Senior Director, Head of Regulatory & Medical Writing

nurix · Brisbane, California, United States

Posted
12 days ago
Last confirmed live
Today

What this role involves

Nurix Therapeutics is seeking a Sr. Director, Head of Regulatory & Medical Writing to lead regulatory writing strategy and manage a team of internal and external writers. The role involves authoring and editing key regulatory documents for clinical trials and submissions, and reporting to the SVP, Head of Regulatory Affairs. The position requires expertise in regulatory writing and collaboration with cross-functional teams.

Skills this posting asks for

  • regulatory writing
  • medical writing
  • clinical study protocols
  • clinical study reports
  • investigator's brochures
  • ind submissions
  • nda
  • bla
  • maa
  • ectd submissions
  • risk management plans
  • health authority responses
  • briefing documents
  • biometrics
  • tfls

Requirements

  • Level: director

From the employer’s posting

  Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and…

Read the full description on nurix’s careers page

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