**Responsible for overseeing clinical trial budgets and leading negotiation activities on a global scale**

**Essential Functions**

+ Preparation, review, negotiation and management of site regulatory documentation and clinical trial agreements with sites and sponsors
+ Maintains, reviews, and reports on site activation performance metrics
+ Serves as the primary point of contact for investigative sites and/or sponsors;
+ Ensures tracking completion of all regulatory and contractual documents for sites
+ Establishes project timelines.
+ Ensures all site activation activities are performed in accordance with all regulations, SOPs, Work Instructions and project requirements either at the global, regional, or country level and all relevant documents are submitted timely to the Trial Master File as per IQVIA/Sponsor requirements.
+ Establishes and/or executes goals and objectives for team(s) as well as tracking and delivering on operational/financial perf...