Freelance Regulatory & Study Start-Up Specialist – LATAM - Brazil, Chile and Argentina Upsilon Global are seeking a freelance regulatory and start-up specialist with solid experience in Ethics Committee submissions for observational studies in LATAM, specifically Chile, Argentina and Brazil. The role will provide centralized oversight and execution of local submissions across the three countries to ensure quality, consistency and timeline adherence. Key Details: Start Date: February 2026 Contract Length: 6 months initially FTE: Approximately 0.5 FTE Therapeutic Area: Observational/RWE - infectious diseases Location: Remote, covering Brazil, Argentina and Chile Key Responsibilities: Manage regulatory submissions and site start-up activities. Ensure compliance with Swiss and international clinical trial regulations. Liaise with sponsors, investigators, and ethics committees. Track approval timelines and maintain regulatory documentation. Provide guidance on regulatory requirements and study compliance. Requirements: EC submissions for observational studies Experience managing submissions across multiple countries Familiarity with projects including satellite sites Proactive and solution-oriented Strong sense of ownership and accountability Ability to work under tight timelines Fluency in English with Spanish/Portuguese beneficial Experience: EC submission expertise Knowledge of LATAM regulatory landscapes Hands-on experience with EC submissions in LATAM Ability to work independently and drive submissions end-to-end Strong coordination and stakeholder management skills Please apply via the link, or contact +44 203 875 9966 / applications@upsilonglobal.com