
1001 - 5000 employees
Founded 2015
🧬 Biotechnology
🤖 Artificial Intelligence
Healthcare • Biotechnology • Artificial Intelligence
Tempus AI is an advanced healthcare technology company that specializes in precision medicine through the use of AI and genomic profiling. The company provides innovative solutions across various medical fields, including oncology, cardiology, neurology, and psychiatry. Tempus enables healthcare providers to make informed treatment decisions by integrating real-world data, clinical trial matching, and algorithmic testing to improve patient outcomes and accelerate drug development.
🕒 May 6
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1001 - 5000 employees
Founded 2015
🧬 Biotechnology
🤖 Artificial Intelligence
Healthcare • Biotechnology • Artificial Intelligence
Tempus AI is an advanced healthcare technology company that specializes in precision medicine through the use of AI and genomic profiling. The company provides innovative solutions across various medical fields, including oncology, cardiology, neurology, and psychiatry. Tempus enables healthcare providers to make informed treatment decisions by integrating real-world data, clinical trial matching, and algorithmic testing to improve patient outcomes and accelerate drug development.
• 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.
• 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.
• incentive compensation • restricted stock units • medical and other benefits depending on the position
Apply Now🕒 April 28
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