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C

Technical Product Lead – Regulatory Innovation

Cpl Life Sciences City of London
new


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    C

    Technical Product Lead – Regulatory Innovation

    Cpl Life Sciences City of London
    new
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Salary

    Job description

    • Technical Product Lead – Regulatory Innovation
    • London, UK - Hybrid


    We are seeking a hands-on, execution-focused Technical Product Lead – Regulatory Innovation to operate at the intersection of AI product development, clinical research, and regulatory strategy.

    This role is ideal for individuals with a technical foundation in AI/ML or software engineering who have evolved into product and regulatory leadership within life sciences.


    You will drive the development of fit-for-purpose, regulator-ready AI solutions used in clinical trials and clinical practice. A key focus will be enabling lean, scalable processes while advancing regulatory acceptance of novel AI methodologies.


    You will work cross-functionally across product, engineering, data science, clinical, and quality teams, and collaborate closely with regulatory stakeholders.


    Key Responsibilities

    1. Lean Quality & Process Enablement

    • Partner with Quality to ensure the Quality Management System (QMS) is scalable, efficient, and minimally burdensome
    • Embed quality and compliance into developer-native workflows
    • Eliminate or refine controls that do not materially reduce risk
    • Support teams in computerised system validation (CSV) from requirements definition through to validation and acceptance
    • Provide pragmatic guidance, templates, and training on regulatory expectations without becoming documentation-driven
    • Contribute to alignment across QMS, information security, and internal governance frameworks


    2. Regulatory Innovation & Strategy

    • Monitor and interpret the evolving regulatory landscape for AI in healthcare and clinical trials
    • Identify opportunities to apply innovative AI approaches within regulatory frameworks
    • Translate internal innovations into regulator-ready evidence packages and methodologies
    • Support and participate in regulatory engagement activities (e.g., scientific advice, workshops, industry forums)
    • Contribute to shaping emerging standards and expectations for AI validation and deployment


    3. Product Leadership

    • Translate user needs, regulatory requirements, and scientific insights into clear product requirements and acceptance criteria
    • Collaborate with engineering, data science, and clinical teams to define and prioritise the product roadmap
    • Own the end-to-end product lifecycle, ensuring alignment across commercial, scientific, and regulatory objectives
    • Define and manage stage-gates to ensure readiness for validation, release, and scaling
    • Track product performance and user outcomes, driving continuous improvement


    Required Skills & Experience

    • Degree in Engineering, Computer Science, or a related technical discipline
    • Significant experience in product ownership and regulatory environments, ideally within:
    • AI-enabled healthcare software
    • Clinical trial systems
    • Regulated digital products
    • Strong understanding of quality, validation, and regulatory frameworks, such as:
    • GxP / ICH-GCP
    • Computerised system validation (CSV / GAMP 5)
    • ISO standards (e.g., 13485, 14971, 62304)
    • Data integrity and electronic records requirements
    • Familiarity with emerging guidance on AI/ML in healthcare, including risk management and governance frameworks
    • Proven ability to design lean, scalable processes that support high-velocity product delivery in regulated environments
    • Technical fluency in AI/ML concepts, system architecture, and data pipelines
    • Strong analytical thinking and problem-solving skills
    • Ability to operate in cross-functional, fast-paced environments with a high degree of ownership


    Preferred Experience

    • Experience within clinical trials (sponsor, CRO, or technology provider)
    • Exposure to regulatory interactions, submissions, or advisory processes
    • Experience contributing to novel regulatory approaches or frameworks
    • Knowledge of information security standards (e.g., ISO 27001, SOC 2)
    • Experience supporting regulated product submissions (e.g., CE marking, FDA pathways)


    What We’re Looking For

    • A hybrid thinker who can bridge technology, product, and regulation
    • A pragmatic, detail-oriented operator who prioritises execution over theory
    • Someone who challenges complexity and drives lean, outcome-focused processes
    • A confident communicator capable of engaging both technical teams and external stakeholders


    Working Environment

    • Cross-functional, collaborative environment at the intersection of AI and life sciences
    • Opportunity to contribute to cutting-edge innovation in clinical research and healthcare
    • Hybrid working model (location flexible depending on organisation)

    About the employer

    Cpl Life Sciences
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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