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5 дней назад

Research Product Manager III (Bioinformatics)

105 000 - 145 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Research Product Manager III (Bioinformatics): Managing the software lifecycle for bioinformatics products supporting translational cancer research, diagnostic development, and clinical use with an accent on regulatory compliance, quality processes, and systems validation. Focus on prioritizing features, coordinating incident resolution, managing data contracts, and supporting software used with cancer genomics and next-generation sequencing data.

Location: Chicago, United States

Salary: $105,000–$145,000 per year

Company

hirify.global develops precision medicine and healthcare technology that connects real-world evidence and genomic data to support clinical decision-making.

What you will do

  • Manage software development lifecycle processes for bioinformatics software.
  • Coordinate with quality and regulatory teams and support quality processes.
  • Triage incidents, coordinate stakeholders, and manage issue resolution.
  • Collect, prioritize, and manage feature requests for software development.
  • Interface with downstream engineering product managers during implementation and manage data contracts.
  • Maintain comprehensive documentation and provide responsive support to software stakeholders.

Requirements

  • Bachelor’s or master’s degree in a scientific discipline.
  • Significant experience in medical device development and regulatory submissions.
  • 2–4 years of relevant experience in diagnostics product development.
  • Familiarity with US FDA and EU IVDR regulatory frameworks.
  • Experience with diagnostic products, clinical software regulatory requirements, algorithms development, and systems validation and verification.
  • Strong communication skills and the ability to work effectively in interdisciplinary teams.

Nice to have

  • Successful submissions to US and international regulatory agencies.
  • Experience in cancer genetics, immunology, or molecular biology.
  • Experience working with next-generation sequencing data.
  • Experience communicating insights and presenting concepts to diverse audiences.

Culture & Benefits

  • Benefits may include incentive compensation and restricted stock units.
  • Medical and other benefits may be available depending on the position.
  • Work supports interdisciplinary collaboration across product, engineering, quality, regulatory, and research functions.

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