Regulatory Affairs Specialist
Clinical Careers Page(19 days ago)
About this role
ICON plc is seeking a Regulatory Affairs Specialist to support clinical trial programs within the pharmaceutical, biotech, or biologics sectors. The role involves contributing to regulatory submissions and collaborating across teams to ensure compliance and successful regulatory processes, ultimately supporting the development of innovative treatments.
Required Skills
- Regulatory Submissions
- Clinical Trials
- Pharmaceutical
- Biotech
- Regulatory Affairs
- Documentation
- Label Review
- Translation
- Compliance
- Medical Data
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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