Search the 18 jobs at Tempus AI

The Senior Scientist will lead analytical projects to enhance the Tempus drug R&D platform, utilizing applied machine learning and generative AI to analyze complex data sets. This role involves collaborating with various teams, driving innovation, and effectively communicating insights to facilitate cancer precision medicine.

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 Associate Director will lead a team in conducting research projects using Tempus’ data to support drug discovery for biopharmaceutical partners. Responsibilities include implementing research studies, analyzing data, collaborating with stakeholders, and managing research projects to improve patient outcomes.

The Regional Sales Manager will lead a sales team in the New England region, focusing on exceeding sales goals for Tempus’s products. Responsibilities include creating and executing business plans, managing sales activities, developing customer relationships, and overseeing the performance of Clinical Account Executives. Frequent travel is required to support the team in their territories.

The Area Vice President will lead multiple regional sales teams to achieve sales goals across Tempus's product portfolio, create and implement business plans, manage Regional Sales Managers, build key customer relationships, and drive strategic collaborations while overseeing financial objectives and team development.

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 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 Solutions Director will lead partnerships with pharmaceutical and biotech clients, meet revenue goals, and collaborate cross-functionally to support client R&D objectives. Responsibilities include negotiating contracts, cultivating executive relationships, and tracking progress against strategic goals while contributing to the development of Tempus' Life Sciences portfolio.

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.

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 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 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.

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.

Seeking a Senior Medical Science Liaison with expertise in molecular oncology and genomic testing to educate healthcare providers about Tempus assays and technologies. Responsibilities include regional expert support, education of healthcare providers, collaboration on research studies, and providing scientific education internally. Travel required up to 50%.

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 Research Operations Associate will serve as the main contact for research teams involved in the TIME trials, managing operational plans and ensuring compliance with Just-In-Time standards. This role involves collaboration with various teams, onboarding sites, providing education on clinical trials, and developing marketing materials while maintaining strong relationships with stakeholders.

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.

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.