members (L-R) Gagliardi, Moehle and Williamson.
The AACI CRI is a network of cancer center clinical research leaders that examines and shares best practices that promote the efficient operation of cancer center clinical research facilities, and leverages the ability of the AACI cancer center network to advocate for improvement in the national clinical trials enterprise.
Rosemarie Gagliardi is Associate Dean of Research Services, Icahn School of Medicine at Mount Sinai; Operations Director, Cancer Clinical Trials Office (CCTO), Tisch Cancer Institute; and Assistant Professor, Department of Population Health Science and Policy. The primary mission of the Tisch Cancer Institute Clinical Protocol and Data Monitoring (CPDM) program is to assist investigators in the development, conduct, and reporting of clinical research in an efficient, compliant and scientifically sound manner. The CPDM provides regulatory, budgeting, study management, compliance, data management and reporting services to ensure clinical research uniformity and consistency. Ms. Gagliardi serves as the CCTO Operations Director, a role established in 2011 to provide direct management of CPDM operations.
Jessica Moehle is Associate Director of Operations, Clinical Trials Office, at Huntsman Cancer Institute. She has more than ten years of clinical research experience, including directing operations for the clinical trials office overseeing a staff of 109 FTEs. Prior to this time she served as the Clinical Trials Regulatory Department Manager and specialized in project management, operational leadership, protocol development, clinical trial portfolio management, IRB regulation, IND submissions, FDA regulation, NCI National Reporting criteria, principal investigator and pharmaceutical sponsor relations, clinical trial staff hiring and training. Ms. Moehle also spent several years in pre-clinical office administration at the National Institutes of Health, Division of AIDS, and Vaccine Research Program.
Stephen Williamson is Medical Director, Clinical Trials Research Unit, and Phase I Director, at University of Kansas Cancer Center. He has been involved in clinical trials research since his oncology fellowship, starting in 1984. Dr. Williamson has been involved in clinical trial development locally and nationally through the Southwest Oncology Group (now known as SWOG). Since 1986 he has been active in the Lung, GI and Head and Neck Committees of the Southwest Oncology Group. His first multi-institutional phase II trial through SWOG was initiated in 1986 and he has been the principal investigator on multiple investigator-initiated trials at the University of Kansas, including a phase I gene therapy clinical trial utilizing irradiated autologous melanoma cells adenovirally transduced with the human GM-CSF gene.