Regulatory Affairs Specialist
Clinical Careers Page(1 month ago)
About this role
A Regulatory Affairs Specialist at ICON supports the company’s clinical research activities by ensuring regulatory compliance for clinical trials in Brazil and the region. The role is part of ICON’s broader healthcare intelligence and clinical development organization, working in a hybrid capacity from São Paulo to support high-quality, ethical clinical research.
Required Skills
- Clinical Submissions
- Regulatory Affairs
- ANVISA
- CTMS
- eTMF
- Translation Management
- Project Coordination
- Stakeholder Interaction
- Budget Management
- Training
+1 more
About Clinical Careers Page
iconplc.comICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
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