senior medical writer
Clinical Careers Page(2 months ago)
About this role
A Senior Medical Writer at ICON leads the development and medical writing strategy for clinical research projects, contributing to the preparation of regulatory and clinical documents that support drug development. The role is based in Tokyo/Osaka with hybrid work options and supports the communication of scientific findings through publications and regulatory submissions. The position works closely with cross-functional teams to advance clinical development and mentor junior writers.
Required Skills
- Medical Writing
- Regulatory Submissions
- Clinical Protocols
- Clinical Study Reports
- Investigator Brochures
- Data Interpretation
- Scientific Writing
- Publication Planning
- Mentoring
- Project Management
Qualifications
- Bachelor's Degree
- Advanced Degree in Life Sciences, Pharmacy, or Medicine
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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