About Clario
Clario is a 50+ year-old industry leader in delivering clinical trial endpoint technology solutions. The future of clinical trials is evolving, and our innovative technologies are revolutionizing efficiency, accuracy, and integration of trial data. From new trial methodologies to faster, more integrated evidence collection, our solutions help unlock better clinical outcomes.
What We OfferCompetitive compensation
Attractive benefits (flexibility, support and well-being)
Engaging employee programs
Remote working
Continual professional development
What You'll Be DoingAlign technical product plans with the overall portfolio and product vision in partnership with Product Line Leaders and Upstream Product Managers.
Stay informed on new technologies, industry direction, and market trends to inform product evolution.
Define and maintain a multi-year roadmap, prioritizing initiatives and aligning them with product launch plans.
Collaborate with technical teams to define architecture, user experience, and innovative features.
Lead business architecture design including user and data workflows for assigned components.
Work cross-functionally to validate concepts, define MVPs, and specify requirements.
Balance technical maintenance, architectural integrity, and feature delivery.
Support retrospectives and process improvements.
Transfer knowledge to Product Owners and support internal enablement through documentation.
Serve as subject matter expert to enable internal stakeholders and commercial teams.
Lead release activities and support commercial launch readiness.
May manage individual contributors.
What We Look ForBachelor's degree in business, science, technology, or medicine (required)
Master's degree in Business Administration (preferred)
3+ years of experience in product management, ideally in healthcare or life sciences
Experience with full product lifecycle in clinical trials or healthcare
Strong technical acumen to translate business needs into technical solutions
Collaboration with UX/UI teams for workflow design
Domain expertise in Cardiac Safety/Respiratory: Experience with medical devices for vital signs monitoring
Familiarity with regulatory frameworks such as: FDA 510(k), CE Marking, GCP, 21 CFR Part 11, MDR
Experience with Quality Management Systems and medical device lifecycle
Knowledge of GMP, GCP, and medical device cybersecurity standards
Proven leadership of cross-functional teams and influence across levels
Agile decision-making and strategic prioritization
Strong communication skills (written and verbal)
Stakeholder management and business alignment
Fluency in English
EEO Statement
Clario is an equal opportunity employer. We evaluate all qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
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