Staff Evidence Planning – Scientific Claims Manager

Verily

. Maintain the evidence-generation roadmap linking corporate strategy, product/commercial priorities, and market claims .

Posted 10/30/2026full-timeUnited StatesLead💰 $122,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in evidence strategy and real-world evidence (RWE) with a strong ability to translate competitive intelligence into prioritization decisions. Proficient in managing evidence dissemination pathways and engaging with stakeholders across medical affairs and commercial strategies.

Highest-signal resume keywords

Evidence StrategyReal-World Evidence (RWE)Research Prioritization FrameworkCompetitive IntelligenceHealth Economics

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Evidence DisseminationClinical Study DesignStatistical Analysis PlansQuantitative Scoring ToolsWeighted Rubrics

Soft Skills

Influence Without Authority

Tools & Technologies

Research Prioritization ScorecardSpreadsheet-Based Scorecards

Industry Keywords

Health SciencesHealth PolicyPublic HealthMedical AffairsLife SciencesDigital HealthAI-Enabled Clinical Products

About the role

Key responsibilities & impact

Maintain the evidence-generation roadmap linking corporate strategy, product/commercial priorities, and market claims
Translate competitive intelligence and outcomes benchmarking into evidence gaps and prioritization decisions
Operate the Research Prioritization Scorecard for ranking RWE, clinical studies, registries, and AI/data-science validation work
Advise study teams on evidence dissemination channels, including publications, congresses, preprints, KOL and medical affairs, sales enablement, payer/customer collateral, and executive readouts
Match claims to the most effective modality and audience
Support the manuscript publication end-to-end process
Partner with the Director of Evidence Generation and participate in the Verily EvGen Committee

Requirements

What you’ll need

7+ years in evidence strategy, HEOR, real-world evidence, medical affairs, or research operations, with direct exposure to how evidence decisions connect to commercial and product strategy
Demonstrated experience building or operating a research/evidence prioritization framework, scoring rubric, or portfolio-governance process across competing stakeholders
Working fluency in competitive intelligence for evidence and clinical claims, and ability to translate it into prioritization decisions
Deep familiarity with evidence dissemination pathways and their tradeoffs, including peer-reviewed publication and ICMJE norms, congresses, and commercial/sales enablement
Advanced degree in health sciences, health policy, public health, health economics, or a related field (preferred)
Background in a regulated health, life sciences, digital health, or AI-enabled clinical products environment (preferred)
Familiarity with IRB/human-subjects routing, statistical analysis plans, or clinical study design sufficient to engage credibly with methods-review bodies (preferred)
Comfort with quantitative scoring tools, weighted rubrics, and spreadsheet-based scorecards (preferred)
Strong influence without requiring formal decision authority
Must not require employer-sponsored work authorization now or in the future for employment in the United States

Benefits

Comp & perks

$183,000 bonus
Equity
Benefits