Found Description
**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...
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...