We're expanding our capabilities across Latin America, and we're hiring a Senior Clinical Research Associate to support critical studies across Argentina!

As a Senior CRA you'll possess a wide-ranging and broad experience handling our most complex and advanced assignments.

Responsibilities

• Oversee all aspects of study site management to ensure patient safety and quality of data with consistently low query levels.
• Provide guidance at the site and project level toward audit readiness and support preparation for audit and required follow-up actions.
• Establish, update, track and maintain study‑specific trial management tools/systems and status reports.
• Manage site start‑up procedures including feasibility, recruitment of prospective investigators, EC/IRB submissions, regulatory document review, adaptation of patient informed consents, notifications, translation, meetings, and other tasks directed by Clinical Trial or Project Mana...