Clario logo

Product Manager

Job Overview

Location

Costa Rica Remote

Job Type

Full-time

Category

Product Management

Date Posted

April 25, 2026

Full Job Description

đź“‹ Description

  • • As a Product Manager at Clario, you will play a critical role in shaping the future of medical imaging solutions by translating user and customer needs into impactful product strategies within a regulated environment that supports clinical trials, diagnostics, and medical decision-making.
  • • You will define and drive product vision and roadmap based on user needs, stakeholder input, and business priorities; gather, document, and prioritize product requirements through direct engagement with customers and cross-functional teams; collaborate with engineering to deliver product features, including contributing to requirements, UI concepts, and prototype reviews; monitor product performance using defined metrics and continuously improve quality and operational efficiency; and support sales and marketing efforts through product demonstrations, training materials, and market research.
  • • You will join a team at Clario, part of Thermo Fisher Scientific, dedicated to developing regulated technology that helps unlock better evidence and improve patient outcomes worldwide, working in a mission-driven organization focused on advancing clinical science and building innovative technology.
  • • In this role, you will develop expertise in medical imaging and clinical trial processes, strengthen your ability to influence cross-functional teams without formal authority, refine your product strategy and roadmap execution skills, and contribute directly to products that support life-changing therapies for patients globally.

Skills & Technologies

Product Management
Remote
Degree Required

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About Clario

Clario is a global healthcare technology and services company that provides endpoint data solutions for clinical trials. It delivers imaging, cardiac safety, respiratory, eCOA, and precision motion technologies, supported by scientific and regulatory expertise, to help biopharmaceutical sponsors generate high-quality evidence and accelerate drug development.

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