Regulatory Affairs Manager
Clinical Careers Page(1 month ago)
About this role
A Manager, Regulatory Affairs at ICON is a member of the Regulatory Affairs team supporting drug development and regulatory strategy for clinical programs. This home-based role in South Korea contributes to regulatory planning across development stages and engagement with global regulatory authorities. The position is within ICON, a global clinical research organization focused on healthcare intelligence and clinical development.
Required Skills
- Regulatory Submissions
- CTA/IND/MAA
- Regulatory Guidance
- Agency Interactions
- Team Leadership
- Global Regulations
- Clinical Development
- Cross-Functional Collaboration
Qualifications
- Bachelor's Degree
- Advanced Degree Preferred
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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