Senior Clinical Research Associate – Argentina

About the role

We are expanding our clinical research capabilities across Latin America and are looking for a Senior Clinical Research Associate to lead complex studies in Argentina. You will oversee site management, ensure patient safety, and deliver high‑quality data while mentoring junior staff.

Key responsibilities

• Manage all aspects of study site operations, from start‑up to close‑out, ensuring compliance with ICH‑GCP and local regulations.
• Conduct site visits (qualification, initiation, monitoring, close‑out) and prepare accurate monitoring reports.
• Coordinate regulatory submissions, EC/IRB approvals, informed consent processes, and documentation translation.
• Support budget negotiations and investigator contract execution under guidance of the contracts team.
• Monitor patient recruitment, retention, and safety, addressing protocol deviations and pharmacovigilance issues.
• Maintain trial management tools, status reports, and audit‑readiness documentation.

Required profile

• Extensive experience managing complex clinical trials in Argentina or similar markets.
• Proven ability to lead site teams and mentor junior CRAs.
• Strong understanding of local regulatory requirements and ethics committee processes.
• Excellent organizational and communication skills.

Required skills

• ICH‑GCP
• SOP compliance
• Regulatory submissions
• Clinical trial monitoring
• Site management
• Budget negotiation
• Contract management
• Data entry into trial tracking systems

What we offer

• Opportunity to work on high‑impact studies across Latin America.
• Professional growth through mentorship and leadership responsibilities.
• Collaborative environment with experienced clinical operations teams.