Tempus
Tempus

60 Tempus Human Resources Manager Jobs Hiring Near You

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... Contribute to resource planning, budgeting, staffing strategy, and organizational development ...

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... Contribute to resource planning, budgeting, staffing strategy, and organizational development ...

... and scaling of Tempus' clinical Quality Management System (QMS) and team. Operating at the ... Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... Matrix-manage people and resources across engineering, product management, operational leads, and ...

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... Matrix-manage people and resources across engineering, product management, operational leads, and ...

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... Matrix-manage people and resources across engineering, product management, operational leads, and ...

$29/hr

... Tempus Unlimited. Actively participates as a member of the department leadership team in support of ... resource needs. * Manage escalated participant, surrogate, provider, and stakeholder issues and ...

Staff Product Designer

Chicago, IL · Hybrid

$125K - $175K/yr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... Manage and maintain precision in all communication; be a leader and proponent of disambiguation

... and scaling of Tempus' clinical Quality Management System (QMS) and team. Operating at the ... Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.

Staff Product Designer

Chicago, IL · On-site

$125K - $175K/yr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... Manage and maintain precision in all communication; be a leader and proponent of disambiguation

Product Director, Lab Systems

Chicago, IL · On-site

$170K - $220K/yr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... , or Asset Management platforms), ideally within a distributed physical and/or regulated ...

Tempus AI is seeking a Senior Associate to act as a strategic partner to the oncology and ... Use CRM reporting (Salesforce) to turn around ad-hoc requests from field sales and commercial ...

Tempus AI is seeking a Senior Associate to act as a strategic partner to the oncology and ... Use CRM reporting (Salesforce) to turn around ad-hoc requests from field sales and commercial ...

Showing results 41-60

Tempus Jobs Information

What is it like to work at Tempus?

Tempus is a data-driven healthcare technology company that prioritizes innovation and collaboration, fostering a culture of teamwork and continuous learning.

The company's structure is designed to facilitate interdisciplinary collaboration, with teams comprising experts from various fields, including medicine, engineering, and data science, working together to develop and implement cutting-edge technologies that improve cancer care and patient outcomes.

Working at Tempus may appeal to individuals who are passionate about using data and technology to drive meaningful change in healthcare, as the company offers opportunities for professional growth, a dynamic work environment, and the chance to contribute to a mission that has the potential to impact millions of lives.

What makes Tempus an attractive place to work?

Tempus is a leading healthcare technology company that leverages artificial intelligence to revolutionize cancer care and improve patient outcomes. The company's workplace is characterized by a culture of innovation, collaboration, and teamwork, with opportunities for employees to work on cutting-edge projects and contribute to groundbreaking research. By joining Tempus, individuals can pursue a career that combines technical expertise with a passion for improving healthcare, with opportunities for professional growth, skill development, and making a meaningful impact in the lives of patients.
Infographic showing various Human Resources Manager job openings at Tempus in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 48% Physical, 6% Hybrid, and 46% Remote job distribution.

Senior Director, Research & Development

Tempus

Chicago, IL • On-site

$173K - $245K/yr

Full-time

Re-posted 2 days ago


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
Passionate about advancing precision diagnostics and regulated assay development?
Tempus is seeking a Senior Director, Research & Development to lead late-stage assay and product development across molecular diagnostics, with a focus on design-controlled IVDs, CDx, IUOs, LDTs, assay transfer, and process excellence. 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.
What You'll Do
  • 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 teams 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.
$173,000-$245,000
The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). 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.
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.