Upsilon Global
Upsilon Global está com vaga(s) de emprego para Regulatory Affairs Specialist para Amazonas em Amazonas
Cargo:
Regulatory Affairs Specialist – Amazonas – Upsilon Global
Requisitos:
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 /
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