Head of Regulatory, Medical & CDU Technology Solutions

Regeneron Pharmaceuticals, Inc (USA); Kentucky; On-site; USD 255,000 - 425,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks an Executive Director to lead Reg, Medical & CDU Business Solution Delivery. You will own the platform strategy, drive multi-year roadmaps, and align capabilities with enterprise priorities across Regulatory Affairs, Medical Affairs and Clinical Data.

You will manage Directors, oversee budgets and vendor relationships, and ensure compliant operations across platforms such as Veeva RIM, Mediverse, iEnvision, and related clinical data tools.

Qualifications

• Bachelor’s degree in Computer Science, Information Systems, Business Administration, or a related field (Master’s degree preferred).
• 15+ years of progressive industry/relevant professional experience in enterprise-scale regulatory, medical affairs, or clinical data technology platforms.
• Proven experience managing budget and vendor contracts for a major function.

Responsibilities

• Own platform strategy and delivery for Reg, Medical & CDU technology portfolio.
• Lead a team of Directors across the domain and manage governance and budgets.
• Ensure regulatory compliance, data integrity, and audit readiness for submissions.
• Partner with Regulatory Affairs, Medical Affairs, and Clinical Development leadership to align roadmaps with business objectives.
• Represent Reg, Medical & CDU priorities in enterprise architecture and governance forums.

Skills

Budget management

Vendor management

Executive communication

Stakeholder management

Team leadership

Strategic planning

Regulatory information management

Education

Bachelor's degree in Computer Science or related field

Master’s degree preferred

Tools

Veeva RIM

Veeva Vault

Medical inquiry platforms

Clinical data platforms

Job description

Regeneron Pharmaceuticals, Inc. seeks an Executive Director to lead Reg, Medical & CDU Business Solution Delivery. You will own the platform strategy, drive multi-year roadmaps, and align capabilities with enterprise priorities across Regulatory Affairs, Medical Affairs and Clinical Data.

You will manage Directors, oversee budgets and vendor relationships, and ensure compliant operations across platforms such as Veeva RIM, Mediverse, iEnvision, and related clinical data tools.