Clinical Research Associate role in Buenos Aires supporting clinical trial conduct across assigned sites. The position manages site relationships, ensures regulatory compliance with ICH-GCP standards, performs monitoring activities, and develops new research sites while reporting to a CRA manager.
Responsibilities
Build and maintain strong site relationships throughout all trial phases
Perform remote and on-site monitoring to ensure data quality, accuracy and subject safety
Conduct site visits including initiation, monitoring and close-out visits with comprehensive documentation
Manage regulatory documentation for study start-up, maintenance and close-out
Identify and resolve site performance or compliance issues through escalation pathways




Requirements
2+ years direct site management or monitoring experience in biotech, pharma, or CRO
Fluent in English, verbal and written communication
Bachelor's degree with strong emphasis in science or biology
Working knowledge of GCP/ICH guidelines and country clinical research regulations
Demonstrated site management and patient recruitment skills
Proficiency with MS Office and clinical IT applications
Strong organizational, time management, and problem-solving abilities

📌 Clinical Research Associate (Buenos Aires)
🏢 Merck
📍 Buenos Aires