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

Responsibilities

• Independently oversee all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports
• Provide guidance at the site and project level towards audit readiness standards 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 and recruitment of potential investigators, preparation of EC/IRB submissions, collection and review of regulatory documents, review and adaptation of patient informed consents, notifications to IRB, EC and regulatory authorities, translat...