Associate Director, Regulatory Operations And Intelligence

Recursionpharmaceuticals

United States
Base: $176,400 - $240,800; bonus/equity: annual bo...
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Global regulatory submissions
Regulatory documentation management
Regulatory intelligence gathering
** Recursion Pharmaceuticals is seeking an Associate Director for Regulatory Operations and Intelligence to manage global regulatory submissions, oversee documentation processes, and gather regulatory intelligence. The ideal candidate will have extensive experience in regulatory publishing and a strong understanding of FDA submissions, with a focus on collaboration and strategic decision-making. **

Job Summary

  • This role will play a critical role in supporting global regulatory submissions, overseeing submission processes, managing regulatory documentation and gathering regulatory intel to keep programs and organization updated with latest regulatory trends.
  • You will collaborate with Regulatory Leads to support the development of submission/content plans, format and publish regulatory documents, and independently lead, monitor, analyze, and interpret global regulatory developments.
  • The estimated current annual base range for this role is $176,400 - $240,800 (USD), and you will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package.

Matching Summary

Match Score: 75

** Recursion Pharmaceuticals is seeking an Associate Director for Regulatory Operations and Intelligence to manage global regulatory submissions, oversee documentation processes, and gather regulatory intelligence. The ideal candidate will have extensive experience in regulatory publishing and a strong understanding of FDA submissions, with a focus on collaboration and strategic decision-making. **

Salary

Base: $176,400 - $240,800; Bonus/Equity: Annual bonus and equity compensation; Benefits: Comprehensive benefits package

Skills & Requirements

Must-have

  • global regulatory submissions
  • regulatory documentation management
  • regulatory intelligence gathering
  • submission publishing systems
  • CTD/eCTD dossier creation
  • health authority interaction

Nice-to-have

  • critical thinking
  • attention to detail
  • cross-functional collaboration
  • technical writing
  • project management

Key Requirements

  • Master's or Bachelor's degree in a scientific discipline
  • 7+ years of industry-related experience
  • 5+ years of experience with specialized regulatory submission and publishing systems
  • Experience with setting up regulatory intelligence functions and tools
  • Experience in FDA regulatory submissions for drugs

Work Rights

Not specified

Tailored Resume

Cover Letter