Medical writer

• Provide scientific and medical/clinical writing support as part of a team dedicated to late-phase projects, servicing an assigned client
• Work closely with the ICON team and other members of the client account team to ensure timely delivery of high-quality and scientifically/medically accurate assigned projects
• Work with Peri- and Post-Approval Safety studies and RWE studies
• Write and review study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report
• Develop scientific communications such as abstracts, posters, and manuscripts
• Perform quality control for medical writing deliverables
• Interpret statistical results and solicit statistician input for study reports, abstracts, manuscripts, and other documents
• Participate in improvement of the quality assurance system
• Participate in bid-defence presentations representing medical writing activities

Explore Senior Medical Writer at ICON plc. Review requirements and application details.

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