About this role
Principal Clinical Trial Regulatory Affairs - +4 years of experience in regulatory submissions in LATAM - Argentina, Mexico or Brazil Home Based at Syneoshealth. Location: Argentina or Brazil or Mexico. Role: managing submissions, leading strategy, mentoring staff Requirements: 4+ years LATAM regulatory submissions experience, knowledge of clinical trial and device regulations and GxPs, budgeting and quality management experience, ability to lead teams and mentor staff; Bachelor’s degree preferred. Category: Research and Development (R&D) Seniority: Mid Level Commitment: Full Time Workplace: Remote Languages: English