обновлено 14 дней назад
Director Program Management (Genomics)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Director Program Management (Genomics): Leading complex cross-functional programs across product development, clinical operations, laboratory improvements, digital platforms, and regulatory compliance with an accent on PMO governance, executive communication, and delivery accountability. Focus on building program management capabilities, managing healthcare-regulated initiatives, mitigating risks, and aligning resources across matrixed teams.
Location: Remote, United States; periodic travel may be required.
Company
operates in genomics, clinical diagnostics, laboratory testing, and healthcare technology.
What you will do
- Lead strategic, cross-functional programs across product development, revenue cycle management, laboratory improvements, and digital platforms.
- Develop PMO capabilities, governance practices, tools, KPIs, timelines, budgets, and reporting structures.
- Partner with Product, Clinical, Lab Operations, Informatics, Software Engineering, Regulatory, and Quality leaders to define priorities and success metrics.
- Facilitate steering committee and stakeholder meetings, communicate progress to executive leadership, and provide risk assessments and decision requests.
- Manage dependencies, resource allocation, risks, and issue escalation across the program portfolio.
- Mentor project teams and conduct post-implementation reviews to improve future initiatives.
Requirements
- Must be based in the United States and work remotely.
- Bachelor’s degree in Life Sciences, Health Administration, Business, Engineering, or a related field.
- 10+ years of experience in new product development, program management, or portfolio management within biotech, life sciences, or diagnostics.
- 8+ years of program or portfolio management experience and 3+ years in people leadership.
- Experience managing large-scale cross-functional programs involving complex systems integration and business process transformation.
- Strong understanding of laboratory workflows, clinical testing, healthcare regulations, and tools such as Microsoft Project, Smartsheet, or PKIT.
Nice to have
- Experience in regulated laboratory environments, diagnostics, genomics, or molecular testing.
- PMP, PgMP, SAFe Agilist, or equivalent certification.
- Experience supporting the development or commercialization of clinical laboratory tests.
Culture & Benefits
- Primarily remote, office-based work with collaboration across product, clinical, laboratory, operational, and technical teams.
- Work within regulated healthcare, laboratory, quality, and compliance environments.
- Inclusive workplace and equal opportunity employment practices.
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