Lead Medical Writer

Clinical Careers Page(25 days ago)

RemoteFull TimeSenior$133,313 - $180,428 (estimated)Medical Writing

About this role

A Senior Medical Writer at ICON leads the creation and oversight of clinical and regulatory documents to support clinical development programs. The role contributes to scientific communication and dissemination of study results within a global CRO environment. This position emphasizes scientific accuracy, regulatory compliance, and clear presentation of clinical data.

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Required Skills

Medical Writing
Regulatory Writing
Clinical Protocols
Clinical Study Reports
Regulatory Submissions
Data Interpretation
Publication Planning
Scientific Communication
Mentoring

Qualifications

Master's Degree
PhD
PharmD
MD

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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