Technical Product Manager (f/m/x)

Overview

Are you ready to lead the development of next-generation clinical trial solutions? Clario 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, MDR

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It's only through our people that we can continue to innovate technology that will shape the future of clinical trials.