
1001 - 5000 employees
Founded 2015
🏥 Healthcare
🧬 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.
🔥 12 hours ago
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1001 - 5000 employees
Founded 2015
🏥 Healthcare
🧬 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.
• Maintain and expand collaborations with pharmaceutical partners and CROs to support rapid study start-up • Oversee deliverables for a subset of pharmaceutical clients, focusing on quality and expeditious timelines • Manage day-to-day execution of studies within the TIME network from study start-up through closure • Ensure customer satisfaction and continued growth of Tempus business • Apply knowledge of clinical trial development and study start-up to prepare a portfolio of trials for the network of sites • Help create innovative tactics, processes, tools, systems and strategies to accelerate cancer clinical trials • Collaborate with site operations, medical affairs, pathology, bioinformatics and data science teams • Identify risks to assigned studies and work with internal and external partners to resolve issues
• Occasional travel required, varying by project • Bachelor's Degree and 4+ years of experience working with complex clinical trials from a site, sponsor or CRO perspective • Highest level knowledge of FDA regulations, GCP, study start-up, clinical trial agreements, trial budgets, IRB submission and pharma operations • Collaborative team player • Exceptional customer service skills and strong interpersonal and problem-solving skills • Proven track record of setting and achieving high personal standards of performance • Highly organized and systematic, with superb attention to detail and ability to complete tasks accurately with an eye toward process improvement • Flexible and adaptable; ability to work independently in a fast-paced environment • Experience with rapid site activation preferred • Experience with research networks preferred • Clinical research project management experience preferred
• Incentive compensation may be offered • Restricted stock units may be offered • Medical and other benefits depending on the position
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