About this role
Regulatory Affairs Officer, IQVIA Biotech at Iqvia. Location: Buenos Aires or Mexico City or São Paulo. Role: leading teams, drafting documents, engaging authorities Requirements: Bachelor's or Master's in life sciences; 3–4 years clinical trial regulatory experience in CRO/biotech/pharma; experience with EU CTR, Health Canada, US FDA IND pathways; proficiency with Microsoft Office and eCTD systems; strong communication and project management skills. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Office, eCTD systems Commitment: Full Time Workplace: Onsite Languages: English