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Head of Project Management

Part-time

Integrated Resources Inc

Strong performance in this role enables the Diranersen PDC Lead to focus on enterprise strategy, external engagement, and key inflection-point decisions. What You ll Do Partner 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. Drive 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. Lead coordination across core functions including Clinical Development, Regulatory Affairs, Medical and Patient Engagement, Market Access and Commercial, and CClient/Supply to ensure clear accountability, alignment, and delivery aProductst key milestones. Provide oversight of device integration to ensure these critical workstreams are fully connected to the overall asset strategy and execution. Own 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. Track performance and drive on-time, high-quality execution while leading risk management through identification, mitigation, and escalation of key program risks. Lead 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. Maintain decision logs, action tracking, and governance discipline, and ensure transparent, fact-based escalation of key risks and decisions. Operate as a central connector across a complex, global matrix and influence senior stakeholders across R&D and Commercial without direct authority. Ensure the program reflects the urgent unmet need in Alzheimer s Disease and remains externally informed throughout development. Qualifications 10 years experience in drug development and commercialization with exceptional business acumen and executive, general management perspective. Demonstrated strong analytical and leadership skills, including creative, problem-solving mindset. Outstanding relationship building and communication skills, including ability to navigate throughout the organization and with individuals at all levels. Experience establishing and managing highly effective external collaborations, including familiarity with contractual, financial and compliance considerations. Very Strong project leadership (scoping project goals, stakeholder planning, etc.) and project management skills required. Prior experience working within a Product Development & Commercialization organization, Global Medicines Development, or cross-functional R&D/commercial team is preferred; Job Level: Management Why *? As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. At *, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. [a to learn more about our DE&I effortsAll 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. *** is an E-Verify Employer in the United States.

Vacancy posted 13 hours ago
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