Health, Education & Government Life Sciences & Pharma Pharma Sales & Market Access

Payer & Formulary Access

Regulated development and commercialization journeys where clinical, quality, and market access align.

Magellan Rx Prime Therapeutics CVS Caremark OptumRx
Inside this journey
  1. Pre-Discovery

    Align the room on outcomes, decision process, and constraints before deeper discovery.

    1. Stakeholder Alignment

      Confirm decision roles, timeline, success metrics, and top risks across plan, medical, and employer stakeholders.

      Alignment Questions

      Start Here: Tell Us About Your World

      • Who are the people on your team we should know—titles, responsibilities, and who signs off on pharmacy changes?
      • How many lives does this formulary/benefit design cover today? Options: Under 50,000, 50,000–499,999, 500,000–1,999,999, 2,000,000 or more
      • Which model best describes how you currently purchase/manage pharmacy benefits? Options: Full-service PBM (traditional contract), Pass-through/transparent PBM, Vendor-managed formulary with carve-in/out, Self-administered with vendor partners, Other
      • Who is your incumbent PBM or vendor today and when does your contract renew?
      • What are the top three business goals driving your interest in exploring alternatives right now?
      • Which of the following best describes the current executive priority for pharmacy cost initiatives? Options: Urgent—executive mandate this quarter, High—strategic priority this year, Medium—monitoring and opportunistic, Low—no immediate urgency

      Are You Comfortable With the Numbers You're Being Told?

      • What if your reported net PMPM is masking a fast-growing specialty cost — how confident are you that your numbers show the whole truth? Options: Extremely confident, Somewhat confident, Doubtful, Not confident at all
      • What is your current overall net PMPM (or range) and how has it trended over the last 12–24 months?
      • What percentage of total drug spend is specialty today, and how quickly is that percentage changing? Options: Under 20%, 20%–35%, 36%–50%, Over 50%
      • Which therapeutic areas are driving the majority of your specialty spend right now? Options: Oncology, Autoimmune/Immunology, Hematology, Rare disease/Orphan, Hepatitis/CV/Diabetes, Other
      • How frequently do you reconcile actual manufacturer payments vs. reported rebate credits? Options: Monthly, Quarterly, Semi-annually, Annually, Rarely/never
      • When you look at your reconciliation process, where do you feel the most uncertainty—timing, granularity, auditability, or something else?

      Who's Really Calling the Shots?

      • What would happen to your implementation timeline if a clinical leader pushed back on a cost-saving formulary recommendation? Options: Timeline slips significantly, Minor delay, resolved internally, No impact, Unsure
      • List the stakeholders (plan leadership, medical directors, employer sponsors, procurement, legal) and the decision each controls.
      • Which of these stakeholders will need formal presentations or documented ROI to approve changes? Options: Pharmacy Director, Chief Medical Officer, Benefits/Compensation Lead, Finance/Controller, Procurement, Board/Trustees
      • What is your internal timeline for a vendor decision and contract execution? Options: 30 days, 60–90 days, 3–6 months, 6–12 months, Undetermined
      • What would success look like for each stakeholder group in the first 12 months (financial, clinical, operational)? Please be specific.
      • Across plan, medical, and employer stakeholders, what are the top three risks you worry will derail this initiative?

      Where Things Break Down — Tell Me the Stories

      • Tell me about a recent patient or provider story where prior authorization, access, or specialty routing failed — what happened and why did it matter?
      • How long does it typically take from a prior authorization initiation to final decision for specialty therapies? Options: Same day, 1–3 days, 4–7 days, 8–14 days, More than 14 days
      • How do providers and members usually communicate frustrations to you, and how often do these complaints reach executive leadership? Options: Daily, Weekly, Monthly, Rarely, Never
      • Which parts of your prior authorization workflow create the most manual work or error-prone handoffs? Options: Initial submission and documentation capture, Clinical review turnaround, Appeals and peer-to-peer, Member communications, EHR/Provider portal integration
      • What percentage of prior auths for specialty drugs are ultimately approved, denied, or redirected to different therapies? Options: Mostly approved (>80%), Mixed (50–80%), Many denied or appealed (<50%), Don't track reliably
      • How does it feel to your clinical team when throughput or denials spike—stress, burnout, defensiveness, or something else?

      Are Rebates Helping—or Hiding the Problem?

      • Could your current rebate structure be incentivizing higher list prices or shaping prescribing in ways that undermine net-cost goals? Options: Yes—likely, Possibly, Unlikely, No
      • How are rebates currently contracted (pass-through, spread, guaranteed net, hybrid)? Options: Pass-through/Transparent, Spread pricing, Guaranteed net PMPM, Hybrid/Complex, Unsure
      • How often do you receive line-level rebate detail tied to actual claims (not just lump-sum statements)? Options: Per claim/transaction, Monthly line-level, Quarterly aggregated, Annual summary, Never
      • Have you ever conducted an independent audit of manufacturer remittances or PBM rebate accounting? If so, what surfaced?
      • Which manufacturers or drug classes create the most complexity or dispute in rebate reconciliation?
      • What transparency or contractual protections would give you real confidence in rebate flows?

      If We Could Rebuild Your Formulary, What Would Change?

      • Imagine your formulary actually nudged prescribers and members toward the lowest-net-cost clinically equivalent option—what's the single biggest barrier to that today?
      • How is your formulary clinical governance structured (pharmacy & therapeutics committee frequency, membership, conflict-of-interest controls)?
      • What percentage of formulary decisions are driven primarily by clinical evidence vs. financial incentives vs. provider preference? Options: Mostly clinical evidence, Balanced clinical and financial, Mostly financial, Mostly provider preference
      • Where are you on biosimilar adoption for applicable therapies and what’s blocking faster uptake? Options: High adoption, Moderate, Low, Not using biosimilars
      • Do you currently use step edits, indication-based tiering, or value-based contracting? Please specify which and how effective they are.
      • If we proposed an evidence-based formulary change that reduced net cost but required a brief clinical exception pathway—how open would your medical leadership be? Options: Very open, Somewhat open, Hesitant, Not open

      What Would ‘Success’ Actually Look Like in 6–12 Months?

