Full-Time

Senior Product Manager 2

ClinicalKey Nursing

Updated on 9/12/2026

RELX

RELX

1,001-5,000 employees

Global information analytics and decision tools

Compensation Overview

$115.4k - $192.3k/yr

+ Annual incentive bonus

Company Historically Provides H1B Sponsorship

Pennsylvania, USA + 1 more

More locations: Oregon, USA

In Person

Bachelor's, Master's

Category
Product (1)
Required Skills
Product Management

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Requirements
  • 10 years of experience delivering customer-facing Software as a Service or enterprise software products, with 8+ years of product management experience, including ownership of complex cross-functional initiatives.
  • Experience building or managing platform products, integrated product experiences, or enterprise software ecosystems.
  • Demonstrated ability to think strategically across multiple products while balancing customer needs, technical considerations, and business priorities.
  • Strong technical acumen, including experience working with application programming interfaces, integrations, authentication, and modern application architectures.
  • Exceptional customer discovery and user research skills, with a focus on understanding customer workflows and translating insights into product strategy.
  • Proven ability to influence cross-functional teams and build alignment across multiple product organizations.
  • Strong analytical skills with experience using product metrics and customer insights to drive decision making.
  • Bachelor's or Master's degree in a relevant discipline.
Responsibilities
  • Collaborate with the Vice President of Product and other product leaders on strategic vision, informed by customer research, product analytics, and market insights.
  • Create and execute a roadmap to create a cohesive and intuitive experience across multiple products, in partnership with other product managers across the nursing portfolio.
  • Define platform capabilities that improve navigation, discoverability, personalization, administration, reporting, and overall usability across the Nursing ecosystem.
  • Prototype and validate cross-product concepts quickly, using customer feedback, artificial intelligence-assisted tools, and iterative experimentation to refine product direction before development.
  • Collaborate with engineering and platform product managers to define platform architecture, including application programming interfaces, authentication, shared services, and modular user interfaces that enable products to work together effectively.
  • Lead artificial intelligence-first, specification-driven product development by translating customer needs, workflows, and business objectives into clear product specifications that guide design, engineering, testing, and delivery.
  • Partner closely with engineering, user experience, and artificial intelligence development teams to iteratively refine specifications, validate assumptions through rapid experimentation, and ensure solutions meet customer needs before implementation.
  • Serve as an advocate for nursing customers, ensuring product decisions reflect real-world workflows and customer needs.
  • Use customer insights, product analytics, and market trends to prioritize investments and guide roadmap decisions.
  • Partner with user experience, engineering, clinical, commercial, and content teams to deliver high-quality, scalable experiences that ensure alignment with customer needs, product excellence, regulatory compliance, and successful market delivery.
  • Define success metrics and continuously evaluate ecosystem performance to proactively improve adoption, engagement, and customer satisfaction.
Desired Qualifications
  • Strong understanding of healthcare technology, clinical workflows, learning platforms, or education technology.
  • Experience working within artificial intelligence-assisted software development environments, using structured specifications to guide engineering, testing, and delivery.
  • Experience in healthcare technology, enterprise software, or education technology.
  • Master's degree in a technical subject, such as Computer Science or an Engineering discipline.

RELX is a global provider of information-based analytics and decision tools for professionals across scientific, technical, medical, legal, risk, business, and exhibitions industries. It operates in four segments: Scientific, Technical & Medical; Risk & Business Analytics; Legal; and Exhibitions. Its products combine large datasets, analytics, and decision-support tools to help researchers, healthcare professionals, lawyers, and business leaders make informed choices, improve productivity, and achieve better outcomes. Revenue mainly comes from subscriptions, with additional income from transactional sales and advertising. RELX differentiates itself through its deep data assets, specialized industry knowledge, and multi-segment offerings that span content, analytics, and decision-support services. The company pursues a goal of delivering trusted information and insights while supporting corporate responsibility and alignment with the UN SDGs through its products and partnerships.

Company Size

1,001-5,000

Company Stage

IPO

Headquarters

London, United Kingdom

Founded

1894

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Simplify Jobs

Simplify's Take

What believers are saying

  • H1 2026 revenue grew 7%; Legal grew 10%; Risk grew 8%.
  • February 24, 2026 Lexis+ with Protégé launched globally, expanding AI workflow adoption.
  • September 3, 2026 Doctrine closes, targeting one million European legal professionals.

What critics are saying

  • Anthropic and Thomson Reuters compressed legal AI pricing after February 2026 market shock.
  • Harvey and Legora court law schools in 2026, training future buyer cohorts elsewhere.
  • Exhibitions face Middle East event uncertainty through 2026, threatening margins and calendar-dependent cash flows.

