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 Offer
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Competitive compensation
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Attractive benefits (flexibility, support and well-being)
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Engaging employee programs
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Remote working
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Continual professional development
What You’ll Be Doing
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Align technical product plans with the overall portfolio and product vision in partnership with Product Line Leaders and Upstream Product Managers.
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Stay informed on new technologies, industry direction, and market trends to inform product evolution.
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Define and maintain a multi-year roadmap, prioritizing initiatives and aligning them with product launch plans.
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Collaborate with technical teams to define architecture, user experience, and innovative features.
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Lead business architecture design including user and data workflows for assigned components.
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Work cross-functionally to validate concepts, define MVPs, and specify requirements.
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Balance technical maintenance, architectural integrity, and feature delivery.
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Support retrospectives and process improvements.
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Transfer knowledge to Product Owners and support internal enablement through documentation.
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Serve as subject matter expert to enable internal stakeholders and commercial teams.
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Lead release activities and support commercial launch readiness.
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May manage individual contributors.
What We Look For
Bachelor’s degree in business, science, technology, or medicine required; Master’s in Business Administration preferred. Candidates should have 3+ years of experience in product management, ideally in the healthcare or life sciences industry. The role requires:
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Experience in full product lifecycle within clinical trials or healthcare.
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Technical acumen with ability to translate business needs into technical requirements.
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Collaboration with UX/UI teams on workflow design.
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Domain-specific experience (based on assigned product line): Cardiac Safety/Respiratory: Medical device experience related to vital signs monitoring
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Knowledge of regulatory frameworks (e.g., FDA 510(k), CE marking, GCP, 21 CFR Part 11, MDR)
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Experience with Quality Management Systems and medical device lifecycle
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Understanding of GMP, GCP, and medical device security standards
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Proven ability to lead cross-functional teams and influence across all levels
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Strong decision-making in agile environments
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Excellent communication (written and verbal)
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Effective stakeholder management
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Strategic prioritization and focus alignment
Fluency in English required. Ability to travel up to 25%. This is a remote position based in the United Kingdom.
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.
