Job description

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. Sr. Technical Product Manager for Bioinformatics Software Passionate about making a difference in the world of cancer genomics? With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don t have the infrastructure or expertise to make sense of this data. We’re on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. 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 significant experience in regulated device development. This role will report to the head of Bioinformatics and support software product development functions. 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 isues. 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 Pay Range: $105,000-$145,000 The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position. We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Requirements

Must-haves

Passionate about precision medicine and advancing the healthcare industry?
Sr. Technical Product Manager for Bioinformatics Software
Passionate about making a difference in the world of cancer genomics?
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 isues.
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.
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
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Nice-to-haves

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Keywords to mirror

Platform: workday
Effort: long