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The Regional Sales Manager will lead a Sales Team, manage business results, develop territory business plans, and create sales strategies within the New England region. Responsibilities include building customer relationships, overseeing sales activities, evaluating performance, and collaborating with cross-functional partners to achieve sales objectives and improve outcomes in the field of cancer genomics.
The RCM Specialist I will support accurate coding and billing processes for medical procedures, ensuring compliance with regulations. Responsibilities include coding for molecular oncology testing, managing patient billing worklists, resolving coding issues, and analyzing workflows for efficiency improvements.
The Solutions Director at Tempus is responsible for driving revenue growth for the TIME product line by cultivating partnerships with pharmaceutical and biotechnology companies. The role involves collaboration across teams, developing sales strategies, and maintaining relationships with R&D executives to align with client interests.
The Research Operations Associate will manage key sites in the TIME clinical trials network, serve as the primary contact for research teams, draft and execute operational plans, collaborate with various teams, educate on clinical trial access, and oversee site support staff. Responsibilities include building client relationships, identifying resource gaps, and contributing to marketing and sales efforts.
The Associate Director will lead Translational Research projects, manage a team of computational scientists, design and implement research studies, analyze data, and provide actionable insights for biopharmaceutical partners. Responsibilities include project management, collaboration with stakeholders, and continuous improvement of research methodologies.
The Associate Director, Translational Research/Real-World Evidence will lead projects using Tempus' data to support biopharmaceutical partners. Responsibilities include managing a team, implementing computational strategies, collaborating with stakeholders, overseeing deliverables, and continuously improving research quality to support drug development decisions.
The Senior Scientist in Life Science and Research Analytics will leverage a multimodal database for conducting complex computational analyses to provide actionable insights affecting patient care and drug development. Responsibilities include managing projects, leading teams, communicating scientific findings to stakeholders, and enhancing research methodologies.
The Outcomes Research Data Scientist will analyze Tempus data for real-world evidence (RWE) studies, interpret results, communicate findings, collaborate with various teams to enhance data quality, and ensure compliance with regulations. Candidates should possess experience in oncology, biostatistics, and handling observational healthcare data.
The Senior Scientist will lead and execute computational research projects in partnership with biopharmaceutical clients to drive precision medicine. Responsibilities include research design, strategic collaboration, and providing actionable clinical insights, while also supporting junior scientists and presenting findings to stakeholders.
The Senior Quality Assurance Specialist will ensure regulatory compliance within the RTP Laboratory, maintain CLIA certification, oversee QA activities such as training and document retention, conduct inspections, and engage in quality system improvements. The role requires interaction with lab personnel to address quality issues and implement corrective actions.
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