Clinical Research Associate – Site Management

About the role

Join a global healthcare leader as a Clinical Research Associate, responsible for performance and compliance of assigned protocols and sites in Argentina. You will act as the primary site contact, ensuring study conduct aligns with ICH/GCP, local regulations, and company standards.

Key responsibilities

• Develop and maintain strong site relationships throughout all trial phases.
• Perform site monitoring activities (remote and on‑site) in compliance with ICH‑GCP, SOPs, and local laws.
• Coordinate site start‑up, regulatory documentation, and ongoing study maintenance.
• Conduct site visits (validation, initiation, monitoring, close‑out) and produce accurate visit reports.
• Identify and resolve site performance or compliance issues, escalating as needed.
• Maintain study data in CTMS, eTMF and other systems.
• Contribute to site selection, validation, and expansion of the clinical research territory.

Required profile

• Minimum 2 years of direct site management (monitoring) experience in bio/pharma or CRO.
• Fluent in English (verbal and written) with strong communication skills.
• Bachelor’s degree with a strong emphasis in science or biology.
• Ability to work independently across multiple protocols and therapy areas.

Required skills

• Knowledge of ICH/GCP guidelines and local clinical research regulations.
• Experience with CTMS and electronic Trial Master File (eTMF) systems.
• Proficiency in Microsoft Office and various clinical IT applications on computers, tablets, and mobile devices.
• Good documentation practices and data/metric analysis capabilities.