Ro is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possible. Ro is the only company to offer nationwide telehealth, labs, and pharmacy services. This is enabled by Ro's vertically integrated platform that helps patients achieve their goals through a convenient, end-to-end healthcare experience spanning from diagnosis, to delivery of medication, to ongoing care. Since 2017, Ro has helped millions of patients in nearly every single county in the United States, including 99% of primary care deserts.
Ro is consistently recognized as a top workplace in Health Care, in New York, and for Women and Parents—earning more than 20 honors from Fortune, Great Place to Work, and PEOPLE since 2021. In 2025 alone, we ranked top 5 among medium workplaces in Health Care and New York, and top 50 nationwide.
We’re hiring a Senior Clinical Data Analyst to join Ro’s Scientific Affairs team—a small, high-impact group of physicians, scientists, and data experts shaping how clinical credibility is built in modern healthcare.
This is not a back-office analytics role. You’ll sit at the intersection of science, data, and storytelling, owning work that directly influences how millions of patients understand and trust their care. From substantiating marketing claims to generating real-world evidence for pharmaceutical partners to contributing to peer-reviewed publications, your work will be visible, strategic, and consequential.
You’ll collaborate closely with teams across Marketing, Legal, and Product (Digital and Physical), translating complex analyses into clear, credible narratives that stand up to scrutiny and resonate with patients. Alongside board-certified physicians, PhD-level scientists, and experienced health data analysts, you’ll bring rigor to everything from customer-facing claims to original research, clinical protocols, and conference submissions.
Whether you’re synthesizing data to guide evidence-backed content, helping shape a publication that advances the standard of care, or contributing to scientific and clinical conferences, you’ll see your work move quickly from insight to impact. If you thrive in ambiguity, love turning data into decisions, and want real ownership in redefining clinical trust at a fast-growing healthcare company, this role was built for you.
What You'll Do:
Analytical & Research Support (50%)
Bring analytical horsepower to Ro’s research, product, and thought leadership initiativesAnalyze internal data across patient outcomes, engagement, surveys, and program performanceSupport pharma partnerships, conference materials, executive readouts, and internal strategy with data-driven insightsWrite and optimize SQL queries on large clinical datasets in collaboration with data partnersTranslate complex analyses into clear, compelling summaries and visuals for technical and non-technical audiencesScientific Writing & Publication (30%)
Help define Ro’s external scientific voice through high-quality, publication-ready writingDraft and refine peer-reviewed manuscripts, conference abstracts, white papers, and scientific reportsConduct focused literature reviews to contextualize findings and support claims substantiationCollaborate on publication strategy, narrative framing, and conference planningEnsure scientific messaging is consistent, credible, and aligned across all external touchpointsResearch Operations & Claims Support (20%)
Own Ro’s research operations infrastructure and marketing claims pipeline end-to-end, ensuring every claim is scientifically sound, brand-aligned, and regulator-readyOwn research protocol submissions and revisions with multiple Institutional Review Boards (IRBs)Lead research study oversight Support the lead clinical reviewer as the single point of ownership for all claims requests, managing intake, prioritization, and executionPartner closely with Marketing, Legal, Medical, and Product to assess claim accuracy, feasibility, and evidence strengthMaintain and evolve a centralized claims system to ensure clear documentation, traceability, and fast turnaroundsIdentify and implement process improvements that streamline workflows without compromising integrity Help define and operationalize evidence tiers to balance speed, risk, and scientific rigor across campaignsWhat You’ll Bring to the Team:
Required Qualifications
B.S. in Healthcare, Biomedical Sciences or Related Field 3–5 years of experience in scientific research, healthcare consulting, medical affairs, or similar settingHigh comfort interpreting data and performing independent analyses (e.g. strong working knowledge of SQL)Demonstrated experience with scientific writing (e.g., publications, abstracts, reports)Strong project management and stakeholder communication skillsDetail-oriented and highly organized, with the ability to manage multiple prioritiesPreferred Qualifications
Master’s degree (MSc) or equivalent experience in Biostatistics, Quantitative Methods, or related disciplineWorking knowledge of statistics and research proposal and/or study design Experience working in a startup or digital health environmentFamiliarity with pharmaceutical, regulatory and legal considerations for marketing claims in healthcareExposure to peer-reviewed publication processes and conference submissionsWe've Got You Covered:
Full medical, dental, and vision insurance + OneMedical membershipHealthcare and Dependent Care FSA401(k) with company matchFlexible PTOWellbeing + Learning & Growth reimbursementsPaid parental leave + Fertility benefitsPet insuranceStudent loan refinancingVirtual resources for mindfulness, counseling, and fitness
We welcome qualified candidates of all races, creeds, genders, and sexuality to apply.