Brittney Belden

Senior Director, Program Management - Therapy Portfolio Lead @Edwards Lifesciences

Costa Mesa, CA, US
EMAILS
b••••••••@edwards.com
MOBILE NUMBERS
+19•••••••79

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WORK HISTORY

Aug 2024 — Present

Senior Director, Program Management - Therapy Portfolio Lead @Edwards Lifesciences

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Lead enterprise-level portfolio strategy and execution for a global transcatheter therapy platform spanning innovation, clinical evidence, and commercialization. Established and scaled a Program Management Office with end-to-end accountability for governance, investment prioritization, and delivery across a multi-program portfolio.Partner closely with executive leadership to define strategic imperatives, operating models, and portfolio trade-offs that directly inform annual operating plans, funding decisions, and launch commitments. Drive business-wide change to enable a platform-based operating model, improve transparency, and accelerate decision-making across highly matrixed global teams.Build and develop high-performing program management leaders capable of delivering in highly complex environments while maintaining focus on patient impact, regulatory rigor, and commercial readiness.

EDUCATION

2007 — 2007

University of Oxford

Political Science, Philosophy

2005 — 2009

University of San Diego

Bachelor of Arts, Political Science and Philosophy

ABOUT BRITTNEY BELDEN

Enterprise portfolio leader with deep expertise in advancing first-of-their-kind medical technologies from innovation through global launch. Proven partner to executive leadership in shaping strategy, defining operating models, and driving disciplined execution across highly complex, regulated environments.Known for building and scaling PMO organizations, accelerating executive decision-making, and translating ambiguity into actionable plans that deliver regulatory approvals, market entry, and commercial impact. Build and develop high-performing program management leaders capable of delivering in ambiguous, high-risk environments while maintaining focus on patient impact, regulatory rigor, and commercial readiness.

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