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 site start‑up, including feasibility, IRB/EC submissions, regulatory document review, and investigator contract negotiation.
• Conduct pre‑study, initiation, routine monitoring, and close‑out visits in line with protocol, local laws, ICH‑GCP and company SOPs.
• Maintain trial management tools, status reports, and ensure audit readiness at site and project levels.
• Verify informed consent processes, assess protocol deviations, and address pharmacovigilance issues.
• Prepare accurate monitoring reports, documentation, and support recruitment and retention strategies.

Required profile

• Extensive experience managing complex clinical trials in a senior CRA capacity.
• Proven ability to work independently and support Clinical Trial Managers or Project Managers.
• Strong communication skills for training and mentoring junior staff.

Required skills

• ICH‑GCP compliance
• Clinical monitoring and site management
• Regulatory submissions and documentation
• Use of trial management tools/systems
• Budget negotiation and contract execution

What we offer

• Opportunity to lead high‑impact studies across Latin America.
• Collaborative environment with professional growth and mentorship.