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Medical Writer - Remote

Posted 15 weeks ago

C.B

Cogent Biosciences

Writing
Full Time
USA

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Overview

We are seeking an experienced, collaborative, detail-oriented medical writer with a passion for medical writing. The successful candidate will lead the planning, authoring, reviewing, and QC of clinical and regulatory documents.

In Short

  • Lead the planning and authoring of clinical and regulatory documents.
  • Review and ensure quality control of documents.
  • Collaborate with cross-functional subject matter experts.
  • Work independently to develop high-quality, scientifically accurate documents.
  • Oversee the work of contract writers.
  • Contribute to medical writing process development.
  • Passion for medical writing.
  • Detail-oriented and collaborative approach.
  • Experience in the biotechnology or pharmaceutical industry.
  • Strong communication skills.

Requirements

  • Proven experience in medical writing.
  • Strong understanding of clinical and regulatory documentation.
  • Ability to work with cross-functional teams.
  • Excellent writing and editing skills.
  • Detail-oriented with a focus on quality.
  • Experience overseeing contract writers is a plus.
  • Knowledge of the biotechnology industry.
  • Ability to manage multiple projects simultaneously.
  • Strong organizational skills.
  • Ability to work independently and as part of a team.

Benefits

  • Opportunity to work in a leading biotechnology company.
  • Collaborative work environment.
  • Contribute to meaningful medical advancements.
  • Professional development opportunities.
  • Competitive salary and benefits package.
  • Work with a passionate team.
  • Flexible work arrangements.
  • Access to cutting-edge research.
  • Supportive company culture.
  • Engagement in innovative projects.

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