**Job Description**

**CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS:**

**Illinois, Colorado, South Florida, New York, California, Houston, Dallas**

+ The role is accountable for performance and compliance for assigned protocols and sites in a country.
+ Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally.
+ Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
+ Actively develops and expands the territory for clinical research, finding and developing new sites.
+ Participates in internal meetings and workstreams as SME for monitoring processes and
+ Systems.
**Responsibilities include, but are not limited to:**

+ Develops strong site relationsh...