Principal Medical Writer

Clinical Careers Page(1 month ago)

HybridFull TimeSenior$169,117 - $226,417 (estimated)Medical Writing

About this role

A Principal Medical Writer at ICON leads the creation of high-quality regulatory and clinical documents to support client submissions to global regulatory authorities. The role focuses on authoring Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and Clinical Overviews in line with ICH and other global guidelines. The position collaborates with cross-functional teams to manage timelines and ensure compliance with industry standards and study objectives.

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Required Skills

Medical Writing
Regulatory Writing
Clinical Writing
Clinical Study Reports
Protocol Review
Project Management
Communications
Time Management
Cross-Functional Collaboration
Regulatory Knowledge

+1 more

Qualifications

Bachelor's Degree in Life Science
Master's Degree in Life Science (Preferred)

About Clinical Careers Page

iconplc.com

ICON 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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