Research Product Manager III

Tempus AI, Inc.; Chicago (IL); On-site; USD 105,000 - 145,000; Full time

Benefits offered by this job

Benefits package

Job summary

Tempus AI, Inc. is seeking a Sr. Technical Product Manager for Bioinformatics Software to lead regulation-driven product strategy and lifecycle for diagnostic software in oncology and related arenas.

You will collaborate with quality/regulatory teams, manage incidents, and prioritize feature requests while interfacing with engineering and product managers to ensure compliant, high-impact software solutions.

Qualifications

• Bachelor's or Master’s in a scientific discipline required.
• Significant experience in medical device development and regulatory submission.
• 2-4 years in diagnostics product development.
• Familiarity with US FDA and EU IVDR regulatory frameworks.
• Experience with diagnostic products, software regulatory requirements, and algorithms development.
• Top candidates will have significant experience in regulated device development.

Responsibilities

• Managing software development lifecycle processes.
• Engaging with the quality and regulatory team and supporting quality processes.
• Incident management: triage, coordinate, and resolve issues.
• Stakeholder support: provide dedicated and responsive support to users of the bioinformatics software.
• Feature request intake and prioritization: collect, prioritize, and manage feature requests.
• 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.

Skills

Regulatory knowledge

Diagnostics product development

Medical device development

FDA/EU IVDR familiarity

Education

Bachelor's or Master's in a scientific discipline

Job description

Sr. Technical Product Manager for Bioinformatics Software

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.

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.
• 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.

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.

Benefits

• 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.

Tempus was founded in August of 2015 by Eric Lefkofsky, after his wife was diagnosed with Breast Cancer. Shortly after he founded the company in an effort to bring the power of technology and artificial intelligence to cancer care, he convinced Ryan Fukushima to join as the company’s first employee. Ryan and Eric began assembling a world class team, focused on building the first version of a platform capable of ingesting real time healthcare data in an effort to personalize diagnostics. We built the platform for oncology and have expanded it to neuropsychiatry, cardiology, infectious disease (through COVID), and radiology. Despite our rapid growth, our mission remains the same—to help make sure patients are on the right drug at the right time, so they can live longer and healthier lives. We’re looking for people who can change the world. Who question the status quo and don’t shy away from tough problems. For the builders who are never done building and the learners who are never done learning. We’re looking for passionate people with undying curiosity. Those who want to attack one of the most challenging problems mankind has ever faced. Head on.