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product management documentation regulatory affairs healthcare user interviews📋 Description
- Own the Oncology Provider Portal for Japan and scale key product lines.
- Lead cross-functional teams across business, regulatory, engineering, design.
- Gather insights via user interviews; convert to BRD/PRD and user stories.
- Define acceptance criteria; drive the Japan product roadmap.
- Build country-wide user experiences impacting millions of patients.
- Communicate roadmap and secure senior stakeholder alignment.
🎯 Requirements
- Japanese fluency in language, culture, and regulation.
- 3-5+ years in software product management (digital health/biotech).
- Experience with regulated products and regulatory affairs.
- End-to-end product development experience.
- Excellent communication, facilitation, and analytics.
- Strong cross-functional leadership and systems thinking.
- User-centric, empathetic problem solver with integrity.
- Willingness to travel to Japan 1-2x per year.
🎁 Benefits
- Medical, dental, vision, life and disability plans.
- Fertility care benefits.
- Pregnancy and baby bonding leave.
- 401k benefits and commuter benefits.
- Employee referral program.
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