Startups · AI

Associate Director, Regulatory & Medical Writing

Nurix AI · Brisbane, California · On-site

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About Nurix AI

AI agents that run your enterprise workflows and get measurably better over time. 150+ enterprises live in production across retail, insurance, and financial services. Backed by Accel and General Catalyst.

About the role

Help shape how Nurix communicates its science to health authorities and the world. As Associate Director, Regulatory & Medical Writing, you’ll independently lead the authoring, review, and approval of critical regulatory documents across our pipeline — from clinical protocols to health authority submissions. It’s a chance to bring clarity and strategic messaging to the documents that move our therapies through development and toward patients.

What they're looking for

  • Clinical study protocols and clinical protocol amendments
  • Clinical study reports
  • Investigator’s brochures and annual updates
  • IND submissions and annual reports
  • Lay-person summaries
  • Integrated summary reports
More about this role

Help shape how Nurix communicates its science to health authorities and the world. As Associate Director, Regulatory & Medical Writing, you’ll independently lead the authoring, review, and approval of critical regulatory documents across our pipeline — from clinical protocols to health authority submissions. It’s a chance to bring clarity and strategic messaging to the documents that move our therapies through development and toward patients.

  • Author and manage authoring of Regulatory & Medical Writing documents together with cross-functional collaborators; ensure content consistency within a document and across documents for a particular asset, including the development of strategic messaging and data presentation in accordance with Nurix standards and health authority requirements, for documents such as:
  • Clinical study protocols and clinical protocol amendments
  • Clinical study reports
  • Investigator’s brochures and annual updates
  • IND submissions and annual reports
  • Lay-person summaries
  • Integrated summary reports
  • Clinical, nonclinical, and multidisciplinary information amendments
  • NDA, BLA, MAA, and (e)CTD submissions
  • Risk Management Plans
  • Health authority...

Read the full posting on Nurix AI's site ↗

Regulatory

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