Hybrid Senior Clinical Data Analyst, Scientific Affairs

at Ro

• Job title: Senior Clinical Data Analyst, Scientific Affairs
• Job type: Full Time
• Experience level: Senior
• Salary: $121,100 - $140,500 per year
• Degree requirement: Bachelor's Degree
• Tech skills: SQL
• Location requirements: Hybrid, New York City, United States

About the role

• Senior Clinical Data Analyst at Ro, shaping clinical credibility through data analysis and storytelling. Collaborating across teams to enhance patient understanding and trust in healthcare.

Responsibilities

• 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
• 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
• 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 implement process improvements that streamline workflows without compromising integrity
• Help define and operationalize evidence tiers to balance speed, risk, and scientific rigor across campaigns

Requirements

• B.S. in Healthcare, Biomedical Sciences or Related Field
• 3–5 years of experience in scientific research, healthcare consulting, medical affairs, or similar setting
• High 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 skills
• Detail-oriented and highly organized, with the ability to manage multiple priorities
• Master’s degree (MSc) or equivalent experience in Biostatistics, Quantitative Methods, or related discipline (preferred)
• Working knowledge of statistics and research proposal and/or study design (preferred)
• Experience working in a startup or digital health environment (preferred)
• Familiarity with pharmaceutical, regulatory and legal considerations for marketing claims in healthcare (preferred)
• Exposure to peer-reviewed publication processes and conference submissions (preferred)

Benefits

• Full medical, dental, and vision insurance + OneMedical membership
• Healthcare and Dependent Care FSA
• 401(k) with company match
• Flexible PTO
• Wellbeing + Learning & Growth reimbursements
• Paid parental leave + Fertility benefits
• Pet insurance
• Student loan refinancing
• Virtual resources for mindfulness, counseling, and fitness