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Role Overview:
- Lead CMC regulatory strategy for small molecule investigational drugs.
- Influence regulatory strategy by providing guidance for US, EU, and ROW requirements.
Key Responsibilities:
- Strategize, write, and manage CMC submission documents (Module 2, Module 3, IMPD).
- Deliver high-quality regulatory submissions and support GMP inspections.
Qualifications:
- Deep technical knowledge of small molecule drug development.
- 8+ years of CMC regulatory experience with US and EU submission track record.
Compensation:
- Estimated annual base salary range: £111,100–£141,800.
- Eligible for annual bonus, equity, and comprehensive benefits.
Recursion
Recursion is a clinical-stage TechBio company decoding biology to radically improve lives. The company employs a global team and fosters a culture of bold action, care, and collaboration.