Search the 27 jobs at Tempus AI

The Biostatistician II will lead independent analyses supporting Medical Affairs at Tempus, working with clinical and molecular data to generate insights. Responsibilities include presenting findings, ensuring regulatory compliance, and participating in publications. Candidates should have a background in computational biology or biostatistics and skills in R and SQL.

The Manager of Strategic Partnerships will lead key partnerships and manage a team within Tempus' Customer Excellence division, driving strategic growth and overseeing customer relationships. Responsibilities include managing partnerships, team mentorship, liaising with internal teams, analyzing market trends, and achieving key performance metrics.

The Associate Director, Outcomes Research will design and implement research studies on late stage/commercial customers, analyze data to provide actionable insights, and collaborate with various stakeholders in order to improve biopharma outcomes. Key responsibilities include conducting observational studies, reporting results, and ensuring project management aligned with regulatory standards.

The Senior Scientist in Translational Research will design and execute research projects for biopharmaceutical partners, leveraging Tempus' platform for computational analyses. Responsibilities include managing projects, developing biomarkers, training junior scientists, communicating scientific findings, and enhancing research methodologies.

The Senior Alliance Manager is responsible for managing and growing partnerships with life sciences companies, ensuring client satisfaction and the effective execution of collaboration agreements. This includes regular stakeholder engagement, project progress monitoring, and internal coordination to drive value and strategic advancements in research and clinical programs.

The Senior Scientist will utilize Tempus' multimodal database for translational and real-world evidence research, integrating molecular and clinical data to provide actionable insights. Responsibilities include managing projects, training junior scientists, and communicating findings to stakeholders while staying updated on industry trends and improving research methodologies.

The Outcomes Research Data Scientist will analyze real-world evidence (RWE) data, conduct statistical analyses, and provide strategic recommendations based on research findings. The role involves collaborating with various teams to improve data quality and ensuring compliance with regulations.

Seeking an independent and motivated Science Writer to join the Scientific Communications team. Responsibilities include leading scientific/clinical manuscript preparation, internal R&D communication initiatives, collaboration on communication activities, and managing publication roadmaps.

The Associate Director of Regulatory Affairs will develop and lead regulatory strategies for medical devices, manage submissions, and ensure alignment with commercial goals. Responsibilities include addressing regulatory frameworks, collaborating with cross-functional teams, overseeing premarket and postmarket activities, and communicating with leadership and regulatory authorities.

The Senior Manager/Associate Director of Regulatory Affairs will develop and lead global regulatory strategies for medical devices, manage submissions and correspondence with regulatory authorities, establish regulatory processes, and ensure alignment of regulatory strategy with commercial goals while communicating with executives.

The Director of Alliance Management at Tempus is responsible for establishing and nurturing partnerships with life science companies to advance their research and clinical programs using Tempus products. This role focuses on understanding partner needs, coordinating data operations, and ensuring customer satisfaction while driving revenue and innovations in precision medicine.

The Senior Program Manager in Commercial Learning & Development will develop and implement training for sales teams at Tempus. Responsibilities include planning new-hire training, creating ongoing training modules, and collaborating with stakeholders to deliver impactful educational content.

As a Senior Solution Architect on the Lens team, you will collaborate with external partners, guiding them in using the Lens platform for data science applications in oncology. Responsibilities include customer training, data selection, and designing analytic workflows, while providing technical advice to clients.

The RWE Data Scientist will lead analyses of Tempus data for studies, derive real-world endpoints, interpret results, communicate findings to Pharma teams, collaborate with internal teams, and ensure compliance with regulations. They must have expertise in real-world data analytics and strong project management skills.

The Director of Research Data will lead the development of multi-modal molecular data models, integrating engineering and scientific strategies. Responsibilities include managing a team of scientists, implementing data workflows, and fostering collaboration across cross-functional teams to ensure quality data usage in clinical applications.

The Director of Business Development will focus on developing and expanding partnerships with academic and consumer companies, driving revenue for Tempus through contract negotiation, stakeholder engagement, and project management within the healthcare industry, particularly in the fields of research and multiomic testing.

The Regional Sales Manager will lead a regional sales team in the cancer genomics industry, focusing on achieving sales goals, developing business plans, and managing Clinical Account Executives across multiple states. The role involves strategic decision-making, building key customer relationships, and enhancing sales performance through training and market intelligence.

The Senior Associate, Pharmacovigilance is responsible for managing Serious Adverse Event (SAE) reports, developing safety management plans, conducting data entry in safety databases, and mentoring staff. This role requires strong compliance knowledge and the ability to generate regulatory reports while working independently and leading projects with minimal guidance.

The CRC Postdoctoral Research Fellow will study precision oncology in colorectal cancer using a major clinicogenomic database. The fellow will apply computational methods to analyze genomic, transcriptomic, histopathological, and clinical data and will develop independent research projects in genomic-guided medicine.

The Precision Medicine Program Director will identify strategic account targets, provide solutions to healthcare professionals, coordinate contracting, collaborate with teams, and analyze the competitive landscape while embodying Tempus's culture.