      • If you hit your target net PMPM reduction, but member complaints increased by 10%, would that be acceptable? Options: Yes, Maybe with mitigations, No, Depends on the nature of complaints
      • Which of the following KPIs must move for you to call the project a success? Options: Net PMPM / total cost, Specialty spend as % of total pharmacy, Prior authorization turnaround time, Provider satisfaction, Member access measures, Rebate reconciliation accuracy
      • What are your numeric targets or acceptable ranges for the top two KPIs (e.g., net PMPM reduction of X%, prior auth turnaround under Y days)?
      • Which reporting cadence and format would help you feel in control—weekly operational dashboards, monthly executive summaries, or quarterly deep dives? Options: Weekly dashboards, Bi-weekly updates, Monthly executive summaries, Quarterly deep dives
      • How will you verify clinical outcomes and member access are preserved while we chase cost improvements?
      • What level of financial guarantees or shared-savings arrangements would you consider necessary to move forward? Options: Full guaranteed net, Partial guarantees with shared savings, No guarantees, outcome-based metrics only, Undecided

      Data, Integrations, and Launch Readiness — How Close Are You?

      • If we needed end-to-end claims and clinical data tomorrow, how many of these feeds are currently available and production-ready: pharmacy claims, medical claims, enrollment, lab results, provider directory? Options: All available and ready, Most available with minor work, Some available, significant work needed, Few or none available
      • Which data formats or standards do you currently support for integrations? Options: X12 837/835/270/271, HL7/FHIR, CSV/SFTP, API-endpoints, Other
      • Who owns integrations, security, and data governance on your side (names/roles) and how fast can they be mobilized?
      • Do you have a provider-facing prior authorization portal today, and if so, how widely is it adopted? Options: Yes—widely adopted, Yes—limited adoption, No—manual processes, Planning to implement
      • What security or compliance requirements (SOC2, HITRUST, BAAs, state regulations) must vendors meet before going live?
      • What internal change-management resources (communications, training, provider outreach) can you commit to a deployment? Options: Dedicated team and budget, Some resources available, Minimal capacity, None—need vendor to lead

      Small First Steps: What Would You Let Us Try?

      • What's the smallest, least risky pilot you would approve that could prove value in 60–90 days? Options: A single therapeutic class, A subset of high-cost members, Rebate reconciliation audit, Prior authorization process redesign, Formulary tier change for a test cohort
      • If we ran a pilot, which success signals would make you ready to scale (quantitative thresholds and qualitative feedback)?
      • Who would need to sign off on a pilot and what approvals are required to begin?
      • What governance cadence would you prefer for reviewing pilot progress—weekly ops calls, biweekly steering, monthly executive review? Options: Weekly ops, Biweekly steering, Monthly executive, Ad-hoc
      • What are the most likely internal objections we should expect and who are the natural champions to help overcome them?
      • If the pilot shows early wins, how quickly could you expand scope or approve a commercial agreement? Options: Immediately, Within 30 days, 30–90 days, Longer than 90 days

      Final Check — Risks, Unsaid Concerns, and Next Steps

      • What's the single thing you haven't told any vendor yet that would change the conversation if we knew it?
      • Which risks keep you up at night about changing pharmacy partners—operational disruption, clinical quality, financial exposure, political resistance, or something else? Options: Operational disruption, Clinical quality, Financial exposure, Political/resistance, Other
      • What would you need from us in the next 7 days to feel this discovery was worth your time? Options: A tailored ROI model, Detailed project plan, References and case studies, A short pilot proposal, Security/compliance docs
      • Who else should join our next conversation to make progress and what would you like that meeting to achieve?
      • If we capture everything discussed and propose a focused next step, how would you prefer we deliver it—slide deck, live walkthrough with your data, or a brief written plan? Options: Live walkthrough with data, Slide deck and Q&A, Concise written plan, Other
    2. Current State Mapping

      Document formulary design, rebate flows, prior authorization workflows, specialty channels, and pain points that drive cost and access issues.

      Current State

      Start with the Paper Trail

      • To get us going: which single document or report best summarizes your current formulary and contracting setup? Options: Formulary policy PDF, Master rebate schedule, Claims summary report, Prior authorization SOP, No single source, Other
      • Walk me through how a new specialty drug typically gets from evaluation to coverage on your formulary — who touches it and in what order?
      • Which internal teams regularly update or approve formulary or clinical rules? Options: Pharmacy operations, Medical affairs, Clinical pharmacy team, Medical director, Finance/strategy, Legal/compliance, Other
      • How often do you publish formal formulary changes (e.g., quarterly, ad hoc)? Options: Monthly, Quarterly, Biannually, Annually, Ad hoc / as-needed
      • Who is your single point of contact for clarifying coverage decisions during vendor conversations?

      Where Money Disappears (and Why You Might Not Know)

      • When you trace net drug spend from gross ingredient cost to net PMPM, where are you most uncertain about the numbers? Options: Manufacturer rebates, Clinical rebates/adjustments, Specialty pharmacy fees, Direct and indirect remuneration (DIR), Provider-admin fees, Other
      • How do rebate flows move from manufacturer to payer in practice — direct payment, pass-through, aggregated remittance, or opaque reconciliations? Options: Direct to plan, Pass-through to plan, PBM-retained with reconciliations, Manufacturer clawbacks, Combination / hybrid, Not sure
      • Give an example of a recent reconciliation or audit finding that surprised you — what was the issue and impact?
      • How frequently do you reconcile rebates to claims and what percentage of reconciliations require manual adjustments? Options: Monthly, Quarterly, Annually, Ad hoc, No reconciliations
      • Which parts of the rebate lifecycle feel most opaque or risky to your finance team? Options: Contract terms/definitions, Measurement and attribution, Timing of remittances, Auditability, Data integrity, Other

      The Prior Auth Bottleneck — Who’s Really Getting Through?

