Non clinical Regulatory Document and Scientific Writer

US Tech Solutions

Contract Media and Communication Workers
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Location
Madison, New Jersey, United States
Posted
July 04, 2026

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...

    • Job Details

    • Job Type
      Contract
    • Category
      Media and Communication Workers
    • Date Posted
      July 04, 2026
    • Application Deadline
      August 13, 2026