Senior Regulatory Affairs Specialist
ICON · Sao Paulo, Brazil
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Role summary
ICON seeks a Senior Regulatory Affairs Specialist for its São Paulo office to manage clinical trial regulatory submissions and interactions with Brazilian authorities, including ANVISA. The role involves preparing and coordinating submission documentation, tracking approvals, and collaborating across teams on regulatory deliverables. Candidates need 4+ years of clinical trial submission experience, fluent English, and knowledge of local regulatory requirements.
Privacy & handoff
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