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The Associate Director of Regulatory Affairs at Tempus will develop and implement regulatory strategies for medical devices. Responsibilities include leading submissions to regulatory authorities, ensuring compliance with various frameworks, and creating documentation needed for applications. The role entails collaboration with scientists, engineers, and legal teams, requiring strong leadership and project management skills.
Seeking a Senior Medical Science Liaison to support commercial, research, and educational objectives in oncology. Responsibilities include educating healthcare providers, organizing medical advisory boards, and providing scientific education. Requires advanced scientific or medical degree with KOL relationships in oncology.
The Sr. Manager, Commercial Learning & Development will develop and implement training programs for the sales teams, focusing on new hires and ongoing training. Responsibilities include coordinating training efforts, content creation, and providing feedback to sales management to enhance team performance.
The Precision Medicine Program Director will focus on identifying strategic account targets for Tempus offerings, providing solutions to healthcare professionals, and leading contracting efforts. The role involves analyzing competitive landscapes, collaborating with cross-functional teams, and driving sales processes while embodying the company culture.
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.
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