Key skills
Leadership
About this role
Role Overview
- Leading HIV-focused regulatory writing activities
- Managing program-level writing efforts
- Partnering with clinical and regulatory teams
- Overseeing projects that span multiple products
- Providing key contributions to clinical strategy
Requirements
- PhD or PharmD or MPH or MS
- Lead-author experience on regulatory submissions
- Infectious disease experience
- Matrix leadership experience
Benefits
- Health insurance
- 401(k) matching
- Flexible work arrangements
- Professional development
- Benefits offered by GSK