Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Высокая руководящая роль в крупной биофармацевтической компании с четкой стратегической ответственностью и влиянием на программы R&D и решения по портфелю.
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Широкая зона влиянияКрупная биофармаВысокие требования к опыту
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Global Head, R&D Program Management & Therapeutic Area Portfolio Operations (Biopharma): Leading global R&D program management, development planning, and therapeutic area portfolio operations across complex drug development and regulatory programs with an accent on strategic planning, portfolio governance, and cross-functional delivery. Focus on building high-performing global project management teams, resolving organizational bottlenecks, and aligning timelines, costs, resources, and decisions across therapeutic areas.
Location: Hybrid, onsite three days per week, based in King of Prussia, Pennsylvania, USA, or Maidenhead, UK.
Company
hirify.global is a global biopharmaceutical leader developing innovative therapies for rare and serious diseases across immunology, hematology, cardiovascular and metabolic, respiratory, and transplant areas.
What you will do
Lead global development and regulatory project managers across complex R&D programs, New Product Development, and Life Cycle Management.
Drive strategic and operational planning across the R&D portfolio, balancing innovation, quality, timelines, costs, and resources.
Lead Therapeutic Area Portfolio & Operations, coordinating strategy, portfolio reviews, investment planning, due diligence, and cross-functional decision-making.
Identify delivery risks, organizational bottlenecks, and structural challenges, driving issues through resolution and supporting critical milestones.
Lead and develop a global project management organization across multiple functions and geographies, coaching leaders and strengthening execution.
Requirements
Bachelor's degree in a relevant scientific, business, or related discipline required; a Master's degree, MBA, or equivalent is preferred.
12+ years of progressive experience in project management, program management, and/or portfolio management within R&D, biotechnology, or pharmaceutical industries.
Experience leading complex, cross-functional R&D programs and global portfolios across multiple functions and geographies.
Experience managing large-scale development programs, portfolio initiatives, and organizational priorities in a complex matrix environment.
Strong understanding of pharmaceutical and biotechnology R&D processes, including drug development, clinical development, regulatory affairs, and Life Cycle Management.
Expertise in strategic and operational planning, portfolio management, risk assessment, resource planning, and project execution.
Experience with project and portfolio management methodologies, tools, and systems such as Microsoft Project, Planview, Smartsheet, or Jira.
Exceptional communication, influencing, change leadership, and executive reporting skills, including translating complex data into actionable recommendations for senior leadership.
Ability to influence senior leaders, navigate organizational complexity, resolve issues, drive decisions, and lead, coach, and develop high-performing global teams.
Strong strategic thinking, business acumen, operational judgment, and ability to operate at both strategic and tactical levels.
Nice to have
Advanced degree such as a Master's, MBA, or equivalent.
Culture & Benefits
Hybrid work arrangement with onsite attendance three days per week.
Leadership role within the Portfolio & Operations Excellence organization with global, cross-functional responsibilities.
Focus on accountability, collaboration, empowerment, connectivity, delivery, transformation, and continuous improvement.
Benefits information is provided through CSL's candidate benefits portal.
CSL supports inclusion and belonging and is an equal opportunity employer.
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