What makes RELX unique

  • LexisNexis’ 200 billion-document corpus still beats generic legal AI models.
  • September 3, 2026 Doctrine acquisition deepens RELX’s European legal AI workflow moat.
  • H1 2026 subscriptions supplied 62% of revenue, stabilizing cash generation.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401(k) Retirement Plan

401(k) Company Match

Wellness Program

Mental Health Support

Family Planning Benefits

Health Savings Account/Flexible Spending Account

Flexible Work Hours

Remote Work Options

Company News

Citybiz
Apr 28th, 2026
RELX to Acquire Legaltech Platform Doctrine in European AI Push

RELX Group has entered into an agreement to acquire French legal technology company Doctrine, a move that would expand its... Read More

Business Insider
Mar 1st, 2026
LexisNexis CEO dismisses AI threat as company reports 7% revenue growth

LexisNexis CEO Sean Fitzpatrick has dismissed investor concerns that AI threatens the legal software giant, saying proprietary data gives it a competitive advantage. Shares of parent company Relx fell 14% on 3 February following Anthropic's launch of an AI agent that drafts legal briefs, and are down 17% year-to-date. Fitzpatrick said LexisNexis's database of 200 billion legal documents, including content from Shepard's Citations dating to 1873, cannot be replicated by AI model makers. The company doesn't license its proprietary data to general-purpose AI providers. Relx reported 7% revenue growth for 2025 and 9% increase in adjusted operating profit, driven by customers adopting AI tools. LexisNexis is hiring and hasn't conducted AI-related redundancies.

Yahoo Finance
Feb 22nd, 2026
RELX's LexisNexis launches AI-powered identity management platform for healthcare

LexisNexis Risk Solutions, a wholly owned subsidiary of RELX, has launched a new identity management platform for the healthcare sector. Announced on 19 February, the tool combines identity verification, matching and enrichment capabilities with AI-powered authentication to enhance security throughout patients' healthcare journeys. The platform integrates LexisNexis IDVerse and offers enhanced identity verification, resolution and fraud protection. For healthcare professionals, it accelerates onboarding processes, automates processing and provides digital checks to prevent fraud. RELX is a global information and analytics company serving professional and business customers across scientific, technical, medical, legal and risk management markets.

PR Newswire
Jun 4th, 2025
Elsevier Unveils Rigorous Evaluation Framework To Mitigate Risk In Generative Ai Clinical Decision Support Tools

Clinician-centered framework will be featured in upcoming issue of the Open AccessJournal of the American Medical Informatics Association (JAMIA)Initial evaluations of ClinicalKey AI show high accuracy and usefulness in responses amongst cliniciansNEW YORK, June 4, 2025 /PRNewswire/ -- Elsevier, a global leader in medical information and data analytics, unveiled a groundbreaking evaluation framework for assessing the performance and safety of generative AI-powered clinical reference tools. This innovative approach has been developed for all Elsevier Health generative AI solutions, including ClinicalKey AI, Elsevier's advanced clinical decision support platform, and sets a new standard for responsible AI integration in healthcare. It will be featured in a future issue of the Open Access Journal of the American Medical Informatics Association (JAMIA).The framework, designed with input from clinical subject matter experts across multiple specialties, evaluates AI-generated responses along five critical dimensions: query comprehension, response helpfulness, correctness, completeness, and potential for clinical harm. It serves as a comprehensive assessment to ensure that AI-powered tools not only provide accurate and relevant information but also align with the practical and current needs of healthcare professionals at the point of care.Omry Bigger, President of Clinical Solutions at Elsevier: "This evaluation framework not only supports innovation and advancements to improve patient care but adds an extra layer of review and assessment to ensure physicians are armed with the most accurate information possible. It's a critical step in the implementation of responsible AI for healthcare providers and patients."In a recent evaluation study of ClinicalKey AI, Elsevier worked with a panel of 41-board certified physicians and clinical pharmacists to rigorously test responses generated by the tool for a diverse set of clinical queries. That panel evaluated 426 query-response pairs, and results demonstrated impressive performance, with 94.4% of responses rated as helpful, 95.5% assessed as completely correct, with just 0.47% flagged for potential improvements.Leah Livingston, Director of Generative AI Evaluation for Health Markets at Elsevier, said: "These results reflect not just strong performance, but the real value of bringing clinicians into the evaluation process

PharmiWeb
May 7th, 2025
Elsevier Adds Half A Million Records From Clinicaltrials.Gov To Embase, Enabling A Seamless Search Experience In The World’S Most Comprehensive Biomedical Database

London, 6 May 2025 – Elsevier, a global leader in information and analytics, is announcing the addition of half a million records from ClinicalTrials.gov to its leading biomedical literature database, Embase. The integration will enable researchers to seamlessly view high-quality information on clinical research studies and their results alongside the peer-reviewed literature, in-press publications and conference abstracts already available in Embase. Researchers will be able to conduct more comprehensive evidence and literature searches while having the confidence they will never miss important updates relevant to their drug, therapy, or medical device. Clinical trials data is a vital component of biomedical literature search, helping pharmaceutical and medical device companies stay informed about the latest scientific advancements, regulatory requirements, and competitive insights to support evidence-based decision-making. However, gathering data from multiple sources is currently prone to errors and is time-consuming, such as the duplication of search results, which slows research and regulatory processes. As new therapies and devices are developed and RD organizations seek collaborative partners, they must undertake thorough searches and justifications of evidence