Clairo

Technical Product Manager

United Kingdom

Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, Life Sciences, Clinical Trials TechnologyIndustries

Job Description

Position Overview

Clario is seeking a Product Manager to align technical product plans with the overall portfolio and product vision. This role involves staying informed on new technologies, defining and maintaining a multi-year roadmap, and collaborating with technical teams to define architecture, user experience, and innovative features for clinical trial endpoint technology solutions.

About Clario

Clario is a 50+ year-old industry leader in delivering clinical trial endpoint technology solutions. Our innovative technologies are revolutionizing efficiency, accuracy, and integration of trial data, helping to unlock better clinical outcomes.

What We Offer

  • Competitive compensation
  • Attractive benefits (flexibility, support, and well-being)
  • Engaging employee programs
  • Remote working
  • Continual professional development

Responsibilities

  • Align 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.

Requirements

  • Education:
    • Bachelor's degree in business, science, technology, or medicine (required)
    • Master’s degree in Business Administration (preferred)
  • Experience:
    • 3+ years of experience in product management, ideally in healthcare or life sciences
    • Experience with full product lifecycle in clinical trials or healthcare
  • Skills & Knowledge:
    • 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

Employment Type

Full time

Location Type

Information not provided

Salary

Information not provided

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.

Skills

Product Management
Clinical Trials
Healthcare Technology
Roadmap Development
Architecture Design
User Experience
MVP Definition
Requirements Specification
Business Architecture
Product Lifecycle Management

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters
1972Year Founded
$29.9MTotal Funding
GROWTH_EQUITY_VCCompany Stage
Biotechnology, HealthcareIndustries
5,001-10,000Employees

Benefits

Competitive and equitable total rewards package
Physical, mental and financial health and wellness
Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.
The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.
AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.
The company has nearly 50 years of experience in clinical trial technology solutions.
Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.
The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.
Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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