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The Director of Biostatistics leads a team in clinical research, developing statistical plans, collaborating across departments, and ensuring regulatory compliance.

The Manager of Regulatory Submissions will lead regulatory strategies and submissions for global authorities, ensuring regulatory alignment with business goals while collaborating with cross-functional teams on medical devices.

Lead global regulatory strategy and submissions for medical devices and IVDs, including FDA and international authorizations. Partner with cross-functional teams to develop premarket and postmarket plans, ensure compliance with standards (e.g., ISO 13485, 21 CFR), and report to executive leadership. Manage regulatory lifecycle, change control, and documentation for AI/ML and genomics-related products.

Lead and build the indirect procurement function, developing strategies for spend categories, driving cost savings, and integrating AI tools.

The Director of Marketing will lead corporate narrative and AI-driven customer experiences, executing strategies and overseeing Pharma Services marketing.

The Key Account Director drives global account strategy, maintains relationships with pharmaceutical clients, negotiates contracts, and collaborates across teams to enhance Tempus' role in precision medicine.

Strategically lead VA enterprise sales to drive adoption of Tempus precision medicine portfolio. Own top-down relationships with C-suite, run contracting/RFPs, embed diagnostics into clinical workflows/EHRs, coordinate cross-functional teams, develop KOLs, track account KPIs, and execute territory plans to maximize market share.

Responsible for leading precision medicine initiatives within major health systems, driving strategic sales and deepening relationships with decision-makers to foster adoption of Tempus' diagnostic portfolio.

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.