Medical Director

Status
Open
Remote policy
Not stated
Employment type
Full-time
Salary
Not stated
Categories
Clinical
Tech
manager
Source
arbeitnow
First observed
2026-11-03 04:46 UTC
Last seen
2026-11-03 04:46 UTC
Source claims posted
2026-11-03 03:40 UTC
Consecutive misses
0 of 3

What the posting says

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

Quality

Completeness: 45%

Not enough history yet to judge honesty signals.

Timeline

  1. *
    #1700651 2026-11-03 04:46 UTC
    Published