      • Roughly what percentage of specialty prescriptions go through prior authorization today? Options: <10%, 10–25%, 26–50%, 51–75%, >75%, Unsure
      • When prior auth decisions are delayed, where is the harm felt most — patient adherence, provider churn, avoidable medical spend, or something else? Options: Patient adherence, Provider satisfaction/complaints, Medical spend (e.g., hospital/ER), Pharmacy leakage, Other
      • Describe your current prior authorization workflow from submission to decision — include tech platforms, average turnaround, and human handoffs.
      • Which of these best describes your prior auth operations today? Options: Fully manual with phone/fax, Hybrid (portal + manual review), Automated rules with human override, Third-party vendor handles most reviews, Not standardized
      • What are the top three reasons authorizations are appealed or escalated? Please give concrete examples.

      Specialty Channels: Who’s Actually In Control?

      • If I asked you: 'Are specialty pharmacy channels driving quality access or increased cost?' which half of that sentence feels more true for you today — and why? Options: More quality access, More increased cost, Balanced, Unsure
      • Which specialty fulfillment model do you primarily use? Options: Plan-owned specialty, PBM-owned specialty, External network specialty, Limited-home infusion partnerships, Multiple models / hybrid
      • How often do members use out-of-network specialty pharmacies, and what are the typical drivers? Options: Rarely, Occasionally, Often, Very often, Unsure
      • What controls do you have to route claims to preferred specialty channels (e.g., step edits, mandated dispensing site)?
      • Share a recent case where specialty channel choice materially affected cost or clinical outcome — what happened and what would you change?

      Formulary Logic: Comfortable or Compromised?

      • Do your current formulary tiering and utilization management rules consistently steer members toward the lowest-net-cost clinically equivalent option? Options: Yes, consistently, Mostly, Sometimes, Rarely, Never
      • How are clinical equivalence and therapeutic interchange decisions made and documented? Options: Clinical committee with minutes, Clinical team guidance, Vendor-provided rules, Ad hoc judgment by pharmacists, Not consistently documented
      • What percent of high-cost specialty fills could have been routed to a therapeutically equivalent lower-cost product (e.g., biosimilar) in the last 12 months? Options: <10%, 10–25%, 26–50%, 51–75%, >75%, Unknown
      • Where do you see the biggest tension between clinical guidance and financial steering in your formulary decisions?
      • If you could change one formulary rule or tier tomorrow, what would it be and why?

      Rebates: Transparent Partnership or Black Box?

      • Tell me honestly: when you look at rebate contracts, do you feel confident you’re capturing the full financial value for your members? Options: Completely confident, Mostly confident, Somewhat confident, Not confident, I don’t review contracts
      • Which rebate structures apply across your top 10 drugs by spend? Options: Fixed per-unit rebate, Performance-based rebates, Market-share/volume rebates, Flat percentage, No rebates, Combination
      • How are rebate liabilities and receivables modeled into your PMPM forecasts and budgets? Options: Included in PMPM forecast, Modeled separately, Not modeled reliably, Finance handles ad hoc
      • Have you experienced delays or shortfalls in expected rebate payments? If yes, describe impact and frequency. Options: Yes - frequent, Yes - occasional, Rarely, Never, Unsure
      • What visibility or reports would make rebates feel auditable and reliable to your team?

      Data Plumbing: Can You Trust What You're Seeing?

      • If a cost or utilization number looks wrong, how long does it take you to get a trustworthy answer? Options: Same day, 1–3 days, 1–2 weeks, More than 2 weeks, Never get a reliable answer
      • Which data feeds do you currently have into your analytics environment? Options: Real-time claims, Pharmacy claims batch, Medical claims, Rebate remittance files, Prior auth logs, Provider feedback, Other
      • What percentage of your formulary/rebate/prior auth decisions are informed by linked member-level claims versus aggregated reports? Options: Nearly all (90%+), Majority (60–89%), Some (25–59%), Rarely (<25%), Never
      • Describe a time data quality undermined a decision — what went wrong and how did you detect it?
      • Which data permission or access constraints slow down your ability to analyze savings/opportunity? Options: PHI restrictions, Vendor contract limits, Technical ingestion delays, Lack of IDs to link files, Internal governance approvals, Other

      Frontline Frictions: Provider and Member Voices

      • How often do providers call or complain about prior authorization complexity, and what do they typically ask for? Options: Daily, Weekly, Monthly, Rarely, Never
      • When members abandon prescriptions, do you have a consistent way to capture why — cost, access, confusion, or clinical reasons? Options: Yes - standardized reason codes, Partially captured, Anecdotal only, We don’t capture abandonment reasons
      • What feedback channels exist from providers and members back into formulary or prior auth design? Options: Provider portal comments, Member surveys, Support center logs, Advisory panels, None
      • Share a story where frontline feedback led to a policy change — what changed and how did outcomes improve?
      • Which stakeholder complaints do you feel most pressure to resolve quickly (e.g., C-suite, providers, large employer groups)? Options: C-suite/finance, Medical Director/CMO, Large employer clients, Provider networks, Member advocacy groups, Regulators

      Small Wins That Point to Bigger Levers

      • What recent small change (rule tweak, routing change, vendor tweak) produced outsized savings or fewer complaints?
      • Which operational change could be implemented in 60–90 days with minimal risk but likely measurable upside? Options: Formulary tier change, Prior auth criteria simplification, Route-to-preferred specialty, Add biosimilar default, Rebate contract renegotiation, Data reconciliation automation
      • If you had one dedicated analyst or project manager for 3 months, what would you task them to investigate first?
      • Who needs to be convinced internally for that short pilot to proceed, and what objection do you expect from them?
      • Finally, what success signal would make you say 'this is working' after a 3-month experiment (use concrete metrics if possible)? Options: Net PMPM reduction, Reduction in prior auth turnaround time, Increase in biosimilar adoption rate, Decrease in member complaints, Improved rebate realization, Other
  2. Outcome Discovery

    Define target financial and clinical outcomes, acceptance criteria (e.g., net PMPM reduction, prior auth turnaround), and measurable success signals.

