About this role
Regulatory Affairs Specialist (Australia) at Alimentiv-2. Location: Sydney or Australia. Role: managing submissions, conducting reviews, advising stakeholders Requirements: Undergraduate degree and 4+ years clinical research/regulatory affairs experience; knowledge of LATAM clinical trial regulations; fluency in English and Spanish; experience managing clinical trial submissions and regulatory risk assessments. Category: Research and Development (R&D) Seniority: Mid Level Commitment: Full Time Workplace: Remote Languages: English, Spanish