GE HealthCare

Chief Marketing Officer

• Lead the U.S. field marketing strategy and execution across Oncology for the pharmaceutical diagnostics (PDx) segment.
• Drive regional demand generation and deliver on-label product related education.
• Coordinate go-to-market execution with sales and tailor national marketing strategies to local market dynamics.
• Manage and mentor a team of Regional Field Marketing Managers.
• Plan and lead execution of regional/local demand generation initiatives including campaigns and educational programming.
• Partner with sales leadership to develop compliant territory specific go-to-market plans and customer activation activities.
• Design and track KPIs for regional marketing execution including lead generation and campaign response metrics.
• Collaborate with Marketing Franchise team to develop tailored marketing messaging and field kits based on customer insights.
• Work with Regulatory, Legal and Compliance stakeholders for appropriate design and execution of field marketing activities.
• Coordinate presence at key regional and local events in collaboration with events and franchise teams.

Director, Field Marketing – Oncology Referrers

Compliance

• Develop, oversee and drive global regulatory strategies for assigned development programs and marketed products in US, and other priority markets supported by the regional regulatory teams.
• Serve as the senior regulatory lead in interactions with major health agencies including FDA, leading high-stakes negotiations and ensuring high-quality briefing packages and responses.
• Partner with R&D, CMC, Manufacturing, Clinical, Medical, Quality, Commercial, and Supply Chain teams to integrate regulatory requirements into global product strategies, development plans, and launch readiness.
• Lead, mentor, and develop a global team of regulatory professionals across multiple regions.
• Ensure global compliance across development, submissions, registration maintenance, and post-market activities.
• Support due diligence activities for partnerships, acquisitions, and in-licensing opportunities by assessing regulatory risks, pathways, and development strategies.

Senior Director, Regulatory Affairs, Radiopharma

• Define and drive the global lifecycle regulatory strategy aligned with corporate, portfolio, and product objectives
• Act as a strategic partner to senior leadership, communicating risks, opportunities, and regulatory scenarios
• Lead, coach, and develop a high-performing global regulatory team
• Oversee all post-approval regulatory activities, including variations, renewals, and regulatory commitments
• Lead regulatory strategy for post-approval changes, including impact assessment, pathway optimization, and risk mitigation
• Ensure compliance with global regulatory requirements and evolving health authority expectations
• Partner with RA-CMC to align regulatory strategies for technical and manufacturing changes
• Ensure timely, high-quality execution of lifecycle submissions through effective planning, tracking, and team accountability

Director, Regulatory Affairs – Market Products, Radiopharma

Product Specialist

• Cultivate and maintain strong relationships with healthcare stakeholders within the hospital
• Deliver on quarterly & annual orders and revenue sales targets
• Leverage product knowledge in our Patient Monitoring and Patient Care portfolio to drive funnel growth for the region
• Demonstrate expertise in customers’ installed base and develop sales proposals
• Collaborate with the account community team to support co-developed negotiation strategies
• Reduce cycle time by leveraging Salesforce.com to track customer and account activity

Director, Field Marketing – Oncology Referrers

Senior Director, Regulatory Affairs, Radiopharma

Director, Regulatory Affairs – Market Products, Radiopharma

Product Sales Specialist, Patient Monitoring