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Tempus

👥 1001-5000💰 $100,000,000 Debt Financing about 2 years agoArtificial Intelligence (AI)BiotechnologyMedicalMachine LearningPrecision MedicineHealth Care📈 Public Company
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Tempus is a company specializing in innovative data management solutions, focusing on leveraging advanced technologies to enhance data-driven decision-making.

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Jobs at this company:

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🔥 Scientific Affairs Liaison
Posted 12 days ago

📍 U.S.

🔍 Healthcare and biotechnology

  • Advanced scientific or medical degree (e.g., PhD, PharmD, MD, BSN, MSN, NP, GC).
  • Preferred: PhD, PharmD, GC.
  • Fundamental understanding of molecular testing and oncology, including NCCN and ESMO guidelines.
  • Exceptional interpersonal communication and writing skills.
  • Public speaking skills and ability to communicate scientific topics to diverse audiences.
  • Knowledge of genomic laboratory-developed testing, and familiarity with CLIA-88', CAP, Sunshine Act, and FDA regulations.
  • Strong navigation skills in a fast-moving company environment.
  • Ability to travel (<20%).
  • Self-starter with an ownership mindset able to deliver on tight timelines.

  • Function as an internal scientific/technical expert regarding all Tempus oncology test offerings.
  • Respond promptly and accurately to external medical information requests triaged by the customer success team.
  • Identify internal education gaps and develop educational presentations, live training modules, and utilize various training tools.
  • Continuously update stakeholders on relevant medical knowledge and develop market intelligence on competitor products.
  • Work effectively across multidisciplinary groups to provide comprehensive responses to medical/scientific inquiries.
  • Comply with medical information standard practices.
  • Contribute to the development of accurate marketing messages for various stakeholders.
  • Attend scientific meetings to stay updated on cancer genomic profiling and summarize learnings for internal teams.
Posted 12 days ago
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🔥 Research Associate - TIME
Posted about 1 month ago

📍 Northeast

🧭 Temporary

🔍 Healthcare

  • Regular travel required (up to 40%).
  • Bachelor's Degree and 3+ years of experience in oncology and/or clinical trials.
  • Deep understanding of study start-up.
  • Strong persuasive and motivational skills.
  • Proven track record of high performance standards.
  • Highly organized and attention to detail.
  • Ability to listen and develop strong relationships.
  • Advanced written and oral communication skills.
  • Superior analytical and problem-solving skills.
  • Persistent with a strong appetite for success.

  • Primary point of contact for research teams regarding TIME trial activities.
  • Maintain touch points with targeted accounts (2x per month per site).
  • Build relationships with key client stakeholders.
  • Draft and execute strategic operational plans for JIT standards.
  • Oversee processes in the operational plan.
  • Provide ongoing education about clinical trials.
  • Participate in research steering committees.
  • Collaborate with various teams to execute key deliverables.
  • Assist in creating innovative tactics and strategies to ease site burden.
  • Attend approved conferences.
  • Administer activities related to the responsibilities.

LeadershipProject CoordinationProduct OperationsCross-functional Team LeadershipOperations ManagementStrategyCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsTime ManagementWritten communicationRelationship building

Posted about 1 month ago
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🔥 TIME Clinical Research Coordinator
Posted about 2 months ago

📍 Unincorporated Los Angeles

🔍 Healthcare and clinical research

  • Candidate must have a Bachelor’s degree in Life Sciences or a health-related field.
  • 2+ years of clinical research experience in an oncology setting.
  • Knowledge of current FDA regulations, Good Clinical Practices (GCP's), and HIPAA.
  • CCRC preferable.
  • Strong planning and project management skills.
  • Excellent organization and communication skills with high attention to detail.
  • Proficiency with EDC systems and database management.
  • Proficiency with MS Office applications (Word, Excel, PowerPoint).

  • Educate and provide status updates to physicians and research staff regarding clinical trials in the TIME program portfolio.
  • Oversee the Tempus generated patient matches and maintain the patient tracker.
  • Screen potential study participants for available TIME trials.
  • Prepare rapid study activations for just-in-TIME trials and assist as needed during start-up.
  • Ensure all clinical trial data is entered into electronic data capture (EDC) systems efficiently.
  • Participate in research meetings and ensure startup timelines are met.
  • Create site support tools and TIME trial related communications.

Project ManagementProject CoordinationCommunication SkillsAnalytical SkillsCollaborationMicrosoft ExcelProblem SolvingMicrosoft OfficeAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communicationMultitaskingDocumentationMicrosoft Office SuiteMS Office

Posted about 2 months ago
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