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Clario Holdings Inc.

Technical Product Manager (f/m/x)

Clario Holdings Inc., New Bremen, Ohio, United States

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Technical Product Manager (f/m/x) page is loaded## Technical Product Manager (f/m/x)locations:

Estenfeld, Germany:

Leuven, Belgium:

United Kingdom Remotetime type:

Full timeposted on:

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R16674Clario is hiring a **Technical Product Manager (f/m/x)** to drive innovative, data-driven products that improve patient outcomes and accelerate research. If you bring technical depth, product vision, and a passion for transforming healthcare through technology - this is your opportunity to make a meaningful impact.**What we offer*** Competitive compensation* Flexible work schedules* Attractive PTO plan* Engaging employee programs**What you'll be doing*** Align product roadmaps with overall vision in partnership with Product Line Leaders and Upstream Product Managers* Monitor emerging technologies and industry trends to inform strategy* Develop and maintain multi-year release plans and initiatives* Collaborate with technical teams on architecture, UX, and key capabilities* Lead business architecture and workflows for assigned product areas* Validate concepts and requirements through stakeholder feedback* Balance priorities across architecture, maintenance, and new features* Support agile ceremonies and team retrospectives* Partner with Product Owners to ensure accurate knowledge transfer* Act as subject matter expert in cross-functional initiatives* Contribute to internal knowledge bases and user documentation* Lead release readiness and commercial launch activities* May manage individual contributors**What we look for*** Bachelor’s degree in business, science, technology, or medicine (Master’s in Business Administration preferred)* 3+ years of product management experience, ideally in healthcare or clinical trials* Strong technical acumen and ability to communicate across teams* Full product lifecycle experience and domain knowledge in life sciences* Proven collaboration with UX/UI teams on business and data workflows* Excellent prioritization and decision-making in agile environments* Strong customer engagement and communication skills* Leadership experience with ability to influence across levels* Experience with respiratory or clinical data capture technologies* Experience developing specs within a Quality Management System* Familiarity with FDA 510(k), CE Marking, and global device approvals* Understanding of GCP, 21 CFR Part 11, device security, GMP, MDD, MDRAt Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.Experience in Respiratory medical device hardware and software development would be beneficial.Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints.For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015. #J-18808-Ljbffr