    Discovery Questions

    A Quick Snapshot — where we start

    • Can you briefly describe your role and the population (lives) this formulary covers?
    • Which of the following best describes your organization today? Options: Large commercial health plan, Medicare plan, Medicaid plan, Large self-insured employer, TPA/ASO, Other
    • Roughly how many covered lives are in scope for the program we’d be discussing? Options: <50k, 50k–250k, 250k–1M, 1M–5M, >5M
    • Who on your team would be the primary owner of financial outcomes, clinical outcomes, and data/IT for this engagement? (names and titles are fine)

    If we stopped pretending 'good enough' is working

    • Where do you feel the largest disconnect exists between what your current PBM/benefit model promises and what you actually see in financial or clinical results?
    • Which outcomes consistently fall short of internal expectations? Options: Net PMPM, Specialty spend growth, Rebate reconciliation accuracy, Prior authorization turnaround, Biosimilar adoption, Member/provider satisfaction, Other
    • How long has this gap been present, and what have you already tried to fix it?
    • If you had to name the single most frustrating consequence of that gap—what is it and who feels it most?
    • How comfortable are your executive stakeholders (CFO/CMO/Benefits VP) with the current trajectory? Options: Very comfortable, Somewhat comfortable, Uncomfortable but tolerant, Actively concerned

    What if your target savings were non-negotiable?

    • What is the specific financial target you would call a success (e.g., net PMPM reduction, % rebate pass-through, total specialty spend reduction)? Please be explicit.
    • Which timeframe do you expect to see those financial improvements in? Options: 3 months, 6 months, 12 months, 18–24 months, Multi-year (3+ years)
    • What internal budget or ROI hurdle does any proposed solution need to clear to be approved? Options: Specific $ savings target, Percent of spend reduction, Payback period (months), C-level signoff regardless of ROI, Other
    • Which trade-offs are you willing to accept to hit financial targets (e.g., stricter utilization management, limited formulary breadth, slower prior auth turnaround)? Options: Stricter UM, Narrower formulary, Higher admin oversight, Phased member communications, No willingness to trade clinical access, Other
    • Tell us about a past initiative that hit financial targets but caused unforeseen problems—what happened and how did you recover?

    Clinical targets that actually change care — not just reports

    • Which clinical outcomes are non-negotiable for your team (examples: adherence, hospitalization avoidance, appropriate biosimilar substitution)? Options: Adherence for chronic meds, ER/hospital readmission reduction, Clinical guideline alignment, Biosimilar uptake, Appropriate specialist referrals, Other
    • What clinical KPIs does your medical leadership review regularly, and which ones keep them up at night?
    • How do you currently balance clinical quality vs. cost containment when they conflict? Please give a recent example.
    • What minimum clinical thresholds would cause you to pause or stop a program that is otherwise delivering on cost? Options: No thresholds; cost overrides, Small clinical decline tolerated, Specific metrics must hold (please specify), Clinical performance must improve
    • Which patient populations or disease areas are highest priority for improving clinical outcomes? Options: Oncology/specialty, Diabetes/CV, Mental health, Rheumatology/immunology, HIV/hepatitis, Other

    Acceptance criteria — what will make us say 'Yes, this worked'?

    • If we put a green light/red light definition on success, what three measurable signals would need to be true at 12 months?
    • Which of the following financial acceptance criteria matter most to you? Options: Net PMPM reduction, Gross-to-net reconciliation accuracy, Rebate per claim, Specialty spend % of total, Total cost of care impact
    • Which operational/experience criteria are must-haves (e.g., prior auth turnaround time, appeals rate, provider satisfaction)? Options: Prior auth turnaround, Appeals/overturn rate, Provider portal uptime, Member-facing denial clarity, Specialty pharmacy fulfillment speed
    • What statistical or reporting confidence level do you need to accept a result (e.g., p-value, margin of error, rolling 3-month trend)? Options: Rolling trend (3 months), Quarter-over-quarter, Year-over-year, Statistical significance required, Other
    • Who must sign off on the acceptance criteria once met (titles), and what documentation do they require?

    Signals, sources, and the data that will prove it

    • What primary data sources will we have access to for measuring outcomes (claims, lab results, EHR, member surveys, rebate statements)? Select all that apply. Options: Pharmacy claims, Medical claims, EHR/clinical data, Manufacturer rebate statements, Prior authorization logs, Member satisfaction surveys, Provider satisfaction surveys, Other
    • Are there known gaps in the data (e.g., delayed feeds, missing discipline codes, limited rebate granularity)? If so, what are they?
    • How frequently can these data sources be refreshed for measurement purposes? Options: Near real-time, Daily, Weekly, Monthly, Quarterly, Irregular / unknown
    • Which analytics or attribution methods do you trust today to tie intervention to outcome (e.g., difference-in-difference, matched cohorts, interrupted time series)? Options: Difference-in-difference, Matched cohorts, Interrupted time series, Regression modeling, Descriptive trend only, Unsure / need guidance
    • What level of transparency do you require on rebate flows and contract assumptions to validate net savings? Options: Full pass-through with reconciliation, Regular summary reports, High-level KPIs only, Independent audit rights required, Other

    What’s getting in the way — politics, people, and legacy systems

    • Which internal stakeholders are most likely to resist the changes needed to hit your targets, and why?
    • Have past vendor relationships failed because of governance breakdowns, integration issues, or misaligned incentives? Tell us one instructive story.
    • Which system integrations are historically the hardest at your organization (example: PBM to claims adjudication engine, PBM to EHR, rebate contract feed)? Options: Claims adjudication, EHR/clinical, Enrollment/eligibility, Specialty pharmacy fulfillment, Finance/AP, Other
    • How much internal bandwidth can you realistically dedicate to implementation and ongoing governance (FTEs, % of time)? Options: Dedicated team (3+ FTE), 1–2 FTEs, Fractional support (0.5–1 FTE), Ad hoc leadership only, Unsure
    • What red lines exist that would stop a program before launch (e.g., patient safety, regulatory concerns, vendor accreditation)?

