Tempus

Data Scientist II, Real World Evidence, Life Sciences R&D

Tempus • $110K — $150K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in epidemiology, biostatistics, data science, public health, or related field, or Master's with 2+ years experience.
  • Proficient in observational real-world healthcare data and survival analysis methodologies.
  • Expertise in R, SQL, and machine learning, especially using LLM coding assistants.
  • Strong client communication skills with experience tailoring messages for diverse stakeholders.
  • Excellent project management skills with the ability to thrive in dynamic environments.

Responsibilities

  • Lead observational studies utilizing real-world clinical data to derive insightful endpoints.
  • Collaborate with pharmaceutical partners to execute comprehensive RWE research plans.
  • Stay updated on advancements in real-world methodologies and oncology guidelines, contributing reusable code and best practices.
  • Incorporate advanced AI tools, including LLMs, to enhance workflows for coding and analysis.
  • Interpret and communicate complex results of RWE analyses to technical and non-technical audiences.
  • Work collaboratively with product and data science teams to improve data quality and analytical practices.

Benefits

  • Comprehensive benefits package including medical and other forms of specialized health care.
  • Incentive compensation opportunities.
  • Access to restricted stock units.
  • Supportive work environment encouraging professional growth.
Full Job Description
We are seeking a highly motivated and solutions-oriented RWE Data Scientist II with experience and interest in oncology and epidemiological study design to join our team. This role requires the ability to lead observational studies, derive insights from complex real-world clinical data, implement advanced statistical methods, and leverage cutting-edge AI tools to scale tasks and augment insights. Key Responsibilities • Pharma Collaboration & Strategy: Partner with pharmaceutical collaborators to independently execute robust RWE research plans that leverage the Tempus multimodal platform to address key questions in trial design and outcomes research. • Real World Data Expertise: Lead the derivation of complex real-world endpoints using extensive coding, demonstrating deep comprehension of Tempus clinical and molecular data structures and complexity, while also serving as an expert on the methodological nuances and limitations of real-world data. • Methodology & Platform Contribution: Stay up-to-date on methodological advancements in real-world studies (e.g., causal inference, survival analysis) and oncology guidelines (NCCN and ongoing clinical trials) to contribute to reusable code, internal packages, and best practices that can be applied across multiple collaborations. • AI & LLM Innovation: Incorporate LLMs, agentic workflows and other AI tools into day-to-day workflows to accelerate code development, discovery, documentation, review, and insight generation. • Scientific Interpretation & Communication: Interpret results of RWE analyses to draw appropriate inferences based on study design/statistical methods, while also evaluating study limitations. Communicate complex methods and results clearly to both technical and non-technical stakeholders. Prepare and present internal reports, external-facing deliverables, and, where appropriate, manuscripts or conference materials. • Cross-Functional Collaboration: Collaborate with internal product, oncology, and clinical abstraction, and real-world data science teams to continually enhance Tempus data quality, products, and analytical best practices. Minimum Qualifications • Education: Education in epidemiology, biostatistics, data science, public health, or a related field, to the level of either: - PhD - Master's degree and 2+ years of additional work experience • Technical and Statistical Proficiency - Proficiency with observational real-world healthcare data, including analytical experience with time-to-event methodologies (survival analysis). - Proven expertise in executing RWD analytical studies. - Proficient in using R and SQL, especially statistical tools and packages. - Proficiency applying machine learning, LLM-based coding assistants (e.g., Claude Code, Copilot, Cursor) and agentic frameworks to support data analysis, code review, or scientific documentation workflows. - Adherence to good software engineering practices (version control, modular code, documentation). • Communication & Client Focus: Demonstrated experience interfacing with clients, showcasing adeptness in presenting and tailoring messaging to a variety of stakeholders. • Soft Skills: Excellent written and verbal communication skills with strong project management skills. Ability to thrive in a fast-paced, dynamic environment working with multi-disciplinary scientists on complex problems. Preferred Skillsets • Experience working with Pharma or drug development. • Experience in clinical trial design (particularly Phase II-III) in the clinical development space. • Analytical proficiency with claims, EHR, or registry data. • Practical experience configuring or adapting LLMs, or using related tools/frameworks, to support scientific work. • Knowledge of oncology guidelines (e.g., NCCN). • Experience with biomarker or molecular data (e.g., genomics). • Experience with cloud platforms such as AWS and/or BigQuery and/or Google Cloud Platform (GCP). #LI-DA1 CHI: $100,000-$140,000 NYC/SF: $110,000-$150,000 The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, 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

Similar Jobs

More Jobs at Tempus

More Pharmaceuticals & Biotech Jobs

Find similar Data Scientist II, Real World Evidence, Life Sciences R&D jobs: