Regulatory Affairs CMC Author
Clinical Careers Page(18 days ago)
About this role
ICON plc is hiring a Regulatory Affairs CMC Author to manage global regulatory submission activities for plasma-derived therapies in a highly collaborative, international environment. The role involves maintaining regulatory dossiers, ensuring compliance with global standards, and collaborating with cross-functional teams to support product lifecycle management.
Required Skills
- Regulatory Submissions
- CMC
- ICH Guidelines
- Global Regulatory Requirements
- Documentation Management
- Cross-functional Collaboration
- Regulatory Strategy
- Life Cycle Management
- Dossier Preparation
- Compliance
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.
View more jobs at Clinical Careers Page →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Clinical Careers Page
Similar Jobs
Director, CMC Regulatory Affairs
Capricor Therapeutics(17 days ago)
Regulatory Affairs Consultant
Parexel(25 days ago)
Associate Director, Regulatory Affairs, CMC
BeOne Medicines(9 days ago)
Senior Manager, Regulatory Affairs CMC
MSD(24 days ago)
Senior Director, CMC Regulatory Affairs
Mineralys Therapeutics(18 days ago)
Executive Director, Regulatory CMC
BridgeBio Pharma(7 days ago)