Description
Revolution Medicines is hiring an Associate Director, Regulatory Affairs, Europe to provide regulatory leadership for oncology programs across the EU, EEA, UK, and Switzerland. The role owns end-to-end MAA filing execution, regulatory strategy, dossier readiness, health-authority engagement, risk mitigation, cross-functional alignment, and oversight of external vendors and CROs. It reports to the Director, Regulatory Affairs, Europe and requires a life-sciences or related degree, at least 8 years of pharmaceutical or biotech experience, and at least 7 years in regulatory affairs including regulatory strategy.
