Associate Director, Clinical On-market R&d Program Manager

Illumina

Base: $170,600 - $255,800; bonus/equity: variable ...
Hybrid
Molecular assay development knowledge
Ivd/dx regulatory requirements understanding
Matrixed environment leadership experience
Illumina is seeking an Associate Director, Clinical On-Market R&D Program Manager to oversee the sustainment of its clinical product portfolio, particularly in genomic technologies. The role emphasizes collaboration across departments and requires a strong background in molecular biology, project management, and leadership skills

Job Summary

  • This role serves as the Clinical Technical Lead and R&D Portfolio Manager for on-market product sustainment within Illumina's diverse Clinical Portfolio.
  • The ideal candidate must be a skilled team leader with strong negotiating and influencing skills capable of working in a matrixed environment.
  • Employees are eligible for variable cash programs, equity, and a comprehensive benefits package including health/dental/vision and retirement benefits.

Matching Summary

Match Score: 85

Illumina is seeking an Associate Director, Clinical On-Market R&D Program Manager to oversee the sustainment of its clinical product portfolio, particularly in genomic technologies. The role emphasizes collaboration across departments and requires a strong background in molecular biology, project management, and leadership skills.

Salary

Base: $170,600 - $255,800; Bonus/Equity: Variable cash program and equity eligible; Benefits: Health/dental/vision, retirement, paid time off

Skills & Requirements

Must-have

  • Molecular assay development knowledge
  • IVD/Dx regulatory requirements understanding
  • Matrixed environment leadership experience
  • Project budget and timeline creation
  • Cross-functional collaboration skills

Nice-to-have

  • PMP certification preferred
  • Strong negotiating and influencing skills
  • Experience with NGS assays
  • Portfolio management proficiency
  • Ability to work independently

Key Requirements

  • 15+ years relevant experience managing product development
  • M.S./Ph.D. in Genomics, Genetics, or related field
  • Proficiency with MS Project for scheduling
  • Current PMP certification desired
  • No visa sponsorship available

Work Rights

Not specified

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