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Lead the development and commercialization of clinical assay projects, ensuring alignment with strategic goals, budget adherence, and timely delivery while managing risks and communication with stakeholders.

As a Senior Quality Engineer, you will lead verification and validation of medical device systems, conduct risk assessments, and ensure regulatory compliance, particularly in relation to FDA and quality control standards while collaborating with cross-functional teams.

The Medical Science Liaison will support Tempus by educating healthcare professionals on oncology products and gathering insights for future developments, focusing on molecular oncology and genomic profiling.

Responsible for managing all data management activities for clinical studies, including data collection, cleaning, reporting, and validation, while ensuring regulatory compliance and quality data delivery.

The role involves working with precision medicine technology to deliver insights to physicians, enhancing patient treatment decisions.

Lead statistical analysis for clinical studies in oncology and cardiology, provide project leadership, and mentor junior biostatisticians while ensuring regulatory compliance.