    What would a credible 6/12/24‑month plan feel like?

    • If we agreed on targets today, what are realistic milestone outcomes at 6, 12, and 24 months (financial and clinical)? Please specify per interval.
    • Which quick wins could we aim for in the first 90 days that would build momentum? Options: Prior auth turnaround improvements, Formulary clean-up, Rebate reconciliation fixes, Specialty channel routing tweaks, Provider communications
    • What internal approvals and legal/commercial steps must complete before we can start work? Options: Legal contract, Data sharing agreement, Security review, Executive sponsor signoff, Other
    • How will you prefer progress to be reported (format and cadence)? Options: Weekly touchpoints, Biweekly steering, Monthly executive summary, Quarterly deep dives, Real-time dashboard access
    • Who should be in the room for milestone reviews so decisions can be made without delay?

    The emotional ledger — how this change needs to land with people

    • What are provider and member emotions you most worry about if utilization controls tighten or prior auth rules change?
    • How important is member/provider experience compared to immediate cost savings? Options: Experience prioritized over cost, Balanced equally, Cost prioritized over experience
    • Have you tested messaging or pilots to see how providers respond to stricter prior auth or formulary changes? What learned?
    • What support (education, scripts, escalation paths) would make providers feel respected during change? Options: Dedicated provider hotline, Pre-authorized exception paths, Clinical liaisons, Clear communication templates, Other

    Decision velocity — who, when, and what it will take to commit

    • Who are the decision-makers that must be convinced (titles), and what does each person care most about?
    • What timeline are you working toward for a vendor decision? Options: Immediate (30 days), Short (60–90 days), Quarterly cycle (3–6 months), Longer (6+ months)
    • What would constitute an unacceptable proposal — what must we avoid at all costs?
    • If everything aligned, what would be the earliest realistic start date for a program pilot? Options: Immediately, 1–2 months, 3–6 months, 6+ months
    • What additional information or artifacts can we prepare that would make your procurement and legal teams say ‘we can move forward’? Options: Sample contract language, Security attestation, Detailed SOW, Rebate modeling, Case studies with similar lives

    Closing the loop — next steps and what we’ll measure together

    • Which three metrics would you want included in a shared scoreboard from day one?
    • How would you like to validate initial results—pilot cohort, internal audit, or third-party review? Options: Pilot cohort, Internal audit, Third-party validation, Rolling phased validation, Other
    • What would make you feel confident enough after 90 days to expand scope or increase commitment?
    • Who on our team should be the direct point of contact, and who on your side will we coordinate with for data and approvals?
    • Anything we haven’t asked that would be critical for you in defining success?
  3. Solution Experience

    Walk through how our formulary, rebate strategy, and prior authorization operations deliver the customer’s target outcomes using their real data and scenarios.

    Experience Meetings

    • Data & Pre-Work Alignment
    • Current State & Consequence Confirmation
    • Outcome Definition & Future State Alignment
    • Live Solution Experience — Clinical, Formulary & Prior Auth Scenarios
    • Financial & Rebate Simulation, Tradeoffs, and Decision
    • Seller to produce a scenario summary report with screenshots, logs, and the exact data rows used for customer records.
    • Agree a single-sentence future state that all parties can validate against scenario outcomes.
    • Establish specific, measurable acceptance criteria and the data sources to verify them.
    • Confirm governance, reporting cadence, and sign-off owners for success validation.
    • Finalize KPI targets and acceptable thresholds and include them in the measurement plan.
    • Set up baseline KPI reports and schedule the first post-deployment verification window.
    • Identify governance attendees and schedule recurring KPI review meetings.
    • Recap Preconditions & Success Criteria
    • Prove the proposed future state through at least two real, customer-sourced scenarios.
    • Tie every step of the solution back to the verified customer problem and documented consequence.
    • Get explicit stakeholder validation (or documented exceptions) for each scenario outcome.
    • Document scenario outcomes, delta to baseline, and any config/policy exceptions identified during the walkthrough.
    • Introductions & Meeting Objectives
    • If exceptions found, owner to propose remediation/config options and estimated impact on KPIs.
    • Demonstrate financial proof (net PMPM change) tied to the validated scenarios and rebate mechanics.
    • Align on tradeoffs and operational requirements necessary to achieve projected savings.
    • Recap Validated Outcomes from Live Walkthroughs
    • Reach a clear decision to proceed to Solution Scope or define remaining open items and owners.
    • Deliver the final financial model workbook with scenario tabs and sensitivity results to the customer.
    • If proceeding, create a SoW/Scope draft that ties agreed modules, responsibilities, KPIs, and verification criteria to the proven scenarios.
    • If open items remain, list them with owners, expected resolution dates, and impact on the projected net PMPM.
    • Confirm all required data sets and artifacts are available or have a remediation plan.
    • Agree a concise, validated one-sentence current state that will be used in all subsequent sessions.
    • Establish owners and deadlines for missing data to enable the live walkthroughs.
    • Customer to deliver final claims extract (rolling 12 months), formulary file, PA logs, and rebate schedules by agreed date.
    • Seller analytics team to validate data ingestion and surface any anomalies within 48 hours.
    • Draft and circulate the one-sentence current state for stakeholder sign-off.
    • Restate One-Sentence Current State
    • Have a clearly supported, data-driven statement of consequence tied to the current state.
    • Agree which real-world scenarios will be used to prove the future state.
    • Secure stakeholder validation that the quantified consequences are accurate and urgent.
    • Analytics owner to produce a baseline metrics pack (net PMPM, utilization, PA turnaround) and circulate.
    • Customer to confirm final selection of 2–4 member/claim scenarios for live walkthroughs.
    • Flag any outlier claims or policy exceptions that require special handling during the experience.
    • Present Proposed One-Sentence Future State
    • Evidence Review: Utilization, Spend, and Workflow Metrics
    • Define Acceptance Criteria & KPIs
    • Confirm Scenario Context & Data Mapping
    • Rebate & Net-PMPM Simulation
    • Inventory of Received Artifacts
    • Scenario A — Formulary Decision & Claim Adjudication
    • Quantify Consequences (Cost, Delay, Risk)
    • Sensitivity & Tradeoff Analysis
    • Map Verification Signals & Data Sources
    • Validate/Produce One-Sentence Current State
    • Operational Impact & Transition Considerations
    • Gap List & Data Remediation Plan
    • Governance & Sign-off Process
    • Scenario B — Prior Authorization Workflow & Turnaround
    • Validate Consequences with Stakeholders
    • Decision & Next Steps to Solution Scope
    • Identify Priority Use-Cases to Demonstrate
    • Scenario C — Rebate Routing & Financial Reconciliation
    • Pre-work Confirmations & Next Steps
    • Validation & Forced Confirmation
  4. Solution Scope

    Define included modules (formulary management, rebate contracting, specialty pharmacy, prior auth), responsibilities, and verification criteria.

