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Non clinical Regulatory Document and Scientific Writer

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US Tech Solutions
📍 Madison, United States
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Location Madison
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Posted June 07, 2026
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Commute Local Area
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Job Description


Duration: Months Contract
 

Summary
  • Reporting to the Program Management Lead, the incumbent will be part of the late development translational group based in NJ and will be responsible for writing scientific documents including biomarker reports, regulatory documents (eg, non-clinical summaries, translational portions of clinical/pharmacology summaries, briefing books, CSRs, investigator brochures) in conjunction with Translational scientists. This individual will also contribute to abstracts, posters, manuscript and other scientific communications arising from the group.
    • Technical Skills
  • In-depth understanding of hematological malignancies or solid tumors or Neuroscience disorders especially the clinical landscape, evolving therapy, competitive scenarios
  • Strong understanding of clinical, translational and mechanistic data with Client assets and Client agents
  • Strong background in writing and in communication strategy...

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    📍 Location Details

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    City
    Madison
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    Country
    United States
    🚗
    Commute
    Local Area

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