IQVIA

Site Activation Analyst

📍 Location

Bogotá, Bogota

⏰ Job Type

Full time

📅 Posted

June 04, 2026

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Job Description

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 doc...
    

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