Senior Director, Research & Development

Tempus AI, Inc.; Chicago (IL); On-site; USD 173,000 - 245,000; Full time

Benefits offered by this job

Comprehensive benefits package

Incentive compensation

Restricted stock units

Job summary

Tempus AI, Inc. in Chicago is seeking a Senior Director of Research & Development to lead development programs of molecular diagnostics. This role demands strategic leadership across various functions ensuring inspection-ready product development.

The ideal candidate will have a PhD with 8+ years or a Master’s with 13+ years in the life sciences field, specifically in diagnostics. The position offers a competitive salary range of $173,000–$245,000 and comprehensive benefits.

Qualifications

• PhD with 8+ years of experience or Master’s with 13+ years in molecular diagnostics or related field.
• Experience leading design-controlled product development for diagnostics.
• Strong knowledge of IVD/CDx development and regulatory submissions.

Responsibilities

• Lead late-stage development and validation for molecular diagnostic products.
• Serve as a key partner to Regulatory, Quality, and other teams.
• Oversee documentation strategies to ensure inspection readiness.

Skills

Leadership

Regulatory submissions

Cross-functional team collaboration

Molecular diagnostics

Process improvement

Education

PhD in a related field

Master’s degree in a related field

Job description

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

Senior Director, Research & Development

This leader will drive complex development programs from concept through launch, partner across R&D and operational functions, and build scalable systems that enable high-quality, inspection-ready product development.

Responsibilities

• Lead late-stage development, validation, and launch readiness for molecular diagnostic products, including IVD, CDx, IUO, and LDT programs.
• Provide strategic and scientific leadership for design controls, validation planning and execution, design transfer, and post‑launch changes.
• Serve as a key cross‑functional partner to Regulatory, Quality, Clinical Lab Operations, Bioinformatics, Automation, Program Management, and Pharma Business Development.
• Drive regulatory submission support, including FDA, IVDR, MolDX, NYS, CAP, and other global or regional requirements.
• Oversee documentation strategy and development processes to ensure inspection readiness, consistency, traceability, and scalability.
• Lead complex issue resolution, including deficiency responses, non‑conformances, root‑cause investigations, and scope pivots.
• Advance continuous improvement initiatives across product development, including templates, risk‑based tools, project estimation, change management, and process standardization.
• Support external and partner‑facing development programs, including companion diagnostics and contractual assay development efforts.
• Mentor and develop a high‑performing team of scientists and documentation specialists.
• Contribute to resource planning, budgeting, staffing strategy, and organizational development within R&D.

Qualifications

• PhD with 8+ years of experience or Master’s degree with 13+ years of experience in molecular diagnostics, assay development, or a related life sciences field in a regulated environment.
• Deep experience leading design‑controlled product development for molecular diagnostics or sequencing‑based assays.
• Strong working knowledge of IVD/CDx development, validation, design transfer, and regulatory submissions.
• Demonstrated success working in regulated frameworks including FDA, IVDR, ISO 13485, QMSR, MolDX, and NYS.
• Track record of leading cross‑functional teams through complex technical and regulatory milestones.
• Experience building scalable processes, documentation systems, and development infrastructure in a fast‑paced environment.
• Strong leadership, communication, and organizational skills, with the ability to influence across technical and operational stakeholders.
• Strong people management experience, including hiring, mentoring, and leading teams through growth and change.

Highly Desirable

• Experience supporting audits, inspections, pre‑submissions, deficiency responses, and approval pathways.
• Experience with companion diagnostic developments, pharma partnerships, and external development programs.
• Experience with automation, LIMS, and 21 CFR Part 11 compliant software tools such as ELNs.

Impact in This Role

This role is critical to advancing Tempus’ regulated diagnostics portfolio by ensuring products are scientifically robust, operationally scalable, and developed with the rigor required for successful launch, regulatory approval, and long-term platform growth.

Salary & Benefits

Estimated salary range: $173,000–$245,000 (applicable if the role is performed from Illinois; may vary for other locations). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

Equal Opportunity Statement

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.