-
Ability
to provide, quality work at clinical research site
-
Ability to conduct Phase II through Phase IV
studies
-
Highly skilled, experienced
and enthusiastic Investigators
-
Dedicated, full time, and experienced
Clinical Research Coordinators
-
Access to large patient populations with
cultural diversity
-
Efficient and centralized contract and budget
resolution
-
Ability to conduct inpatient and outpatient
studies
-
Strong working relationships with local and
central IRBs and laboratories
-
Stable, effective and mutually beneficial
working relationships with referring physicians
