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Lucis analyse les biomarqueurs sanguins et fournit des recommandations personnalisées via une application. La plateforme aide les utilisateurs à comprendre leur santé et à agir de façon préventive.

Repères sur Lucis
Secteur
Santé, pharmacie et biotech
Modèle
B2C
Type d’entreprise
Financée par du capital-risque
Stade
Startup early-stage
Siège
Paris
Domaine officiel
lucis.life
Effectif public
20 employés
Financement total publié
28 M$Source ↗
Dernière levée
Série A · 2026-05-01
Montant annoncé
20 000 000 $
Offres ouvertes
11

Investisseurs mentionnés

Détails de l’offre

La description complète publiée par Lucis.

Voir l’offre originale ↗

Description de l’offre

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 more than 110 biomarkers, builds personalised clinical protocols, and delivers them through an AI-powered preventive health product. As Medical Excellence, you are the senior medical expert next to product and Medical ops. You bring deep clinical expertise into protocols, ranges, evidence, and what we can say next to a marker. You also cover medical content: biomarker copy, protocols, and marketing clinical sign-off. You work with the product lead, Medical ops, medical reviewers, and AI.

You do not own product decisions, and you do not own labs, partners, or turnaround — Medical ops does. This is not a traditional bedside role. It is not an ops role. It is not a copywriting role. You have practiced medicine in depth, and you can turn clinical judgment into clear protocols, ranges, and member-facing language.

What you own protocols & clinical standards

Protocol logic, decision trees, clinical rules

  • Biomarker thresholds and expert ranges
  • Translate medical reasoning into structures the product and Medical ops can run
  • Keep protocols aligned with current evidence
  • Support new biomarkers, health systems, and preventive programmes from the clinical side

Evidence & clinical judgment

Evidence bar: what we should test, drop, or claim

  • Brief product and the team without a 40-page memo
  • Clinical review of edge cases and sensitive outputs
  • Review of AI-generated medical outputs for clinical accuracy and safety

Medical content

Biomarker explanations, protocol rationales, in-product clinical language

  • Coach / member-facing clinical copy
  • Marketing clinical sign-off
  • French and English at publication quality
  • Keep member-facing clinical language trustworthy

Medical quality and governance

Clinical review and sign-off processes (clinical side: what must be medically signed off, and to what standard)

  • Quality-control systems, documentation standards, audit trails
  • in partnership with Medical ops
  • Escalation and medical risk-management processes
  • clinical criteria and judgment
  • Clinical performance indicators
  • definition of medical quality bars, with Medical ops on measurement and ops

About you

  • You are a doctor with substantial clinical practice.
  • You care that what members read and what protocols encode is medically sound.
  • You are comfortable working with product and AI without needing to run either.
  • You write like a clinician people would trust.

You’ll fit in well if

You hold an MD (preferred) with deep clinical practice

  • more experience than a junior reviewer
  • Prevention, internal medicine, nutrition, functional, cardiology, public health, or a related field is a plus
  • You have strong clinical judgement, case by case and when defining standards
  • You can set protocol logic, ranges, and an evidence bar other people can execute
  • You write clearly in French and English at publication quality
  • You work well with product, Medical ops, AI, and reviewers
  • without owning their roadmaps
  • You balance medical rigour with pragmatism
  • You take ownership beyond a narrow specialty lane WE MIGHT NOT BE A FIT IF
  • You want to focus primarily on traditional bedside practice
  • You want to run labs, partners, turnaround, or ops queues (that’s Medical ops)
  • You want to own the product roadmap
  • 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 / Europe
  • Languages: French and English required. Additional language a plus.
  • Relocation support possible. Europe-based candidates welcome if willing to travel regularly to Paris.

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

Prérequis

  • MD preferred
  • Deep clinical practice
  • Strong clinical judgement
  • Publication-quality writing in French and English

Avantages mentionnés

  • Relocation support possible

Lieu de travail

Adresse confirmée

L’offre publie directement cette adresse.

156 Rue Oberkampf, 75011 Paris
Indice de confiance 5 sur 5
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