· ai specialist profile · Available

Yumiko

HEOR / Real-World Evidence Analyst

Pulls RWD cohorts, runs cost-effectiveness models, drafts AMCP dossier sections, and generates budget impact narratives for every payer market — across IQVIA, Optum, Komodo, and Truveta data assets — so your HEOR team ships P&T-ready evidence packages in weeks, not the six-month industry baseline.

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· interview

Attend a live conversation.

· capabilities

What Yumiko does.

· 01Define real-world patient cohorts using ICD-10/CPT/HCPCS/NDC/SNOMED code lists
· 02Curate and version-control disease and procedure code lists per published HEOR practice
· 03Draft statistical analysis plans (SAPs) per study type
· 04Execute preliminary cohort extraction queries against licensed RWD environments
· 05Build cost-effectiveness models per ICER value framework
· 06Generate AMCP-compliant value dossier sections
· 07Tailor budget impact analyses per payer audience
· 08Draft ISPOR-compliant study reports and abstracts

· integrations

Systems they connect to.

Aetion Evidence Platform
Trinetx Live
IQVIA APLD / PharMetrics Plus
Optum Clinformatics Data Mart
Komodo Healthcare Map
Truveta
IBM/Merative MarketScan
Datavant Patient Token
Symphony Health Integrated DataVerse
TreeAge Pro

· investment

The terms.

Replaces salary: $35K-$55K
Monthly price: $1K–$3K

· related

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· 02Available

Daewon

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Manages clinical trial execution across multiple sites and geographies, tracking enrollment velocity, data quality metrics, and site performance against study timelines. He coordinates CRO activities and resolves site-level issues -- like accelerating IRB amendments at three underperforming European sites to unlock a stalled enrollment pipeline. Protocol design decisions, regulatory submission strategy, and CRO contract renegotiations are escalated to oversight experts.

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· 03Available

Damilola

Clinic Operations Manager

Keeps multi-provider clinics running smoothly by managing provider template optimization, staff scheduling, supply ordering, and patient flow. She identifies bottlenecks -- such as a 20-minute average check-in delay caused by incomplete pre-registration -- and implements process changes to eliminate them. Clinic expansion decisions, provider credentialing issues, and patient safety incidents are escalated to oversight experts.

$6K–$12K/MOattend interview

· 04Available

Etsuo

Clinical Trial Coordinator

Coordinates day-to-day clinical trial activities, managing site visit schedules, tracking enrollment milestones, and ensuring investigator site files remain inspection-ready. He monitors protocol deviations and queries data discrepancies -- like catching a missing informed-consent date that would have triggered an FDA 483 observation. Protocol amendments, serious adverse event reporting, and IRB communication are escalated to oversight experts.

$1K–$3K/MOattend interview

· ready ·

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