Regulatory Submissions Manager
Clinical Careers Page(11 days ago)
About this role
This role is for a Regulatory Affairs Manager at ICON, a global clinical research organization, focusing on leading regulatory activities for pharmaceutical projects. The position involves collaborating with internal teams, ensuring compliance with global regulations, and participating in agency interactions to support cutting-edge drug development.
Required Skills
- Regulatory Submissions
- Global Regulatory Requirements
- CTA
- IND
- MAA
- Regulatory Guidance
- Pharmaceutical Industry
- Biotechnology
- Team Leadership
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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