Global Development IT is seeking a strategic, hands-on Senior Manager to serve as Product Lead for Regeneron's enterprise generative-AI document-authoring platform. You will be responsible for a multi-phase implementation that delivers governed, scalable AI capabilities across Clinical, Regulatory, Medical Affairs, Labeling, and other Global Development domains. Partnering with business and technology stakeholders, you will align platform strategy to scientific, regulatory, and operational needs, ensuring secure, compliant, and high-impact outcomes.
Reporting to the Head of Enabling Technologies, you will drive the full product lifecycle-from vision and roadmap through design, build, validation, launch, and optimization. Your blend of clinical-process know-how, agile product leadership, and deep AI expertise will accelerate content creation, improve quality, and reduce cycle times for regulated documents.
In this role, a typical day might include the following:
- Leading stand-ups, refining backlogs, and approving user stories for AI-powered authoring features
- Facilitating workshops with Clinical, Regulatory, and Medical Affairs teams to gather requirements and prioritize enhancements
- Reviewing solution architecture to enforce security, privacy, and GxP compliance across RAG, MCP, LLM, Copilot, and Claude integrations
- Tracking sprint progress, surfacing risks, and updating program leadership on scope, budget, and ROI
- Defining guardrails for citizen development and coordinating change-control / governance forums
- Monitoring platform adoption and performance to identify automation and continuous-improvement opportunities
This job might be for you if you:
- Translate sophisticated Global Development document workflows into intuitive, AI-enabled products
- Excel at influencing cross-functional teams without direct authority and communicating clearly with executive stakeholders
- Thrive in agile environments, balancing tactical delivery with long-term platform strategy
- Enjoy partnering with data-science teams to embed generative AI into regulated processes
- Keep current on industry standard processes and proactively incorporate them into product roadmaps
- Maintain a "get-it-done" attitude and balance multiple high-priority initiatives simultaneously
In order to be considered for this role, you must have:
- BS/BA with 8-10 years validated experience (or MS/MBA with 6+ years as an equivalent), including 3 years in enterprise SaaS and 1+ year delivering generative/agentic-AI solutions
- Proven success leading end-to-end GxP implementations of AI document-authoring platforms, using agile/DevOps methods
- Validated expertise in RAG, MCP, LLMs, Copilot, Claude, and integration across Clinical, Regulatory, and Medical Affairs systems
Salary Range (annually)
$134,400.00 - $219,200.00
