Senior Scientific Writer — Regulatory & Translational Docs

A leading consulting group is seeking a Nonclinical Regulatory Document and Scientific Writer in Madison, NJ. This role involves developing high-quality scientific and regulatory documents in collaboration with Translational scientists, supporting late-stage drug development. The ideal candidate should have a Master’s or PhD in Hematology, Oncology, or Neuroscience, along with 6–8 years of relevant experience. Strong communication, project management, and collaboration skills are essential. The position features a hybrid work schedule.
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