Clinical Research Associate (Site Director) - Argentina

About the role

Codera, a Tang Capital company providing end-to-end drug development services, is hiring a Site Director, Clinical Operations for Argentina. The role manages overall clinical site activity, from site identification and start-up through monitoring, close-out and inspection readiness, ensuring patient safety, rights and well-being and complete, accurate data. Candidates based in Argentina are preferred, and must be able to travel frequently (50-65%); relocation is not required.

Key responsibilities

• Manage and monitor Phase I-IV studies at assigned sites, acting as the main point of contact from start-up to close-out
• Carry out site monitoring, source data verification and remote data review and query resolution
• Complete feasibility and site identification, and prepare documents for regulatory and IRB/EC submissions
• Negotiate site budgets and contracts, and develop recruitment, retention and follow-up plans
• Support site audits and inspections, and escalate site performance or quality issues
• Share best practices, coach colleagues and help improve Codera's systems and procedures

Required profile

• Bachelor's degree in a life science discipline; nursing or RN is a plus
• At least 3 years of direct site monitoring experience
• Bilingual in English and French
• Understanding of ICH-GCP, FDA and local regulations, and of drug development
• Willingness to travel 50-65%, with proximity to a major airport and flexibility for multi-day trips

Required skills

• Proficiency in CTMS and eTMF systems preferred
• Interpretation of study-level metrics and risk mitigation across the study lifecycle
• Excellent written and verbal communication and teamwork skills

What we offer

• Estimated annual base salary of $160,000-$210,000, with possible discretionary bonuses
• Medical, dental and vision insurance, generous paid time off, retirement options and wellness and professional development programs