Clinical Regulatory Writer (FT, mostly from home)

Job Title:
Clinical Regulatory Writer

Full time, Work from home but must be commutable to northern New Jersey for monthly meetings

Job Description:

  • Must be available to come into the office for meetings monthly
  • Minimum hours per week – 30 hours – Full 40 hours preferred
  • Therapeutic focus: Immunology, Oncology, and Hematology
  • Phases II-IV

Documents will include:

  • Clinical Study Reports
  • CTD Summary Documents
  • Investigator Brochures
  • Briefing books

***Submission documents are preferred. Experience in the past supporting NDA/BLA filings

Contact: Laura Walton –

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