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Lead Medical Writer

icon · Sao Paulo

New
Senior 🇬🇧 English
Medical writing Clinical study reports Regulatory submissions ICH-GCP FDA EMA

Job description

About the role

ICON Strategic Solutions is hiring a Lead Medical Writer in Sao Paulo, working in a sponsor-dedicated model supported by ICON's global expertise. As a Senior Medical Writer, you will lead the development and execution of medical writing strategies for clinical research projects, helping advance treatments that benefit patients worldwide.

Key responsibilities

  • Take ownership of medical writing deliverables and apply your expertise to complex challenges.
  • Lead the preparation, review and editing of clinical study documents such as protocols, clinical study reports (CSRs), investigator brochures (IBs) and regulatory submissions, ensuring accuracy and clarity.
  • Work with clinical research, biostatistics, regulatory affairs and medical affairs teams to interpret and analyse clinical trial data and summarise scientific findings.
  • Contribute to the planning and execution of clinical development programmes, giving strategic input on the design, conduct and interpretation of clinical studies.
  • Help develop publication plans, abstracts, posters and manuscripts for peer-reviewed journals and scientific conferences.
  • Mentor and coach junior medical writers on best practices, writing techniques and scientific principles.

Required profile

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
  • Strong foundation in medical writing, with the experience to work independently and guide others.
  • Ability to work in a fast-paced, deadline-driven environment and manage multiple projects at once.
  • Excellent interpersonal and communication skills and the ability to influence decision-making with cross-functional teams.
  • Legal right to work in the country where the role is based.

Required skills

  • Interpreting and summarising complex clinical trial data, research findings and statistical analyses.
  • Writing, editing and proofreading.
  • Understanding of regulatory requirements such as ICH-GCP, FDA and EMA, and experience interacting with regulatory agencies.

What we offer

  • Competitive base salary and performance-related incentives.
  • Health and wellbeing programmes, including medical, dental and vision coverage where applicable.
  • Retirement and pension plans, life assurance and disability coverage.
  • Employee assistance programmes and learning and development opportunities.

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Source : ats:workday

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Published 11 hours ago

Expires 1 month from now

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Sao Paulo