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Brief
Summary of Relevant Clinical Research Experience
A member of the PRI team since 1978, and having
been involved in more than 500 studies, Dr. Wilcox is experienced
in all phases [I-IV] of clinical research. His responsibilities
include the overall conduct (and sometimes design) of clinical
investigations performed at the Institute. Operational
duties include planning, staffing, budgeting, patient recruitment,
fulfillment of and compliance with U.S. and foreign regulatory
requirements, as well as the dissemination (i.e. publication
and presentation) of research results. Clinical responsibilities
include preliminary pre-screening of study participants,
global ratings (i.e. ADAS-Cog., CGIC, CDR and CIBIC-Plus,
etc.), medication accountability and assistance with informed
consent processes.
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