We’re expanding our capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re hiring a Safety Specialist to join our growing team!

Main Duties & Responsibilities Process IC&S according to SOPs and project‑specific safety plans Triages IC&S, evaluates data for completeness and regulatory reportability Enter data into Argus Safety Database Code events, medical history, concomitant meds, and tests Draft case narratives Query resolution and follow‑up until complete Generate timely expedited regulatory reports Coordinate reconciliation of safety and clinical databases Ensure required safety reports distribution Participate in audits/inspections Submit documents to TMF/PV System MF Maintain compliance with SOPs, GCP, ICH, GVP, regulations Attend department meetings Participate in project meetings Other duties as assigned Education And Experience

Minimum Education & Experience:

Minimum 2 years clinical trial drug safety experience; Bachelor’s degree...