Associate Director Product Management

Regeneron

Confirmed live today High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Warren, NJArmonk
Employment
Full-time
Posted
36 days ago
Freshness
Confirmed live today

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Similar $210k
$159k $256k
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This listing doesn't post a salary. Most similar roles pay $173,518–$246,975.

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About Regeneron

Regeneron is a leading science-driven biotechnology company that invents, develops, and commercializes life-transforming medicines for serious diseases.

Regeneron currently has 73 open roles on FindRole.

Listed pay typically runs $134,400–$241,200 across 46 roles with salary data.

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At a glance

TL;DR · Associate Director Product Management

The Assoc Dir Product Management serves as a leader within the Global Development IT Delivery & Operations organization, overseeing a portfolio of technology products. This role involves leading, coaching, and developing a team of Product Leads and Product Analysts to manage strategy, delivery, and continuous improvement. Key responsibilities include owning the multi-product domain strategy for standards-led protocol digitization, Digital Data Flow, and human sample lifecycle management. The successful candidate will build domain capabilities, manage senior stakeholder relationships, and oversee end-to-end implementation, governance, and compliance. Required skills include command of ICH M11/USDM, CDISC SDTM/ADaM, and experience with AI multi-agent orchestration, REST/GraphQL APIs, and ETL/ELT pipelines. The role solves complex problems regarding biospecimen standards, traceable data lineage, and regulated-AI governance within pharmaceutical global development.

What you'll do

  • Lead, coach, and develop a team of Product Leads and Product Analysts across multiple technology domains.
  • Own the multi-product domain strategy, vision, and roadmap for protocol digitization, data flow, and sample lifecycle management.
  • Manage senior stakeholder relationships across business partners, corporate IT, and external vendors to align technology with enterprise priorities.
  • Chair domain steering committees and governance forums to ensure consistency and reuse across all product lines.
  • Oversee end-to-end product ownership including requirements, testing, risk-based CSV, and ITIL-aligned release and incident processes.
  • Set direction for regulated-AI governance and multi-agent orchestration aligned to 21 CFR Part 11 and GxP standards.
  • Drive build-vs-buy assessments, RFPs, software contracting, and vendor performance management for the product portfolio.
  • Direct the establishment of digital protocols and structured schedules of activities as the system of record for clinical data.

What we're looking for

  • Strong command of ICH M11/USDM, CDISC SDTM/ADaM, controlled terminology, and standards governance.
  • Demonstrated delivery of structured protocol authoring and protocol-to-data automations with traceable lineage into SDTM/ADaM.
  • Experience with USDM-aligned tools (e.g., Nurocor) or equivalent MDRs.
  • Practical understanding of human sample workflows, central/specialty lab operating models, and biospecimen/lab and SAP/EDC integrations.
  • Experience managing technology capability identification, selection, implementation, and operations, including LIMS/LIS integrations with EDC, IRT, CTMS, and analytics.
  • Experience applying AI and multi-agent/agentic systems with human-in-the-loop controls, plus technical fluency in REST/GraphQL APIs and ETL/ELT data pipelines.
  • Knowledge of pharmaceutical Global Development business capabilities, SDLC, and ITSM/ITIL frameworks with strong project and budget management skills.
  • Familiarity with SQL/Python or R for prototyping/validation and MLOps in regulated environments (preferred).

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