Regulatory Submissions Manager-Kazakhstan
Clinical Careers Page(5 days ago)
About this role
ICON plc is a leading healthcare intelligence and clinical research organization committed to innovation and excellence in clinical development. They are seeking a Regulatory Submissions Manager to lead regulatory activities and support drug development processes. The role involves guiding teams, participating in agency interactions, and ensuring compliance with regulatory guidelines.
Required Skills
- Regulatory Submissions
- Regulatory Affairs
- Clinical Trials
- Agency Interactions
- Global Guidelines
- Drug Development
- Regulatory Strategy
- Biotechnology
- Pharmaceuticals
- 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.
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