**Job overview**

This role is responsible for managing importation and customs clearance processes for clinical trial materials, ensuring timely and compliant delivery in line with local regulatory requirements.

The position leads import-related activities during study start-up, supports ongoing compliance during the maintenance phase, and coordinates closely with cross-functional teams to ensure seamless study execution.

**Key Responsibilities**

• Manage importation processes for clinical trial materials, including import permit applications and renewals, throughout the entire study lifecycle (from start-up through study maintenance) in compliance with local regulations

• Manage customs clearance activities specifically for shipments required for site activation (e.g., initial delivery of lab kits, equipment, and clinical trial supplies)

• Prepare and maintain import-related documentation, including import permits and shipping docu...