Senior Regulatory Affairs Specialist
Clinical Careers Page(2 months ago)
About this role
A Senior Regulatory Affairs Specialist at ICON plc based in South Korea supports the regulatory function for clinical development and product registration. The role focuses on aligning local regulatory activities with corporate and global strategies, monitoring regulatory developments, and collaborating with cross-functional teams to enable compliant clinical operations and registrations.
Required Skills
- Regulatory Submissions
- Regulatory Strategy
- Regulatory Compliance
- Regulatory Intelligence
- Stakeholder Relations
- Clinical Trials
- Licensing
- Change Control
- Project Management
- Documentation
+2 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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