    Scope Configuration

    • Manage formulary coverage and tier placement
    • Negotiate and administer manufacturer rebate contracts
    • Process pharmacy claims adjudication
    • Operate provider prior authorization portal and decisions
    • Manage specialty pharmacy dispensing and fulfillment
    • Operate specialty patient access and hub services
    • Deploy step-therapy and quantity-limit utilization edits
    • Run biosimilar interchange and switching programs
    • Provide monthly drug utilization and cost reports
    • Administer rebate pass-through accounting and remittance
    • Run member medication adherence and clinical outreach
    • Operate member cost-transparency tools and estimators

    Scope Questions

    Manage formulary coverage and tier placement

    • Who will own ongoing formulary governance after deployment? Options: Customer pharmacy team, Vendor (full management), Shared governance (hybrid)
    • Which formulary model do you want implemented? Options: Open formulary, Closed formulary, Tiered with exclusions, Custom specialty carve-outs
    • What drug classes or therapeutic areas should be targeted first for redesign? Options: Specialty injectables, Oncology, Immunology, Cardiology, Multiple
    • How frequently should formulary tiering and clinical criteria be reviewed and updated? Options: Quarterly, Biannually, Annually, Ad-hoc per new launch
    • Are there mandatory excluded or protected drugs (e.g., state mandates, carve-outs)? List or describe.
    • What verification criteria will confirm the formulary module is configured correctly (e.g., correct tier mapping, clinical criteria applied)?

    Negotiate and administer manufacturer rebate contracts

    • Do you require vendor-led rebate negotiations or administration only? Options: Full negotiation + administration, Administration of client-negotiated contracts, Administration only with audit support
    • What rebate contract types should be supported in scope (select all that apply)? Options: Per-unit rebates, Gross-to-net adjustments, Performance-based / outcomes-linked rebates, Clawbacks & recoupments, Market-share guarantees
    • What reconciliation cadence do you require for rebate remittance and reporting? Options: Monthly, Quarterly, Semi-annual, Annual
    • Do you require transparent pass-through accounting and line-item visibility for each rebate? Options: Yes - full transparency, Partial transparency, No - aggregated reporting
    • Please describe any existing rebate agreements or legacy accrual practices that must be accommodated.
    • What acceptance criteria will validate rebate administration (e.g., reconciliation accuracy, timing of remittance, auditability)?

    Process pharmacy claims adjudication

    • Will claims adjudication be handled on our platform or integrated with your existing adjudication engine? Options: Vendor adjudication engine, Integrate with customer engine, Hybrid/parallel testing
    • What claim volumes should the adjudication flow be configured for (avg/month)? Options: <10k, 10k-100k, 100k-1M, >1M
    • Are there custom benefit rules, member-level overrides, or employer carve-outs that must be implemented? Options: Yes, No
    • What turnaround time SLA is required for claim processing and exceptions? Options: Real-time (<1s), Near-real-time (1-5s), Batch within 24 hours, Custom SLA
    • List data feeds and formats needed for adjudication (e.g., NCPDP, 835, 837), or leave blank to describe.
    • What verification checks will confirm adjudication is correct (e.g., claim pass rate, paid-claim sample audits)?

    Operate provider prior authorization portal and decisions

    • Do you require vendor-hosted prior authorization portal or integration with your provider portal? Options: Vendor-hosted portal, Integrate into existing provider portal, Both (redirect + API)
    • Which decisioning model do you prefer for prior auths? Options: Rules-based automated, Clinician review (nurse/pharmacist), Hybrid automated + clinical review
    • What PA turnaround times and SLAs are required for different categories (standard vs expedited)? Options: 24 hours, 48 hours, 72 hours, Same-day for urgent
    • Do you need real-time provider status updates, electronic submission (ePA), and integrations with EHRs? Options: ePA + EHR integration, Portal only, API-based submissions
    • Are there specialty or complex authorizations that require multi-step workflows (e.g., prior clinical documentation, case management)? Describe.
    • What acceptance criteria will validate PA operations (e.g., % auto-decisions, average decision time, provider satisfaction)?

    Manage specialty pharmacy dispensing and fulfillment

    • Do you want vendor specialty pharmacy services or coordination with external specialty pharmacies? Options: Vendor-operated specialty pharmacy, Network of external specialty pharmacies, Hybrid model
    • Which fulfillment capabilities are required? Options: Home delivery, Cold-chain management, Hub coordination, White-glove nursing support
    • What patient populations or therapy areas must be prioritized for specialty dispensing (e.g., oncology, rare disease)?
    • Are there existing specialty contracts, provider relationships, or distribution rules to maintain? Options: Yes - list/describe, No
    • What KPIs will confirm specialty dispensing readiness (e.g., fill turnaround, temperature excursion rate, adherence on specialty therapies)?
    • Do you require inventory visibility and reporting across specialty channels? Options: Yes - real-time dashboards, Periodic reports, No

