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About the Role:

  • The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support all phases of product development.
  • This role involves organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with ICH guidelines.

What You'll Do:

  • Organize, analyze, interpret, and present scientific and statistical information per ICH and other regulatory guidelines.
  • Collaborate with cross-functional internal and external document production teams.
  • Work under the direction of Medical Writing management.

What We're Looking For:

  • Bachelor's degree in a science-related field with at least 7 years of medical writing experience in a CRO or pharmaceutical setting.
  • Advanced knowledge of ICH and regulatory guidelines, excellent written English, and keen attention to detail.
  • Proficiency in Microsoft Office Suite, including advanced Microsoft Word skills.

What We Offer:

  • Remote working with flexible time off and paid holidays.
  • Medical insurance, tuition reimbursement, and retirement plans.
  • A diverse and inclusive culture with a global team.

Veristat

Veristat is a global contract research organization with over 30 years of expertise accelerating life-changing therapies to patients worldwide. The company has a flexible, inclusive culture with a 70% remote workforce and 66% women-led teams.

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