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. The role combines study start‑up, on‑site monitoring and ongoing site management to ensure patient safety and high‑quality data.

Key responsibilities

• Oversee all aspects of site management, from feasibility and investigator recruitment to EC/IRB submissions and regulatory documentation.
• Conduct pre‑study, initiation, routine monitoring and close‑out visits in accordance with protocol, local laws, ICH‑GCP and company SOPs.
• Prepare accurate monitoring reports, confirmation letters and other required documentation.
• Support audit readiness, assist with budget negotiations and investigator contract execution.
• Verify informed consent processes and assess safety or data‑integrity issues at each site.
• Mentor junior CRA staff and provide guidance to Clinical Trial Managers or Project Managers.
• Enter and track data in trial management systems to support recruitment, retention and reporting.

Required profile

• Extensive experience managing complex clinical trials in a CRO or pharmaceutical environment.
• Proven ability to work independently and support senior project leadership.
• Experience training and mentoring junior staff members.
• Strong understanding of local regulatory requirements in Argentina.

Required skills

• ICH‑GCP knowledge
• Clinical trial monitoring
• Site management
• Regulatory compliance
• Budget negotiation