Study Coordinator - Beunos Aires, Argentina
ProPharma Group · US
Clinical OperationsPart-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Privacy & handoff
This role links to ProPharma Group's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.