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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.

The Manager of Regulatory Affairs develops and leads regulatory strategies for medical devices, ensuring compliance with global regulatory authorities. This role involves submissions for FDA approvals, managing cross-functional teams, and aligning regulatory strategies with business objectives while maintaining communication with executive leadership.

The Regional Sales Manager will lead a sales team to exceed sales goals, develop regional business plans, manage relationships with key customers, and oversee sales strategies. The role requires frequent travel within the Mountain Region to ensure effective management and execution of sales initiatives.

The Project Director will lead cross-functional teams in oncology clinical research, managing project timelines, budgets, and regulatory compliance. Responsibilities include client collaboration, overseeing project deliverables, and ensuring proper training and resource allocation throughout the project lifecycle.

The Senior Project Director is responsible for leading cross-functional project teams in oncology clinical research studies. This role involves managing project scope, timelines, budgets, and regulatory compliance while providing mentorship and acting as the primary contact for clients. Additionally, they facilitate effective teamwork and ensure the delivery of project objectives within specified guidelines.

The Director of Alliance Management is tasked with building partnerships with pharmaceutical companies to enhance their research using Tempus products. Responsibilities include managing data operations, providing scientific support, improving client satisfaction, and addressing partners' needs by developing customized proposals and cross-functional collaboration.

As a Senior Quality Engineer, you will lead the verification and validation of medical device systems, develop compliance documentation, manage risk assessments, and provide guidance in Computer System Validation, ensuring adherence to FDA regulations and industry standards. You'll engage in collaborative efforts, supporting quality assurance processes and training team members.