Tempus

Director, Epidemiology & Methodological Innovation

Tempus$170K — $230K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • PhD (preferred) or PharmD in Epidemiology, Biostatistics, Health Economics, or a related quantitative field.
  • 7+ years in HEOR/RWE, with at least 3 years in a leadership role.
  • Deep expertise in oncology is required.
  • Track record of developing or implementing advanced methods related to epidemiology.
  • Advanced skills in R or SAS, with experience in handling complex real-world data.
  • Exceptional communication skills in translating methodologies for executives.
  • Experience leading and mentoring teams in a high-growth environment.

Responsibilities

  • Lead the development of novel Real-World Evidence (RWE) methodologies.
  • Oversee end-to-end execution of retrospective database analyses as primary architect of study protocols.
  • Advise biopharma clients on innovative study designs as a subject matter expert.
  • Collaborate with business development to identify and tackle complex client challenges.
  • Bridge Data Science, Biostatistics, and Product teams to productize novel methods.
  • Ensure all research adheres to regulatory and ethical standards, delivering high-quality outcomes on time.

Benefits

  • Full range of benefits including medical and other healthcare options.
  • Incentive compensation and potential for stock options.
  • Professional development opportunities to enhance career growth.
Full Job Description
The Director of Epidemiology & Methodological Innovation will lead high-impact research for Tempus's biopharma partners, sitting at the intersection of traditional outcomes research and cutting-edge data science. This is a high-visibility, client-facing role within the Data Business. You won't just apply existing frameworks; you will develop and validate novel epidemiological methods to unlock the full potential of Tempus's multimodal datasets. The ideal candidate is a scientific visionary who can translate complex, non-linear data into regulatory-grade insights that accelerate drug development and improve patient outcomes.

Key Responsibilities
  • Methodological Innovation: Lead the development of novel approaches for RWE, including the use of external control arms (ECA), causal inference in high-dimensional data, and the integration of longitudinal clinical data with molecular/genomic signatures.
  • Research Design & Implementation: Oversee the end-to-end execution of retrospective database analyses. You will act as the primary architect for study protocols, ensuring they push the boundaries of current HEOR/RWE standards while maintaining scientific rigor.
  • Scientific Thought Leadership: Serve as a subject matter expert for biopharma clients, advising them on "first-in-kind" study designs. You are expected to contribute to the broader scientific community through high-impact publications and presentations at conferences like ISPOR, ICPE, and ASCO.
  • Client Strategy & Partnership: Partner with Key Account Directors and Business Development to identify opportunities where novel methodology can solve "unsolvable" client problems (e.g., rare disease characterization or complex biomarker validation).
  • Cross-Functional Synergy: Bridge the gap between Data Science, Biostatistics, and Product teams to productize successful novel methods, ensuring they are scalable across the Tempus ecosystem.
  • Project Management & Quality: Ensure all innovative research meets stringent regulatory and ethical standards (e.g., GEP, HIPAA), delivering high-quality results on timelines that match the pace of the biopharma industry.


Qualifications
  • Education: PhD (preferred) or PharmD in Epidemiology, Biostatistics, Health Economics, or a related quantitative field.
  • Experience: 7+ years in HEOR/RWE, with at least 3 years in a leadership capacity.
  • Deep expertise in oncology is required.
  • Methodological Mastery: Proven track record of developing or implementing advanced methods (e.g., target trial emulation, propensity score applications in complex cohorts, or machine learning-augmented epidemiology).
  • Technical Proficiency: Advanced skills in R or SAS. Experience working with "messy" real-world data (EHR, claims, and/or genomic data) is essential.
  • The "Consultant" Mindset: Exceptional ability to walk into a room of biopharma executives and simplify complex methodological hurdles into a clear strategic roadmap.
  • Leadership: Demonstrated experience mentoring junior scientists and leading cross-functional squads in a fast-paced, high-growth environment.


CHI: $170,000-$230,000
NYC/SF: $180,000-$250,000
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.

About Tempus

Tempus is a technology company that has built an operating system to battle cancer. The company enables physicians to deliver personalized cancer care for patients through its interactive analytical and machine learning platform. Tempus provides genomic sequencing services and analyzes molecular and therapeutic data to empower physicians to make real-time, data-driven decisions. The company also offers research services to enable discovery of new therapeutic targets and clinical services that support clinical trial design and monitoring. Tempus was founded in 2015 by Eric Lefkofsky and has raised over $8 billion in funding to date.
Learn more about Tempus
Size
1,001 employees
Industry
Founded
2015

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