Study Coordinator - Beunos Aires, Argentina

ProPharma seeks a Study Coordinator based in Buenos Aires to support remote clinical research site activities. The role involves managing day-to-day site communications, subject recruitment, protocol execution, data management, and regulatory compliance across assigned projects.

Responsibilities

• Serve as primary contact for site communications, document submissions, and activity coordination
• Support subject recruitment, screening, re-consenting, and medical record acquisition
• Execute protocol-directed activities and maintain compliance with IRB and FDA documentation standards
• Perform data entry, address database queries, and monitor clinical information systems
• Assist with study closeout and other assigned site-related activities

Requirements

• Bachelor's degree or 2+ years of related clinical research or study team experience
• Knowledge of ICH-GCP guidelines and applicable regulatory requirements
• Proficiency with PC-based technology and web-based research platforms
• Strong written and verbal communication skills
• Ability to maintain independent workspace with privacy and security
• Excellent organizational skills with capacity to multitask and manage competing priorities