ICON seeks a Clinical Study Assistant to support pharmaceutical clinical trial planning and execution in Mexico City on a remote basis. The role involves regulatory compliance, documentation review, monitoring oversight, and cross-functional collaboration with study teams and external organizations.
Responsibilities
Support critical day-to-day clinical study activities and regulatory inspection readiness
Review study documentation including essential packets, protocols, and informed consent forms
Collaborate with Clinical Operations teams, study managers, and CROs on study execution
Support risk-based monitoring oversight and clinical trial system activities
Assist with vendor contract administration and study close-out financial reconciliation
Requirements
Bachelor's degree in scientific or healthcare-related field
1-2 years pharmaceutical industry or clinical research organization experience
Knowledge of integral and regional regulatory compliance for clinical research
Fluent business English, oral and written
Strong task management and cross-functional collaboration skills
Excellent organizational, interpersonal, and problem-solving abilities
Willingness to travel approximately 10% as required

📌 Clinical Study Assistant (Xico)
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📍 Xico