Leads national account access strategy for OptumRx and Emisar, building payer relationships, negotiating contracts, and coordinating cross-functional teams to secure access for BridgeBio’s therapy portfolio.
Leads international pricing and reimbursement strategy to secure sustainable patient access, shaping value narratives, HTA submissions, payer engagement, and negotiations across markets for innovative therapies.
Leads pharmaceutical sciences and CMC strategy across clinical and commercial programs, guiding multidisciplinary teams through development, manufacturing, regulatory interactions, and lifecycle management.
Oversee clinical and commercial drug product manufacturing at contract manufacturers, support batch disposition and quality investigations, and drive process monitoring and continuous improvement across commercial operations.
Own the People and Legal technology and AI roadmap, architect enterprise platforms, lead vendor and implementation decisions, and scale governed AI solutions into production while ensuring reliable, compliant operations.
Leads commercial drug product manufacturing at contract manufacturers, overseeing routine production, technical transfers, validation, documentation, quality events, and cross-functional delivery for the Ecaleret program.
Own monthly close and general ledger accounting for complex accounts, preparing journal entries, reconciliations, analyses, and audit support while maintaining SOX-compliant controls and documentation.
Prepare and coordinate quarterly and annual SEC reporting, research complex accounting matters, maintain controls and policies, and improve reporting processes while partnering across accounting and business teams.
Leads statistical programming across clinical studies and regulatory submissions, combining hands-on programming with CRO oversight, cross-functional coordination, and development of compliant, efficient programming standards and tools.
Own day-to-day transfer pricing across entities and lead tax consolidation, effective tax rate, and cash-tax forecasting, building repeatable models and translating results into practical guidance for cross-functional teams.
Execute, analyze, and report biological assays for preclinical programs, including experiments measuring small-molecule inhibition of target proteolytic enzymes and maintaining compliant laboratory operations.
Lead end-to-end intellectual property strategy for pharmaceutical assets, including global patent prosecution, freedom-to-operate assessments, lifecycle exclusivity, and practical counsel to cross-functional teams.
Leads U.S. HCP marketing for BBP-418, shaping brand strategy and launch campaigns, coordinating cross-functional teams, and measuring promotional effectiveness to support brand growth and patient identification.
Leads clinical strategy and scientific programs to improve patient outcomes, translating clinical opportunities and evidence into studies, scientific content, and collaborations that support clinical adoption.
Manages analytical development, quality control, and stability programs at contract manufacturing sites, supporting clinical asset development and regulatory filings through method validation, batch release, and quality investigations.
Leads clinical pharmacology and pharmacometrics strategy across drug development, overseeing quantitative modeling, study design, CROs, and regulatory submissions to guide decisions and support patient-focused programs.
Serve as a field-based scientific expert for Medical Affairs, building healthcare relationships, sharing balanced scientific information, shaping territory medical plans, and translating clinical insights into strategy.
Own sales operations for the field organization, including incentive compensation, CRM and reporting, field analytics, and operational processes, while advising commercial leadership with performance insights.
Develops sourcing strategies and manages commercial contracts with Contract Manufacturing Organizations, partnering across supply chain, legal, finance, CMC, and quality to strengthen supplier performance and contractual compliance.
Oversee general ledger close and technical accounting, own SEC filing sections and internal controls, and lead a team while improving accounting processes and partnering across the business.
The Commercialization Project Manager will report directly to the Head of International Supply Chain and will work remotely from the Netherlands.
Leads international health economics and outcomes research strategy, overseeing evidence generation and HTA submissions to support pricing, reimbursement, and timely patient access across markets.
Develops board- and executive-ready commercial narratives, bringing together launch, market access, pricing, and marketing work while coaching leaders to create clear, consistent presentations.
Lead quality oversight for drug product contract manufacturers, reviewing batch records and release activities while ensuring cGMP compliance and resolving quality events across manufacturing operations.
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