Senior Director, Research & Development
Company websitetempus.com (Tempus, opens in new tab)
Base salary $192K to $264K
Employer-published annual base salary, USD. Advertised base range in Chicago, IL
You apply on the employer's own site. Six Figure Work does not handle applications.
- LocationChicago, IL
- WorkplaceWorkplace not stated
- Status at last checkSource accepting applications when checked
- Last checked (1 h ago) · observed since
About this job
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.
Pay Range: $192,000-$264,000
The expected salary range 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.
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.
Source: Tempus on Workday · View original posting (opens in new tab)
This listingSenior Director, Research & Development$192K to $264K
Senior Director, Marketing - Germline Portfolio$190K to $260K
Senior Director, Research Strategy and Operations (Core Team Leader)$192K to $264K
Staff AI Scientist - AI Products / Life SciencesFrom $200K
Associate Director, Outcomes Research$150K to $200K
(Senior) Medical Science Liaison - North Central: North OH and Western PA (US, Cleveland, Toledo, Pittsburgh)$120K to $190K
(Senior) Medical Science Liaison - Mid South - GA, KY, or East TN$120K to $190K
Chart as a table
| Role | Published base |
|---|---|
| Senior Director, Research & Development (this listing) | $192K - $264K |
| Senior Director, Marketing - Germline Portfolio | $190K - $260K |
| Senior Director, Research Strategy and Operations (Core Team Leader) | $192K - $264K |
| Staff AI Scientist - AI Products / Life Sciences | From $200K |
| Associate Director, Outcomes Research | $150K - $200K |
| (Senior) Medical Science Liaison - North Central: North OH and Western PA (US, Cleveland, Toledo, Pittsburgh) | $120K - $190K |
| (Senior) Medical Science Liaison - Mid South - GA, KY, or East TN | $120K - $190K |
Observed changes
- First observed on the employer's board
- Began meeting the published-salary criteria
- Observed since
- Employer-stated posting date
- 2026-10-20
Where this pay comes from
Location as the employer wrote it: Chicago
Pay Range: $192,000-$264,000
- Method
- Employer text, read with fixed rules and re-verified
- Checked
- Rule set
- us-base-v2
The pay passage appears in the employer's own job text. Fixed, deterministic rules located it, and the passage below was checked against the stored copy of the posting.
What we verified
- The pay figures come from the employer's own listing, quoted exactly above.
- The pay is an annual base salary in US dollars with a minimum of at least $100,000.
- The role was publicly listed on the employer's job board when last checked.
We do not verify what the employer will actually offer, whether the employer is still recruiting for the role, or anything beyond what the employer published. Full methodology.