    Operate specialty patient access and hub services

    • Should vendor operate patient access/hub services (benefit investigation, PAP assistance, financial support coordination)? Options: Full hub services, Limited support (benefit investigation only), No hub services required
    • Which hub capabilities are required at launch? Options: Benefits investigation, Prior auth support, Patient assistance program enrollment, Copay support
    • Do you need multilingual patient support or specialty nurse case management included? Options: Yes - multilingual, Yes - nurse case management, No special requirements
    • Are there manufacturer hub requirements or restrictions we must adhere to? Options: Yes - provide details, No
    • What success metrics will validate hub operations (e.g., time to benefit verification, PAP enrollment rate, patient satisfaction)?
    • Will data exchange with hubs require HL7/FHIR, secure SFTP, or API connections? Options: FHIR/API, SFTP, Portal/manual upload, Other

    Deploy step-therapy and quantity-limit utilization edits

    • Which classes should have step-therapy applied initially? Options: High-cost specialty, Certain brand classes, All brand-to-generic substitutions, Custom list
    • What tolerance for override/appeal volume do you expect and how should exceptions be handled? Options: Automated clinical override, Manual review by pharmacist, Provider appeal workflow
    • Do you require prospective DUR checks or real-time quantity limit enforcement at point of sale? Options: Prospective DUR + POS enforcement, Post-pay edits only, Both
    • Are there existing clinical guidelines or protocols to reference when building edits? Options: Yes - provide documents, No - vendor to recommend
    • What monitoring and rollback controls do you require for new edits (e.g., pilot cohorts, A/B test)? Options: Pilot rollout, Full rollout, Phased by line of business
    • What acceptance criteria will confirm edits are correctly deployed (e.g., reduction in inappropriate fills, override rate targets)?

    Run biosimilar interchange and switching programs

    • Do you want active biosimilar switching programs or passive formulary routing? Options: Active switching (member/provider outreach), Passive routing at adjudication, Both
    • Which biologic classes are highest priority for biosimilar adoption? Options: Insulin/GLP-1, Monoclonal antibodies, EPOs/HSCT agents, Other/Custom
    • Will you permit automatic substitution at pharmacy (interchange) or require provider notification/consent? Options: Auto-substitute permitted, Provider notification required, Provider consent required
    • Do you require metrics and reporting on biosimilar penetration and savings tracking? Options: Yes - monthly reporting, Quarterly reporting, No reporting required
    • Describe any regulatory, contractual, or clinical constraints that affect biosimilar switching in your population.
    • What success criteria will confirm the biosimilar program (e.g., adoption rate, net PMPM savings)?

    Provide monthly drug utilization and cost reports

    • Which recipients should receive monthly reports (e.g., CMO, pharmacy director, finance)? Options: Pharmacy director, Chief Medical Officer, Finance team, Employer benefits lead, All listed
    • What standard metrics must appear on the report (select all that apply)? Options: Net PMPM, Top 25 drugs by spend, Specialty spend trend, Rebate accruals, Utilization rates
    • Do you require drill-down capability to member-level or provider-level details? Options: Member-level, Provider-level, Aggregate only
    • What delivery format is preferred for reports (PDF dashboard, CSV export, BI dashboard)? Options: PDF summary, CSV/data extract, Interactive BI dashboard, All available
    • Are there specific timelines or governance meetings tied to the monthly reporting cadence? Options: Yes - monthly governance review, Quarterly review only, Ad-hoc
    • What acceptance criteria validate the report module (e.g., data freshness, reconciliation to finance)?

    Administer rebate pass-through accounting and remittance

    • Do you require full pass-through accounting with per-member attribution or aggregated remittance statements? Options: Per-member/pass-through, Aggregated remittance, Hybrid reporting
    • Which remittance cadence do you require for passing funds to the customer? Options: Monthly, Quarterly, On-reconciliation
    • Should vendor provide audit-ready ledgers and support third-party audits? Options: Yes - full audit support, Limited documentation, No
    • Are there multi-contract scenarios needing allocation rules (e.g., multiple plans under a customer, carve-outs)? Options: Yes - complex allocation, No - single contract
    • Please describe any legacy accruals, holdbacks, or disputed amounts that must be reconciled at go-live.
    • What verification criteria will confirm pass-through accounting is correct (e.g., sample reconciliations, GL tie-out)?
  5. Mutual Commit

    Finalize commercial and contractual terms, data access requirements, KPIs, and governance cadence for the engagement.

    Agreement Modules

    • Master Services Agreement (MSA)
    • Statement of Work (SOW)
    • Pricing & Commercial Schedule
    • Service Level Agreement (SLA)
    • Data Processing & HIPAA Business Associate Agreement (BAA)
    • Data Access & Integration Requirements
    • KPIs, Measurement & Governance Plan
    • Acceptance Criteria & Go/No-Go Signoff
    • Rebate Pass-Through & Reconciliation Schedule
    • Security & Compliance Attestation
    • Implementation & Onboarding Plan
    • Change Order & Scope Amendment Process
    • Payment Terms & Invoicing Schedule
    • Termination, Transition & Exit Plan
    • Audit Rights & Regulatory Cooperation
    • Subcontractor & Third-Party Consent
  6. Deployment

    Operationalize rollout with readiness checks, enablement, and outcome validation.

    1. Pre-Deployment Readiness

      Confirm data feeds, system integrations, provider portals, security controls, and responsible owners are in place for launch.

      Readiness Questions

      Starting Together: A Quick Snapshot

      • What's your title and the approximate population you manage (commercial lives / Medicare / Medicaid / ASO)? Options: Pharmacy Director, Chief Medical Officer, Benefits VP/Director, Other
      • What are the top 1–2 priorities for your pharmacy/benefits organization in the next 12 months? Options: Reduce net PMPM, Improve prior auth turnaround, Increase biosimilar adoption, Increase rebate transparency, Improve member/provider experience, Other
      • How would you describe your current relationship with your PBM(s) or vendors right now—mainly stable, fraying, or in transition? Options: Stable / highly functional, Some friction but manageable, Fraying / trust issues, Actively transitioning or RFP in flight
      • When you think about a successful partnership, which single outcome matters most to you personally? Options: Measured reduction in net PMPM, Fewer provider/member complaints, Faster prior auth turnaround, Clear, auditable rebate reporting, Improved clinical outcomes, Other
      • Tell us one recent win or one recent pain point that captures how your pharmacy program feels today.

