Hiring.Camp

Principal Product Manager, Acute Care CT

DeepHealth

·

1 week ago

Salary
€70k – €80k
Location
Paris, Île-de-France, France
Workplace
Hybrid
Type
Full-time
Department
Business and Product
Seniority
Senior
Education
Bachelor
Source
Recruitee

Description

The Principal Product Manager, Acute Care CT owns the DeepHealth Acute Care CT Suite end to end, with primary accountability for what to build and shared accountability for getting it shipped. DeepHealth is building the Acute Care CT Suite from the ground up to cover detection, care coordination, and reporting for emergency CT, starting with head CT and expanding to chest and abdomen, where minutes saved in stroke, bleeds, and trauma directly affect patient outcomes. The Principal Product Manager, Acute Care CT shapes the suite from day one: owning the roadmap, translating clinical needs into ML and product work, and driving cross-functional delivery on a subset of the suite from data through customer activation. The role does not write code or own technical software design.

Essential Duties and Responsibilities

Product Strategy and Roadmap

  • Own the Acute Care CT Suite roadmap and define what to build, defer, or stop based on evidence.

  • Define suite scope across pathology detection modules, software capabilities such as alerting and care coordination, and comprehensive draft reporting.

  • Work with emergency radiologists and neuro/stroke teams to distinguish stated requests from real clinical needs, including time-to-treatment, triage, missed findings, and care coordination.

  • Translate clinical problems into ML work and set model metrics that reflect clinical value, including sensitivity versus false-positive burden.

  • Track the acute care market (including Aidoc, Viz.ai, RapidAI, Nicolab, and peers) and position products with Sales and Marketing.

  • Delivery and Cross-Functional Execution

  • Own delivery end to end on a subset of the Suite, from data to customer activation, including planning, coordination across data, ML, software, QARA, and Support, tracking, and escalation.

  • Run squads for new devices (typically 3 to 9 months), such as ASPECTS detection.

  • Coordinate with QARA on the regulatory impact of each release, including EU MDR and FDA 510(k).

  • Cut scope or move dates when needed, and escalate further as required.

  • Partner with engineering and technical leads without writing code or carrying technical software design.

PLEASE NOTE: This is not an exhaustive list of all duties, responsibilities and requirements of the position described above. Other functions may be assigned and management retains the right to add or change duties at any time.

Skills

Machine LearningFDACompliance

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