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🥝 Associate Director, CMC Regulatory Affairs

Recursion | London, United Kingdom | Posted June 14, 2026

Associate Director, CMC Regulatory Affairs

Job Description

Your work will change lives. Including your own.

The Impact You’ll Make
  • Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications.
  • Influence the regulatory strategy of Recursion’s development programs by attending team meetings, providing drug substance or drug product recommendations for US, EU and Rest of World (ROW) regulatory requirements/guidance interpretation, and best practices for CMC submissions and meetings.
  • Strategize, plan, write, manage internal and external contributors and review region specific investigational stage CMC summary submission documents (Module 2, Module 3, IMPD, etc.) and agency requests.
  • Deliver high quality regulatory US, EU and ROW submissions, strategy and advice.
  • Support review of investigational product labels, protocols, investigator’s brochure, and other clinical trial materials; GM...

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