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Associate Director, Outcomes Research

Role overview

Qualifications

  • PhD, PharmD, or Masters degree in Epidemiology, Biostatistics, Health Economics, or a related quantitative field
  • 7+ years in HEOR/RWE, with at least 3 years in a leadership capacity
  • Deep expertise in oncology
  • Advanced skills in R or SAS

Responsibilities

  • Oversee the end-to-end execution of retrospective database analyses and act as the primary architect for study protocols
  • Serve as a subject matter expert for biopharma clients and contribute to high-impact publications
  • Partner with Key Account Directors to identify opportunities for innovative methodologies
  • Manage a small team of outcomes research scientists, providing guidance on analytical projects

Key facts

  • Remote from: United States
  • Full time
  • Senior (5-10 years)
  • Research Associate
  • English

Hard skills

Other skills

  • Consulting
  • Quality Assurance
  • People Management

About the company

Ambry Genetics logo

Ambry Genetics

Biotechnology

Ambry Genetics is a company built by scientists, genetic counselors and physicians, dedicated to leading the clinical genomic diagnostic industry. Ambry boasts the largest genetic sequencing lab in the world; is CAP-accredited, CLIA-licensed and, as part of the Konica Minolta family, has access to the most complete suite of diagnostic technology in the world. Ambry Genetics'​ scope of clients includes some of the world's most respected academic institutions, pharmaceutical companies and leading treatment hospitals. Our experience, technology and dedication to science make us a trusted source for all clinical genetic testing, and an ideal partner for developing precision medicine solutions. Patients are at the core of everything we do, which is why Ambry partners with several non-profit organizations so that we can help both patients and clinicians alike find answers. Hiring Fraud Alert: Ambry/REALM IDx has received reports of employment scams in recent months that seek financial commitments, or requests personal information from job candidates. Unsuspecting job seekers have reported receiving unsolicited contacts by phone, email or text from individual(s) posing to be or represent Ambry/REALM IDx recruiter(s). If you’ve experienced either of these scenarios, please visit this page to learn more about hiring fraud: https://consumer.ftc.gov/articles/job-scams. Or visit https://realmidx.com/careers/recruitment-fraud-alert/ to learn more about our policy on recruitment fraud. You can confirm the legitimacy of a job posting by viewing our current open roles at https://realmidx.com/careers/.

Company details

Company typeSME
IndustryBiotechnology
Company size501 - 1000

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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.

The Associate Director will lead high-impact outcomes 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

  • 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, ISPE, 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).
  • 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.
  • Scientific Thought Leadership & Publication Strategy: Drive the strategy and roadmap for scientific dissemination. Lead the authoring and publication of high-impact peer-reviewed manuscripts, abstracts, and conference presentations to demonstrate methodologic rigor and support broader healthcare evidence generation.
  • Cross-Functional Partnership: 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.
  • People Management: Manage a small team of outcomes research scientists, providing hands-on guidance on analytical projects and career development and growth.

Qualifications

  • Education: PhD (preferred), PharmD, or Masters degree 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 expertise: Proven track record of developing or implementing advanced analytical methods (e.g., target trial emulation, propensity score applications in complex cohorts, causal inference, or machine learning-augmented epidemiology) and creative problem solving.
  • 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 managing junior scientists and leading cross-functional squads in a fast-paced, high-growth environment

U.S. Pay Range: $150,000 - $200,000


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. 

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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