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Associate Principal - COAA Scientific AI Lead - UK and EU (home-based or hybrid)

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United Kingdom
Work type
Hybrid
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This role is available in the UK and in the European Union. The list of countries in the job ad is not exhaustive.


Associate Principal, COAA Scientific AI Lead

IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. Our Clinical Outcomes Assessments (COAs) organisation leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialisation of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our clients – mostly life science/pharmaceutical companies – through the application of broad consulting expertise and technical scientific knowledge to conduct scientifically rigorous research. This research is broad and includes qualitative, quantitative, and passive approaches to understand patient, caregiver, and healthcare professional experiences and expectations of disease and treatment.


The COA Accelerator ecosystem is expanding its AI-enabled product capabilities to help internal teams and external clients develop evidence-backed COA strategies more efficiently, consistently, and transparently. These capabilities are intended to support workflows such as therapy area and indication review, COA instrument selection, endpoint strategy, regulatory precedent assessment, psychometric evidence review, source-backed rationale development, expert review, and report generation.


To meet our client expectations and retain the excellent reputation built up over time, the IQVIA COAs team is committed to recruiting, training and supporting driven individuals who have life science, consulting, product management, AI product, and/or clinical technology skills that can be applied to COA research and technology-enabled offerings. Individuals joining us are assured of a rewarding and progressive career in patient-focused research.


You’ll have the opportunity to address challenging client issues, across multiple geographies, with a hands-on influence in developing and delivering innovative solutions. We operate in a truly multi-cultural, collegial and collaborative work environment that is rich in development and growth.

Role & Responsibilities

  • Own the product vision, roadmap, prioritisation, and lifecycle management for AI-enabled COA selection and COA Accelerator capabilities.
  • Translate the strategic concepts into practical product capabilities, user journeys, workflows, release milestones, and measurable success criteria.
  • Define the product’s target users, use cases, workflows, outputs, quality standards, adoption needs, and commercial value proposition across internal and external use cases.
  • Prioritise product capabilities across AI instrument analysis and selection, evidence retrieval, source citation, insight generation, endpoint review, assessment schedule design, regulatory considerations, expert review, and report generation.
  • Work with COA scientists, HEOR experts, strategy consultants, study teams, sponsors, commercial stakeholders, and clients to understand how COA selection is currently performed and where AI-enabled workflows can add value.
  • Define product requirements for user inputs such as therapy area, indication, target product profile, mechanism of action, study phase, target population, endpoint objectives, geography, regulatory pathway, and intended use.
  • Define expected product outputs, including COA insights, endpoint review, assessment schedule, rationale, evidence gaps, regulatory insights, payer inisights, and source-backed recommendations.
  • Ensure product requirements are specific enough for engineering delivery while preserving the nuance needed for expert scientific judgement.
  • Partner with AI engineers and COA experts to define quality criteria for AI-generated outputs, including factuality, retrieval relevance, citation accuracy, clinical usefulness, consistency, and escalation triggers.
  • Create workflows for expert review, feedback capture, error analysis, model improvement, quality monitoring, and continuous product refinement.
  • Ensure the product clearly distinguishes between evidence-backed insigts, expert inference, precedent-based assumptions, and areas of uncertainty.
  • Partner with data engineering and domain experts to prioritise the knowledge sources required to power the product, including COA libraries, instrument metadata, psychometrics, clinical trial records, labels, HTA documents, regulatory correspondence, and scientific literature.
  • Define metadata, traceability, citation, and source inspection requirements from a product and user perspective.
  • Serve as a product-facing point of contact for internal stakeholders and selected client-facing discussions related to COA insights and selection AI capabilities.
  • Support demos, prototypes, pilots, business cases, training materials, internal enablement, onboarding workflows, and adoption planning.
  • Work with Commercial and Strategy teams to define product positioning, packaging, differentiation, value story, and integration with broader COA Accelerator.
  • Lead cross-functional delivery across AI Engineering, Data Engineering, Software Engineering, COA Science, UX, Security, Legal, Compliance, Commercial, and client-facing teams.
  • Own backlog prioritisation, requirements definition, sprint planning input, acceptance criteria, release readiness, stakeholder communication, and product decision documentation.

Skills & Qualifications

  • Degree in life sciences, health outcomes, clinical research, public health, biomedical sciences, data science, product management, technology, or a related field.
  • Experience in COA strategy consulting, HEOR consulting, clinical outcomes research, eCOA, clinical trial technology, regulatory strategy, patient experience research, or medical evidence generation.
  • Ability to translate complex workflows into product requirements, user journeys, and delivery plans.
  • Strong stakeholder management skills, including ability to work with scientific experts, senior leaders, commercial teams, client-facing stakeholders, and technical contributors.
  • Ability to balance scientific rigour, user needs, commercial value, technical feasibility, governance requirements, and delivery constraints.
  • Strong written and verbal communication skills, including ability to create clear product narratives, requirements, executive materials, demos, and client-facing explanations.
  • Strong prioritisation skills and ability to make pragmatic trade-off decisions in ambiguous, evolving, and regulated environments.
  • Ability to work independently in a remote or hybrid environment while collaborating across global teams.

Additional Requirements

  • Experience with AI-enabled products, LLM applications, retrieval-augmented generation, knowledge management platforms, evidence synthesis tools, or clinical decision-support products is preferred.
  • Experience in product management, AI product management, data product management, digital health, clinical technology, life sciences software, SaaS platforms, or technology enabled consulting offerings is preferred.
  • Experience working with proprietary content, licensed data, regulated content, client-specific knowledge repositories, or permissioned knowledge spaces.
  • Experience with product discovery, prototyping, pilot design, user testing, go-to-market support, and customer adoption planning.
  • Experience or willingness to build products for both internal enterprise users and external client users.
  • Ability to analyse usage data, client feedback, adoption metrics, and qualitative insights to inform product direction.
  • Comfort with virtual collaboration, training, demo, and client engagement tools such as Teams, Zoom, PowerPoint, whiteboarding tools, and product management platforms.
  • Significant experience leveraging AI tools for work.
  • Fluency in English.

Please submit your CV in English.

Please note we don't sponsor visa.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

About Us

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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