Research Product Manager III
Tempus AI
Summary
We are looking for a highly motivated and capable technical product manager with extensive experience and interest in translational cancer research, diagnostic test development, and systems validation and verification. This position requires experience with diagnostic products, clinical regulatory requirements for software systems, and algorithms development. Top candidates will also have significant experience in regulated device development. This role will report to the head of Bioinformatics and support software product development functions.
Job description
Responsibilities
- Managing software development lifecycle processes.
- Engaging with the quality and regulatory team and supporting quality processes.
- Incident management: Promptly triage, coordinate, and manage the resolution of issues.
- Stakeholder support: Provide dedicated and responsive support to all stakeholders using the bioinformatics software.
- Feature request intake and prioritization: Collect, prioritize, and manage feature requests to guide software development.
- Interfacing with Product Managers of downstream engineering teams during implementation.
- Data contract management with downstream engineering teams.
- Documentation: Maintain comprehensive and up-to-date documentation for all bioinformatics software.
Required Experience
- Bachelors or M.S. in a scientific discipline
- Significant experience in medical device development and regulatory submission
- 2-4 years relevant experience in diagnostics product development
- Familiarity with US FDA and EU IVDR regulatory frameworks.
Ideal candidates will possess
- A track record of successful submissions to US and international regulatory agencies
- Experience in cancer genetics, immunology, or molecular biology
- Experience working with next-generation sequencing data
- Self-driven and works well in interdisciplinary teams
- Experience with communicating insights and presenting concepts to a diverse audience
Requirements
- Bachelors or M.S. in a scientific discipline
- Significant experience in medical device development and regulatory submission
- 2-4 years relevant experience in diagnostics product development
- Familiarity with US FDA and EU IVDR regulatory frameworks
- A track record of successful submissions to US and international regulatory agencies
- Experience in cancer genetics, immunology, or molecular biology
- Experience working with next-generation sequencing data
- Self-driven and works well in interdisciplinary teams
- Experience with communicating insights and presenting concepts to a diverse audience
Benefits
- Incentive compensation
- Restricted stock units
- Medical benefits
Company overview
Tempus AI, Inc. (NASDAQ: TEM) is a pioneering healthcare technology company founded in 2015 by Eric Lefkofsky in Chicago, Illinois. The company was established after Lefkofsky's wife was diagnosed with breast cancer, driving his mission to revolutionize cancer care through technology and artificial intelligence. Tempus specializes in applying AI to advance precision medicine by collecting and analyzing vast amounts of molecular, clinical, and genomic data. The company operates across multiple therapeutic areas including oncology, cardiology, radiology, neurology, psychiatry, and dermatology. Tempus provides comprehensive diagnostic services including next-generation sequencing (NGS), PCR profiling, and molecular pathology testing. Its AI-powered platform enables physicians to make real-time, data-driven decisions for personalized patient care and targeted therapies. The company went public in June 2024 and has expanded globally with operations in multiple countries. Tempus continues to innovate at the intersection of healthcare and artificial intelligence, aiming to ensure patients receive the right treatments at the right time for improved health outcomes.