Regulatory Affairs Manager
Clinical Careers Page(20 days ago)
About this role
ICON plc is a leading clinical research organization specializing in healthcare intelligence. They are seeking a Regulatory Affairs Manager (CMC Author) to oversee global CMC regulatory strategies and submissions for pharmaceutical products, supporting development, market launch, and lifecycle management.
Required Skills
- Regulatory Submissions
- CMC
- ICH Standards
- Global Regulatory Environment
- Drug Development
- Regulatory Strategy
- Authoring
- Document Management
- Cross-functional Collaboration
- Pharmaceutical Industry
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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