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

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

SQLscientific writingdata analysisliterature reviewsresearch protocol submissionsproject managementstatistical analysisstudy designpublication strategydata visualization

Soft Skills

analytical skillscommunication skillsdetail-orientedorganizational skillsstakeholder managementcollaborationprocess improvementindependent analysisprioritizationstrategic thinking

Certifications

B.S. in HealthcareB.S. in Biomedical SciencesMaster’s degree (MSc) in BiostatisticsMaster’s degree (MSc) in Quantitative Methods