Associate Director Regulatory Affairs

Clinical-Stage Precision Medicine Biotech | Bay Area

We’re partnering with a high-growth, clinical-stage biotech using human genetics to develop precision small-molecule medicines across renal, cardiovascular and metabolic diseases.

This is a hands-on Associate Director role with real ownership — supporting global regulatory strategy and execution across multiple clinical programs, working closely with Clinical, CMC and Biometrics teams, and engaging directly with Health Authorities.

Key highlights:

• Regulatory lead for assigned clinical-stage programs
• Hands-on ownership of INDs / CTAs, amendments and HA interactions
• Strong cross-functional exposure and visibility to senior leadership
• Science-driven culture with a growing, well-funded pipeline
• ~7+ years’ Regulatory Affairs experience in biotech/pharma
• Strong US/EU regulatory knowledge and ICH experience
• Up to $240,000 base salary dependent on experience
• Annual performance bonus + equity
• 401(k) with employer match
• Generous PTO and holiday policy

A rare opportunity to step into a high-impact regulatory role within a genuinely innovative precision medicine company.

Should this opportunity spark some interest, please apply with a copy of your CV to set up a confidential discussion.