This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Regulatory Affairs Specialist based in Brazil. This role offers the opportunity to support global clinical research programs by ensuring regulatory compliance, operational excellence, and high-quality service delivery.You will manage regulatory submissions, interpret evolving requirements, and provide expert guidance to internal teams, clients, and external stakeholders.The position combines regulatory expertise, project coordination, and strategic thinking within an international clinical research environment.You will contribute to the successful execution of clinical trials by ensuring documentation, processes, and submissions meet industry standards.This role is ideal for a regulatory professional who enjoys collaboration, continuous learning, and solving complex compliance challenges.You will have the opportunity to influence regulatory strategies while supporting impactful healthcare and research initiatives.