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, 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.
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What We Do
-- Clario has been named a Top Workplace by Energage for the 2022 Top Workplaces USA national awards. -- Clario generates the richest clinical evidence by fusing our deep scientific expertise and global scale into the broadest endpoint technology platform. By doing this, we empower our partners to transform lives. With almost 50 years of experience, 19,000 clinical trials, and 870 regulatory approvals, Clario has mastered the ability to generate rich evidence across a Trial Anywhere™ portfolio: decentralized (DCT), hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe, and Asia Pacific, Clario delivers the power of certainty. Partners ————— Clario brings the best of ERT and Bioclinica together to work alongside our partners to solve some of their biggest questions on topics such as: - eCOA vs. paper - Decentralized Clinical Trial (DCT) - Rescue a clinical trial - Broad endpoint technology: cardiac safety, imaging, respiratory And many more. People ———— We are so honoured to be named a 2022 Top Workplace by Energage. One of our leading values at Clario is People First Always. We help individuals build meaningful careers at Clario as they serve to help transform patients lives. Join us on this journey and check out our careers page: https://clario.com/careers/
