Director Product Portfolio - Life Sciences

Role Summary

LexisNexis is seeking a Director, Product Portfolio – Life Sciences to lead portfolio strategy, investment planning, and product execution across our Life Sciences business. This leader will help shape the future of a next-generation regulatory intelligence, data management, workflow, and submission platform that enables customers to move faster, stay compliant, and operate with greater confidence across global markets.

About the role

This is not a single-product role. It is a portfolio leadership role for an experienced product executive who can connect customer outcomes, portfolio choices, platform strategy, and commercial impact.

Responsibilities

• Lead the Life Sciences product portfolio strategy across regulatory intelligence, data, workflow, artifact generation, validation, and submission-related capabilities.
• Translate a long-range portfolio vision into a pragmatic, staged roadmap tied to measurable customer and business outcomes.
• Define and prioritize the highest-value customer problems to solve, especially where better regulatory change detection, impact assessment, workflow orchestration, and compliant execution can create meaningful differentiation.
• Drive product portfolio rationalization and consolidation, ensuring overlapping capabilities are simplified, modernized, or absorbed into a more coherent platform experience rather than expanded in parallel.
• Partner closely with Engineering, Architecture, Design, Data/AI, Services, Sales, Customer Success, and senior business leaders to align strategy, sequencing, tradeoffs, and execution.
• Establish clear portfolio investment priorities and product operating rhythms, including annual planning, roadmap governance, business cases, KPI tracking, and outcome reviews.
• Shape the Life Sciences AI strategy in partnership with technical leaders, with a focus on intelligent workflows, explainable decision support, governed automation, and future agentic capabilities that operate safely inside regulated processes.
• Work directly with customers and prospects to understand regulatory operations pain points, validate product-market fit, and ensure the roadmap is grounded in real-world workflows across labeling, submissions, compliance, and lifecycle change management.
• Build clarity where complexity exists: turn broad themes and fragmented backlogs into a focused strategy with explicit choices, sequencing, ownership, and expected impact.
• Lead, coach, and elevate product managers and cross-functional teams, while setting a high bar for strategic thinking, customer empathy, analytical rigor, and execution discipline.

Qualifications

• 10+ years of product management experience, with significant time leading complex B2B software portfolios, platforms, or multi-product businesses.
• Average of several years in a senior product leadership role with ownership for portfolio strategy, roadmap, investment decisions, and cross-functional execution.
• Strong experience in Life Sciences enterprise software or adjacent regulated domains, such as regulatory, labeling, submissions, quality, safety, clinical, medical device, or data/workflow platforms.
• Demonstrated success modernizing or consolidating fragmented products into more scalable platform-based offerings.
• Strong product judgment in workflow-heavy, data-rich, enterprise environments where trust, traceability, and operational reliability matter.
• Experience partnering deeply with engineering and architecture teams on platform strategy, API/integration strategy, data models, workflow systems, and AI-enabled capabilities.
• Ability to balance near-term business realities with long-term platform direction.
• Strong commercial instinct, including experience partnering with go-to-market teams, supporting enterprise deals, and building product cases tied to growth, retention, and margin.
• Exceptional communication and executive presence, with the ability to bring clarity to ambiguity and align senior stakeholders around choices.

Preferred Qualifications

• Experience with global regulatory or labeling workflows, health authority data, regional submissions, structured content, or artifact generation.
• Knowledge of regulated software environments and controls, including auditability, validation, and human-in-the-loop review.
• Experience introducing AI/ML or intelligent automation into enterprise workflows in a governed and explainable way.
• Experience in both software product environments and service-heavy operating models, with the ability to help move organizations toward more scalable SaaS and platform motions.

Why This Role Matters

Life Sciences is at an inflection point. Customers increasingly want fewer disconnected tools, better workflow integration, stronger traceability, and more proactive intelligence embedded directly into the work they do every day. LexisNexis is investing to meet that need by evolving from fragmented products toward a more unified Life Sciences platform that supports regulatory insight, workflow execution, audit readiness, and scalable AI-enabled operations. This role is central to making that transition real.

Pay and Benefits

U.S. National Base Pay Range: $136,100 - $252,800. Geographic differentials may apply in some locations to better reflect local market rates. If performed in New Jersey, the base pay range is $172,172 - $275,028. This job is eligible for an annual incentive bonus. We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. Click here to access benefits specific to your location.