ADCS Staff

Administration Core

Jackie Bochenek, Director of Clinical Trials Administration – Directs and coordinates management activities of the ADCS Coordinating Center.

Peggy Chambers, Recruitment Specialist – Oversees recruitment and retention plans for protocols, serves as a central resource for study recruitment strategies, maintains library of general recruitment, minority recruitment, and retention collaterals in addition to caregiver materials.

Jeffree Itrich, ADCS Communications Specialist – Supervises concept and implementation of protocol specific recruitment and retention for each ADCS clinical trial, develops study communications plans, writes press releases/conducts study public relations campaigns, and manages the ADCS website group.

Dave Lamb, Financial Assistant – Processes clinical trial site payments and facilitates ADCS-related travel expenses.

Jeremy Pizzola, Senior Fund Manager - Responsible for providing fiscal oversight of ADCS funds including grant awards, gifts, contracts, subcontracts, clinical trial payments, and other financial matters of the ADCS.

Mayca Roig, MS, MA, MBA, Programmer/Analyst – Responsible for design, development, maintenance, and support of some computer software systems serving for ADCS Coordinating Center, such as the clinical trial electronic site payment systems and financial projections.

Elizabeth Shaffer, Regulatory Affairs Assistant & Events Coordinator – Provides support of regulatory compliance; responsible for coordinating and planning ADCS and ADNI Steering Committee Meetings and Protocol Training meetings.

Debbie Stice, ADCS Contracts Coordinator & Events Manager - Serves as a liaison with ADCS clinical trial sites; responsible for initiating site contracts and management of protocol specific site contracts; Oversees coordinating and planning of ADCS Steering Committee Meetings.

Deborah Tobias, Fiscal Operations Manager – Responsible for the overall daily management and leadership for the administrative and fiscal activities of the ADCS.

Kristin Woods, Regulatory Affairs Coordinator – Responsible for providing management and oversight of regulatory compliance for ADCS clinical trial studies; assists with protocol development and works with the Project Directors; creates, reviews and assesses research material that is submitted to regulatory agencies, affiliated institutions and their Institutional Review Boards (IRB); oversees and collects Conflict of Interest reports for all members of the ADCS.

Baoyuan Zhao, Manager of Information Technology and Software Development – Responsible for overall planning, organizing, and execution of IT functions for the ADCS Coordinating Center, including directing IT operations, as well as the support and maintenance of existing IT infrastructure and development of new technical solutions. Also responsible for planning, design and developing and implementing complex computer software systems serving for ADCS Coordinating Center.

Clinical Operations

Devon Gessert, Manager, Clinical Operations – Directs and coordinates all of the activities within the Clinical Operations Group.

Karen Stokes, Project Coordinator

Sarah Walter, Project Coordinator

Barbara Bartocci, Project Coordinator

ADCS Project Coordinators work directly with investigators and other groups within the ADCS to coordinate all aspects of ADCS studies, from protocol development to implementation, startup, maintenance, and close-out and serve as the primary point of contact for questions that arise regarding study procedures.

Larry Janus, ADCS Publications Coordinator ADCS Publications Coordinator – Responsible for design, customization and production of ADCS publications including study related materials such as recruitment materials, procedures manuals, and newsletters.

Brandon Stanley, Shipping and Inventory Specialist – Manages and ships study supplies for all studies, serves as main point of contact for site contact information updates.

Traves Butterworth, Office Manager – Provides general administrative support, including fielding calls from sites, responsible for certifying ADAS raters.

Data Core

Ron Thomas, Director, Data Core

Rema Raman, Associate Director, Data Core

Gustavo Jimenez, Director, Informatics

Shelia Jin, Statistics

Lisa Simon, Quality Assurance

Medical Operations

Adam S. Fleisher, M.D., Medical Director. Handles oversight of clinical trial safety monitoring and reporting.

Michael Rafii, M.D., Ph.D, Associate Medical Director. Supervision of medical safety coding and liason with site clinicians regarding medical inquiries.

Kim Hyun, Ed.D., Medical Analyst. Reviews and analyzes safety-related laboratory, medication and protocol reports, generates reports for Data Safety Monitoring Board, and serves as an ADCS statistical resource.

Curtis Taylor, Ph.D., Medical Analyst. Reviews, codes and analyzes study medical safety data, disseminates oversight reports, assists in preparing grants, protocols and secondary publications, and serves as an ADCS statistical resource.

Mario Schittini, MD, MPH located in Bronx, NY - Lead Monitor - responsible for management of ADCS Monitoring Group and site monitoring.

Karen Croot, BA located in La Jolla (San Diego), CA - responsible for site monitoring.

Gina Garcia Camilo, MD located in Bronx, NY - responsible for site monitoring.

Kris Gravanda Brugger, MA located in Washington, DC - responsible for site monitoring.

Janet Kastelan, MA located in New York, NY - responsible for site monitoring.

Viviana Messick, BS located in La Jolla (San Diego), CA - responsible for site monitoring.

Alan Pamoleras, BA located in La Jolla (San Diego), CA - responsible for site monitoring.

Rebecca Ryan-Jones, PhD located in St. Petersburg, FL - responsible for site monitoring.

Pamela A. Saunders, PhD located in Washington, DC - responsible for site monitoring.