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ExecutiveFull-time
VP, Regulatory Affairs
Own global regulatory strategy across a rare disease pipeline approaching late-stage submissions.
Company
Avela Medicines
Location
London, UK · Hybrid
Salary
£160–195k + equity
Posted
1 week ago
Responsibilities
- Define and execute global regulatory strategy
- Lead FDA, EMA and MHRA interactions
- Own submission readiness across CTA, IND, MAA and BLA
Requirements
- 15+ years regulatory affairs across US and EU
- Major submission leadership experience
- Rare disease or orphan drug expertise preferred