Senior Clinical Data Analyst, Scientific Affairs

Ro is a direct-to-patient healthcare company focused on providing effective care to patients. They are seeking a Senior Clinical Data Analyst to join their Scientific Affairs team, where the individual will analyze data, support scientific writing, and oversee research operations to ensure marketing claims are scientifically sound.

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
• Working knowledge of statistics and research proposal and/or study design
• Experience working in a startup or digital health environment
• Familiarity with pharmaceutical, regulatory and legal considerations for marketing claims in healthcare
• Exposure to peer-reviewed publication processes and conference submissions