Senior Director, Regulatory Affairs, Pulmovant
Pulmovant
- Experience
- 15+ yrs
- Location
- United States
- Job type
- Full-time
Required skills
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Adobe
- Microsoft SharePoint
- Veeva
About the role
BS in scientific field with 15+ years regulatory affairs, or MS with 12-15 years, or PhD/PharmD with 8 years; recent NDA submission experience; FDA experience essential; RAC certification a plus; proficiency in Microsoft Office and SharePoint.
About Pulmovant
Roivant-backed clinical-stage biotechnology company developing inhaled therapies for patients with pulmonary diseases.
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