Principal Medical Writer
Clinical Careers Page(28 days ago)
About this role
ICON is seeking a Principal Medical Writer to lead the development of high-quality regulatory and clinical documents, supporting clients' submissions to regulatory authorities. The role involves collaboration with cross-functional teams and adherence to industry standards.
Required Skills
- Medical Writing
- Regulatory Submissions
- Clinical Documentation
- Regulatory Affairs
- Scientific Writing
- Clinical Study Reports
- CTD/eCTD
- GxP
- Biostatistics
- Documentation
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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