Regulatory Submissions Manager
Clinical Careers Page(13 days ago)
About this role
ICON plc is a global healthcare organization that specializes in clinical research and drug development. They are seeking a Manager, Regulatory Affairs, to lead regulatory activities and provide guidance in the development and approval processes of pharmaceutical and biotech products.
Required Skills
- Regulatory Submissions
- Regulatory Guidance
- CTA
- IND
- MAA
- Global Regulatory Requirements
- Cross-Functional Teamwork
- Clinical Development
- Drug Development
- Regulatory Guidelines
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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