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About Lucis

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Requirements and qualifications

Clinical

What you will get

Benefits, compensation and workplace terms vary by location and are shown exactly as provided by Lucis on its official application page.

Lucis

Medical Director

📍 Paris, 💼 –+ years🏠 On-site◷ Full Time

About the role

Making preventive health the default for every human in Europe

The mission
At Lucis, we believe healthcare should be preventive, not reactive. We’re building the operating system for human longevity to help people add more healthy years to their lives.

The role
Lucis analyses 110+ biomarkers, builds personalised clinical protocols, and delivers them through an AI-powered preventive health product. We are live in France and opening the UK, Portugal and Spain.
This role exists to turn clinical judgement into the medical standards the company can run on.
We are hiring a Medical Director to own Lucis's clinical direction and medical safety system.

You will:
Decide what we test and why, and to what clinical standard the service runs

Set the risk posture and the governance model: who signs what, how incidents are handled, what Lucis can claim

Own the certification call and path: medical device classification, CE, ISO, or stay out of scope, and the argument behind it

Hire and lead the clinical operations and safety team.

Represent Lucis clinically with labs, insurers, institutional partners and regulators, alongside the CMO

Set the standards that product team should follow to make each release safe.

About you
You're passionate about the future of human health and want your work to help people stay healthy for longer. You move quickly from idea to execution, take full ownership of what you build, and work best with talented people who care as much as you do.
You thrive in fast-moving environments, learn by doing, and value feedback as a way to continuously improve.

You'll fit in well if
Have an MD and roughly 5 to 10 years of hospital practice

Have led people and systems since, in healthtech, diagnostics, pharmaceutical company as medical affairs or CRO

Have held a quality or regulatory seat, and can carry a certification decision rather than hand it to a consultant

Can set a standards and orchestrate other doctors to execute your vision

Are fluent in French and English, spoken and written

Use AI in your daily work and can explain when it fails and what you do about it

We might not be a fit if
You want to focus primarily on traditional bedside practice

You prefer pure research or citation work without shipping clinical standards

You are a copywriter without real clinical practice

You need every process already defined before you contribute

You prioritise predictable nine-to-five work over mission intensity

Practical details
Format: Full-time preferred. Flexible for the right senior profile.

Location: Paris mostly

Languages: French and English required. Additional language a plus.

The process
Introductory call (20 minutes)

Technical interview (30–60 minutes) — clinical judgement, protocol/evidence thinking, writing sample or case

At-home case study (within two days)

Deep dive and team conversations in Paris

Reference calls

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Requirements

  • Clinical

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