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Senior Clinical Data Analyst, Scientific Affairs

Job in New York, New York County, New York, 10261, USA
Listing for: Roman Health Pharmacy LLC
Full Time position
Listed on 2026-05-14
Job specializations:
  • IT/Tech
    Data Analyst
Salary/Wage Range or Industry Benchmark: 121100 - 140500 USD Yearly USD 121100.00 140500.00 YEAR
Job Description & How to Apply Below
Location: New York

Overview

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 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 initiatives
  • Analyze internal data across patient outcomes, engagement, surveys, and program performance
  • Support pharma partnerships, conference materials, executive readouts, and internal strategy with data-driven insights
  • Write and optimize SQL queries on large clinical datasets in collaboration with data partners
  • Translate complex analyses into clear, compelling summaries and visuals for technical and non-technical audiences

Scientific Writing & Publication (30%)

  • Help define Ro’s external scientific voice through high-quality, publication-ready writing
  • Draft and refine peer-reviewed manuscripts, conference abstracts, white papers, and scientific reports
  • Conduct focused literature reviews to contextualize findings and support claims substantiation
  • Collaborate on publication strategy, narrative framing, and conference planning
  • Ensure scientific messaging is consistent, credible, and aligned across all external touchpoints

Research 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-ready
  • Own 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 execution
  • Partner closely with Marketing, Legal, Medical, and Product to assess claim accuracy, feasibility, and evidence strength
  • Maintain and evolve a centralized claims system to ensure clear documentation, traceability, and fast turnarounds
  • Identify and…
Position Requirements
10+ Years work experience
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