Jobs / United States / Flatiron Health INC

Flatiron Health INC

Medical Director

Remote - US · Remote · US only Posted today

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Where you can work from

United States only

Based on the listing's location: Remote - US.

The company's headquarters is not the same as where you may work from. Visa sponsorship only matters if you would relocate; see below.

Visa sponsorship, if you would relocate

Sponsorship verdict

Sponsorship possible

One solid signal, not two. Worth applying, and worth asking about sponsorship early.

  • Employer is on a government sponsor recordThe US Department of Labor certified 14 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Employer is on a government sponsor record
The US Department of Labor certified 14 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. Source: LCA disclosure data (US Department of Labor (OFLC)).
No salary bar for this route
H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.

US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

About the role

Reimagine the infrastructure of cancer care within a community that values integrity, inspires growth, and is uniquely positioned to create a more modern, connected oncology ecosystem. We’re looking for a Medical Director to help us accomplish our mission to improve and extend lives by learning from the experience of every person with cancer. Are you ready to be the next changemaker in cancer care? A note on level: We're open to candidates at the Associate Medical Director or Medical Director level depending on experience and scope of prior ownership in precision medicine. What You'll Do Flatiron Health is looking for a data-and technology-oriented clinician with oncology subject matter expertise who is passionate about real-world evidence (RWE) accelerating progress against cancer. You will be part of the Global Research Oncology team that operates across the US, UK, Germany, and Japan. In this role you will collaborate with a cross-functional team of oncologists/clinicians, data scientists, epidemiologists, software engineers, product managers, account directors, and clinical data specialists to help develop, commercialize, and deliver our oncology research data and services leveraging a breadth of tools, including artificial intelligence. You will serve as a core medical resource with a particular focus in precision medicine and cancer genomics. You will also help biopharma clients apply clinical and molecular use cases across the full R&D lifecycle—from early pipeline discovery through post-market clinical development. In addition you will: • Clinical Oncology & Precision Medicine RO Expert: Serve as a core medical expert unblocking high-volume, custom data requests across oncologic diseases including rare tumor types and complex, multi-omic biomarker profiles. Flexibly pivot across oncologic disease areas to scope, design, and clinically validate custom datasets and analyses for our biopharma partners. • Translational Oncology & Discovery Partner: Partner with clients early in their R&D lifecycle to show how clinical-molecular datasets can fuel target discovery, characterize novel biomarker-defined cohorts, evaluate tumor biology, and guide combination therapy approaches. Help researchers validate preclinical hypotheses in real-world cohorts and explore clinical trial findings via reverse translation. • Clinical Development Translation: Apply clinical development and trial design principles to help biopharma clients bridge the gap between traditional clinical endpoints and real-world evidence (RWE). Help clients understand how real world data can support external control arms, historic cohorts, or synthetic control designs for niche or rare trial populations. • Commercial Pre-Sales & Scoping Subject Matter Expert: Proactively provide clinical and molecular data expertise to support teams during pre-sales, client scoping, and solution building utilising internal or off-the-shelf external AI tools. Partner with scientific and commercial leaders to translate a client’s clinical development planning, target validation, or complex inclusion/exclusion criteria into precise data specifications across our various data assets. • Cross-Functional Solutioning: Partner closely with matrixed project teams to apply established clinical-molecular frameworks to complex dataset deliveries and custom client requests. • Internal Capability Building: Support the development of internal training resources and clinical documentation to help upskill delivery teams on rare biomarker cohorts and molecular data structures. • Scientific Contribution: Participate in research study projects requiring physician expertise with support from senior RO leaders, including presenting or speaking at scientific conferences. Who You Are You're a kind,

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