project managementrisk managementprogram managementmicrosoft projectpharmaceuticalsoncologybiotechdrug developmentclinical development
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$179к-239к/год
$190к$230кмедиана$250к
По похожим ролям (50) ~ $230к/год
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У роли четкий директорский уровень и понятная зона ответственности в разработке онкологических препаратов, с прямой связью работы с результатами для пациентов.
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Высокая ответственностьОнкологияПонятные требованияАкции и льготы
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Director, Oncology Program Management (Biotech/Pharmaceuticals): Leading oncology drug development and product lifecycle programs with an accent on global development strategy, cross-functional alignment, and integrated project planning. Focus on managing milestones, dependencies, risks, budgets, governance, and strategic decision-making across clinical and drug development teams.
Location: Remote (US); travel as needed.
Salary: $178,700–$238,700 annually.
Company
hirify.global develops medicines with a focus on fighting cancer and expanding patient access to affordable treatments.
What you will do
Lead program management for oncology drug development and product lifecycle management.
Partner with team leadership to develop global product development strategies and establish program team communication processes.
Plan and execute projects, maintaining integrated project plans, milestones, dependencies, critical paths, deliverables, and project visuals.
Facilitate cross-functional planning, team charters, scope definition, stakeholder alignment, governance updates, meetings, minutes, action tracking, and progress reporting.
Implement project and risk management practices and oversee project budget planning and control.
Provide additional leadership as appropriate, including alliance management for drug development partners and oversight steering committees.
Requirements
Bachelor’s degree plus 10+ years of experience in clinical and drug development within the biotech or pharmaceutical industry, or a master’s degree or higher plus 7+ years of relevant experience.
Experience leading oncology drug development or product lifecycle management programs.
Experience with cross-functional stakeholder alignment, integrated project planning, milestone and dependency management, risk management, and budget oversight.
Efficient use of Microsoft Word, Excel, Project, and Outlook.
Ability to work remotely from the United States and travel as needed.
Nice to have
PMP certification.
Culture & Benefits
Values include Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit.
Benefits include medical, dental, and vision coverage; 401(k); FSA/HSA; life insurance; paid time off; and wellness programs.
Eligible employees may participate in annual bonus or incentive compensation plans, discretionary equity awards, and the Employee Stock Purchase Plan.
Equal opportunity employment and reasonable accommodation are provided in accordance with applicable law.
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