Director of Special Projects & International Growth
Quick Summary
building for the most demanding regulatory bar in each new market before entry. Own end-to-end operational readine
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eMed is redefining the future of at-home care, leveraging physical and digital technologies to cut costs, increase capacity, and improve quality of care. We're building the complete chronic condition management platform that lets patients manage chronic conditions from home, safely and at scale. Our flagship focus today is GLP-1 weight management delivered at scale, with SheMed (women-focused) and HeMed as related brands. We're an NHS partner in the UK and are actively expanding into new international markets. We're looking for a senior operator who can work directly alongside the Managing Director, moving fluidly between whatever the highest-priority problem is; right now, that's standing up a UK B2B/employer channel and driving international market readiness, but the role is deliberately built to flex as priorities shift. This is a senior, high-autonomy role for someone who acts as a direct extension of the Managing Director, picking up whatever needs serious ownership, wherever it sits. Right now the two biggest priorities are:
The mandate isn't fixed to these two areas. You should expect the scope to shift toward whatever's most urgent. This role suits someone who wants broad ownership and variety, not a narrowly defined lane. |
Responsibilities
~1 min read- Assist with building and scaling the UK employer/B2B proposition, building on eMed's existing capitation pricing model and market positioning
- Develop and execute a go-to-market strategy covering brokers, insurers, and direct employer relationships
- Drive eMed's regulatory-first market-entry approach: building for the most demanding regulatory bar in each new market before entry.
- Own end-to-end operational readiness tracking across all international markets: regulatory approval, partner agreements, incorporation, and launch readiness
- Manage relationships with in-market Country Managers, and lead onboarding for new markets as they come online
- Coordinate cross-functional workstreams spanning regulatory approval, clinical partnerships, pharmacy and lab logistics
- Identify, escalate, and resolve blockers to market entry (device approvals, care-model regulatory constraints, partner sourcing gaps)
- Report readiness status and progress regularly to the leadership team, with a clear view of what's blocking each market from launch
- Take direct ownership of high-priority initiatives as they arise, spanning commercial, operational, or strategic work
- Act as a trusted senior deputy to the Managing Director, able to represent them in partner, regulatory, and internal discussions
- Move between workstreams as priorities shift, without needing extensive ramp-up time
- Present regular updates to leadership and the board across whichever priorities are live at the time
- Build and lead a small team as specific workstreams scale
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Nice to Have
~1 min read- Existing relationships with UK employer benefits brokers or insurers
- Experience working with healthcare regulators
What We Offer
~2 min readLocation & Eligibility
Listing Details
- Posted
- July 17, 2026
- First seen
- July 17, 2026
- Last seen
- July 18, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 54%
- Scored at
- July 17, 2026
Signal breakdown
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