**Job Overview**

Under general supervision, performs activities at a country/region level associated with **import and export processes for clinical trials** , in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), and project requirements. Responsibilities include feasibility assessments, regulatory submissions, and maintenance activities related to investigational product (IP) logistics.

**Essential Functions**

+ Under general supervision, execute **import/export feasibility, regulatory submissions, and maintenance activities** for assigned studies, ensuring compliance with applicable regulations, SOPs, and work instructions.
+ Prepare and review **import/export documentation** , ensuring completeness, accuracy, and compliance with regulatory and customs requirements.
+ Track, coordinate, and follow up on **approvals and execution of import/export-related documents** , including licenses, permi...