**Description of Roles and Responsibilities**

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Sponsor policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the SCOM or CRD, the person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure Site Ready.

**Responsibilities include but are not limited to:**

+ Ownership of country and site budgets. Development, negotiation, and completion of Clinical Trial Research Agreements (CTRA).
+ Oversees and tracks clinical research-related payments. Payment reconciliation at study close-out. Oversees FCPA, DPS/OFAC, and maintenance of financial systems. Experience Required • 5-7 years of experience in clinical research or combined experience in Clinical Research and F...