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8 дней назад

Program Manager, Product Development (Biotechnology)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Program Manager, Product Development (Biotechnology): Leading the development and launch of new assays and initiatives within a product development organization with an accent on project planning, cross-functional coordination, and regulatory requirements. Focus on managing scope, risks, resources, timelines, deliverables, and change impacts across clinical laboratory and biotechnology projects.

Location: Chicago, United States

Company

Develops an AI-enabled precision medicine platform that connects real-world evidence and genomic data to support clinical care and cancer treatment decisions.

What you will do

  • Lead the development and launch of new assays and initiatives within the Product Development organization.
  • Develop and maintain detailed project plans throughout the project lifecycle using approved project management tools.
  • Coordinate with the Sponsor, Core Team Lead, and cross-functional Core Team to define scope, requirements, resources, risks, timelines, and deliverables.
  • Prepare agendas, facilitate structured project meetings, and communicate project updates through status reports and dashboards.
  • Identify tradeoffs between budget, resources, and schedule; escalate decisions and analyze the impact of change requests.
  • Confirm completion of project outputs and documentation, and incorporate lessons learned into future planning and execution.

Requirements

  • Four-year college degree, preferably in a scientific, clinical, technical, or business discipline.
  • At least 3 years of project management experience and understanding of formal project management methodologies.
  • Experience in the biotechnology, clinical laboratory, or medical device industry.
  • Proficiency with project management software such as Smartsheet, MS Project, Coda, or JIRA.
  • Familiarity with CLIA, CAP, GMP, NYSDOH, and FDA regulations and requirements.
  • Exceptional leadership, verbal and written communication, and interpersonal skills, with the ability to communicate across functions and organizational levels.
  • High attention to detail and the ability to complete projects on time with accuracy and attention to quality.
  • Ability to build and maintain effective relationships and trust within a diverse, results-driven organization.
  • Ability to work independently with minimal supervision in a fast-paced environment, learn new skills quickly, and adapt to new processes and changes.

Nice to have

  • Project management certification, preferably PMP.

Culture & Benefits

  • Work in precision medicine, cancer genomics, and clinical healthcare technology.
  • Benefits may include incentive compensation, restricted stock units, medical benefits, and other benefits depending on the position.
  • Equal opportunity employment environment.

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