The Import/Export Specialist supports Site Activation by managing import and export processes for clinical trial materials across LATAM while ensuring compliance with SOPs and maintaining accurate project documentation
Job Summary
The Import/Export Specialist supports Site Activation by managing import and export processes for clinical trial materials across LATAM while ensuring compliance with SOPs and maintaining accurate project documentation.
This role provides local regulatory and logistical expertise to project teams throughout study planning and execution, including direct contact with sponsors on specific initiatives.
IQVIA is a leading global provider of clinical research services and is committed to integrity in the hiring process with a zero tolerance policy for candidate fraud.
Matching Summary
The Import/Export Specialist supports Site Activation by managing import and export processes for clinical trial materials across LATAM while ensuring compliance with SOPs and maintaining accurate project documentation.
Skills & Requirements
Must-have
Import/export processes in LATAM
Compliance with SOPs and WIs
Project documentation and tracking
Brazil import/export experience
Advanced English and Portuguese
Nice-to-have
Knowledge of Argentina and other LATAM countries
Spanish language skills
Good communication and interpersonal skills
Good organizational skills
Quality control of documents
Key Requirements
At least 1 year international trade experience in clinical trials