Ph3About This Role /h3pThis person is a hands‑on leader with responsibility for advancing the execution of significant elements of program strategy and cross‑functional execution for the Dravet (Zorevunersen) program. Strong performance in this role enables the Zorevunersen PDC Lead to focus on enterprise strategy, external engagement, and key inflection‑point decisions. /ppThis role requires a talented individual with experience integrating cross‑functional perspectives into program priorities, decisions, and execution. The individual will work closely with a diverse set of cross‑functional partners across the company and provide leadership within the cross‑functional PDC team as we prepare for potential global launch of Zorevunersen. /ph3What You’ll Do /h3pPartner with the PDC Lead to translate asset strategy into an actionable, integrated program plan and ensure alignment across clinical, regulatory, medical, access, and commercial functions. /ppDrive scenario planning and trade‑off analyses to support key strategic decisions, and integrate the external landscape, including competition, regulatory evolution, and advocacy insights, into program planning. /ppLead coordination across core functions including Clinical Development, Regulatory Affairs, Medical and Patient Engagement, Market Access and Commercial, and CMC/Supply to ensure clear accountability, alignment, and delivery against key milestones. /ppLead the preparation of the DASP (Disease Area Strategy Plan) as well as the communications team, including key external milestones, PR and earnings preparation, and internal communications. /ppProvide oversight of device integration to ensure these critical workstreams are fully connected to the overall asset strategy and execution. /ppProactively identify and resolve cross‑functional gaps or misalignments to maintain program momentum. /ppOwn the integrated development and operating plan, including timelines, critical path, milestones, deliverables, and resource and budget assumptions, ensuring all cross‑functional workstreams are fully integrated into the overall asset plan. /ppTrack performance and drive on‑time, high‑quality execution while leading risk management through identification, mitigation, and escalation of key program risks. /ppLead program governance in close partnership with the PDC Lead, including preparation and orchestration of PDC and sub‑team forums, structuring decision frameworks, and ensuring clarity on decision versus information topics. /ppMaintain decision logs, action tracking, and governance discipline, and ensure transparent, fact‑based escalation of key risks and decisions. /ppOperate as a central connector across a complex, global matrix and influence senior stakeholders across RD and Commercial without direct authority. /ppFoster a high‑performing, accountable, and collaborative team environment, and promote clarity of roles, decision rights, and ways of working. /ppEmbed patient‑centric thinking into program planning and execution by integrating insights from patient advocacy groups, key opinion leaders, and clinical experts. /ppEnsure the program reflects the urgent unmet need in Dravet syndrome and remains externally informed throughout development. /ph3Qualifications /h3p5+ years’ experience in drug development and commercialization with exceptional business acumen and executive, general management perspective. /ppDemonstrated strong analytical and leadership skills, including a creative, problem‑solving mindset. /ppAbility to rapidly identify key priorities, align strategic and tactical plans, and influence motivate cross‑functional teams. /ppOutstanding relationship building and communication skills, including ability to navigate throughout the organization and with individuals at all levels. /ppExperience establishing and managing highly effective external collaborations, including familiarity with contractual, financial and compliance considerations. /ppVery strong project leadership (scoping project goals, stakeholder planning, etc.) and project management skills required. /ppPrior experience working within a Product Development Commercialization organization, Global Medicines Development, or cross‑functional RD/Commercial team is preferred; rare disease and launch preparation experience are a plus. /ph3Job Level /h3pManagement /ppAll qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. /ppBiogen is an E‑Verify Employer in the United States. /p /p #J-18808-Ljbffr