Sr. Regulatory Affairs, Study Start Up Specialist

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr. Regulatory Affairs, Study Start Up Specialist based in Brazil. This role offers the opportunity to support the successful launch and execution of global clinical trials by managing complex regulatory activities across multiple countries. You will play a key part in ensuring clinical studies meet regulatory requirements, quality standards, and submission timelines. Working within a collaborative international environment, you will partner with project teams, sponsors, sites, and regulatory bodies to advance innovative treatments for patients with critical and chronic conditions. The position combines regulatory expertise, operational coordination, and quality oversight. You will contribute to improving processes, mentoring colleagues, and ensuring excellence throughout the clinical trial lifecycle.