Senior Medical Writer
About this role
About the Role You will lead the development and execution of medical writing strategies for clinical research projects at ICON, driving clear, accurate scientific communications and supporting the advancement of innovative treatments. This role involves owning medical writing deliverables, collaborating with cross-functional teams, and providing scientific leadership within the medical writing group. What You'll Do
- Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy and clarity.
- Collaborating with cross-functional teams (clinical research, biostatistics, regulatory affairs, medical affairs) to interpret and summarize clinical trial data and scientific findings.
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