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Barcelona, Catalunya, España
Remote only
Docplanner is a global healthcare platform connecting more than 300,000 doctors with approximately 100 million patients every month across 13 markets.
Within Docplanner, Noa is on a mission to help people live longer, healthier lives. We build AI that works alongside doctors to:
Remove their administrative work.
Help them make better decisions and handle repeatable cases, so they can spend their time where it matters most.
Help patients navigate healthcare using their medical history as personalized context.
We're already in doctors' hands: Noa Notes takes documentation off their plates, while Noa Evidence brings trustworthy medical evidence to the point of care.
The next frontier is the hardest—and the most valuable: helping doctors, and eventually patients, make decisions while our AI safely takes on repeatable clinical work. That's where a doctor's judgment has to live inside the product itself. That's this role.
You'll help take Noa from writing notes and providing evidence to helping doctors decide—and make sure that doctors and users trust it.
This isn't a traditional CMO, advisory or regulatory role. It's a hands-on clinical-product role: the clinician–product–AI. You'll do two things:
Help decide what we build for doctors by bringing their real needs, habits and workflows into the product.
Define the clinical quality of what we ship: what's correct, useful and safe, and make sure we can prove it.
Because you're a doctor yourself, you can talk to our users peer-to-peer and get the honest answers a survey never will. As our first dedicated clinical hire on the product, you'll set the approach, then help grow clinical expertise across Docplanner's AI product teams.
You'll work day-to-day with Product, AI, Design, Engineering, Regulatory and our doctor network.
Bring how doctors really work (habits, preferences, workflow, admin) into the product.
Talk to doctors, doctor-to-doctor, and turn candid feedback into product decisions.
Partner with Product on the roadmap: what to build and what will actually get used.
Define the clinical quality bar and intended outcomes for our AI products.
Review and improve prompts, model outputs, clinical templates, workflows and terminology.
Spot clinical failure modes: what good and unacceptable outputs look like.
Direct clinical evaluation: decide what to test, in what mix (specialty, population, complexity and edge cases), and set the bar. You'll bootstrap this with a dedicated owner who runs the process, tooling and annotation guidelines for doctors, while our clinical network performs the annotation.
Turn model errors and clinician feedback into concrete product and model improvements.
Work with ML/LLM teams, Regulatory experts and the PRRC to keep intent, evidence, risks and controls aligned, including EU MDR-related and similar requirements.
Build feedback loops with practising clinicians and our consultant-doctor network.
Define how clinical-product expertise scales across future products, teams and markets.
A medical degree and meaningful experience practising medicine, with a strong understanding of clinicians' day-to-day work. Active licensure and current clinical practice are not required, although recent or ongoing practice is valuable.
You've helped build and ship a digital health, clinical software or AI product—either within a product team or through meaningful entrepreneurial experience.
You've turned clinical problems into product decisions, not just provided advice or review.
Strong clinical judgment: you turn quality and safety into standards technical teams can use.
You win doctors' trust quickly—you are the peer who gets the honest answer.
You communicate clearly and directly across clinical, product, technical, regulatory and leadership teams.
You're comfortable working at a senior, hands-on level in a fast-moving, international team.
You actively use generative AI and understand its potential and limitations. Hands-on experience with prompting, evaluation, error analysis, human oversight or AI-assisted development tools such as Cursor and Claude Code is a plus.
Bonus: experience with ambient documentation, clinical templates, medical-knowledge systems, clinical coding, evaluation datasets or building and certifying regulated Software as a Medical Device (SaMD).
A clear clinical quality framework for our priority AI products.
Clinically grounded evaluation sets and thresholds in place.
A repeatable way to turn medical expertise into better product and model decisions.
Real impact at real scale: Your work reaches hundreds of thousands of doctors and their patients.
Shape what comes next: You'll influence what Noa and Docplanner's AI products become—and whether doctors and patients trust them.
Ship to learn: A feature in front of users beats another month of planning.
Work flexibly: The role is 100% remote within Poland or Spain, with the team coming together regularly.