      If You Could Turn the Tide Tomorrow, What Would Be Different?

      • Right now, what’s the one result you would trade everything else for if it meant solving it within 6 months? Options: X% net PMPM reduction, Eliminate specific rebate leakage, Cut prior auth turnaround by Y hours/days, Achieve Z% biosimilar conversion, Other
      • What specific financial and clinical targets would make you say the engagement was an unqualified success?
      • Which stakeholders must be visibly satisfied for this to count as success (select all that apply)? Options: Pharmacy Director, CFO/Finance, Chief Medical Officer, Employer Benefits Lead, Member Experience/Call Center Lead, Legal/Compliance
      • How would you like success to be measured and reported (frequency and format)? Options: Monthly dashboard, Quarterly executive review, Real-time KPI portal, Ad-hoc deep-dive reports, Other
      • If we achieved the financial targets but created marginally more provider work, would you consider that acceptable, or is provider burden a hard stop? Options: Acceptable if net savings significant, Acceptable with mitigation plan, Hard stop—provider burden cannot increase, Unsure

      Where the System Is Leaking Money and Trust

      • Which area feels most like a recurring source of waste, error, or frustration—formulary design, rebate reconciliation, prior auth, specialty pharmacy, or something else? Options: Formulary design, Rebate reconciliation, Prior authorization, Specialty pharmacy/channeling, Claims adjudication, Other
      • Can you give a concrete example (recent case or metric) where that problem cost you money or created member/provider escalation?
      • How confident are you in the accuracy and auditability of rebate flows and manufacturer payments today? Options: Very confident, Somewhat confident, Doubtful, We have no visibility
      • How often do prior auth delays lead to appeals, ER visits, or provider churn in your experience? Options: Frequently (weekly), Often (monthly), Occasionally (quarterly), Rarely/Never
      • Which drug categories drive the majority of your volatility and why (select all that apply)? Options: Oncology, HIV/Antivirals, Autoimmune/TSB, Specialty biologics, High-cost generics, Biosimilars, Other
      • How does this friction feel internally—annoying, urgent, politically risky, or existential? Options: Annoying/operational, Urgent/needs action, Politically risky, Existential/major financial risk

      Assumptions We're Both Making — Which Are Wrong?

      • What conventional wisdom about your PBM or the market do you suspect is wrong but haven’t had the space to test?
      • Which of these do you assume is true about your current arrangement: rebates equate to net savings, prior auth is mostly clinical, specialty routing is optimized, or something else? Options: Rebates = net savings, Prior auth is primarily clinical, Specialty routing maximizes value, Claims adjudication is unbiased, Other
      • How often do vendor contracts or PBM practices force trade-offs you privately disagree with (e.g., clinical vs. financial priorities)? Options: Always, Often, Sometimes, Rarely, Never
      • If we challenged one long-held assumption together, which one would you want us to examine first and why?
      • How comfortable are your internal stakeholders with surfacing uncomfortable truths about vendor performance? Options: Very comfortable, Somewhat comfortable, Hesitant, Not comfortable at all

      What Would Success Actually Feel Like for Your Team and Members?

      • Imagine it’s 12 months after go-live and you’re presenting results—what anecdote would you tell that proves we got it right?
      • Which member or provider experience improvements would matter most to your executives (select up to 2)? Options: Faster prescriptions filled, Fewer appeals, Clearer communications, Lower out-of-pocket cost, Fewer therapy interruptions, Other
      • What are the minimum quantitative thresholds (e.g., net PMPM, prior auth turnaround, biosimilar uptake) that would make you confident to expand the program?
      • Beyond numbers, what cultural or political signals would tell you this partnership is trusted and sustainable?
      • Which executive will sign off on expansion when those thresholds are met, and what do they care about most? Options: CFO/Finance, Chief Medical Officer, Head of Benefits/HR, CEO/President, Board/Trustees, Other

      Roadblocks You Can See Today — And the Ones You’re Not Saying

      • What internal obstacles (IT, legal, procurement, unions, budget cycles) are most likely to delay launch? Options: IT/data access, Legal/contracting, Procurement/RFP timing, Budget cycle/fiscal year, Stakeholder alignment/politics, Other
      • How ready are your systems to deliver the data we’d need for an accurate model and verification (claims, enrollment, PBM remits, rebate statements)? Options: Fully ready, Mostly ready with cleanup, Partial—significant work needed, Not ready
      • Who would need to be our day-to-day data or operations partner inside your organization, and how available are they right now?
      • What political or vendor relationships could quietly block changes even if technical and financial cases are strong?
      • On a scale from 1–10, how much change fatigue exists across your stakeholders—and where does that fatigue show up most? Options: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10

      First Small Commitments That Change the Game

      • If we proposed a low-risk proof of value, what's the smallest scope that would meaningfully convince your leadership? Options: PMPM modeling + savings estimate, Prior auth turnaround pilot, Rebate reconciliation audit, Biosimilar routing pilot, Claims accuracy validation
      • What data would you be willing to share for a pilot, and what approval or NDAs would we need to get started? Options: De-identified claims, Full adjudicated claims, Rebate statements, Enrollment files, Prior auth logs, Other
      • Who must be the named owner on your side for a pilot to proceed, and who should we copy into governance calls?
      • What timeline feels realistic for a 6–12 week pilot to surface credible signals (data handoff → analysis → validation)? Options: 4–6 weeks, 6–8 weeks, 8–12 weeks, Longer than 12 weeks
      • Which acceptance criteria would let you greenlight expansion after the pilot (select up to 3)? Options: Net PMPM reduction threshold, Improved prior auth SLA, Rebate recovery verified, Provider satisfaction improvement, Claims accuracy within tolerance, Other
      • What would make you hesitant or say no after a pilot, even if numbers look promising?
    2. Deployment Enablement

      Schedule and execute configuration, testing, provider and member communications, and claims cutover with clear owners and timelines.

    3. Validation Checklist

      Verify acceptance criteria including claims accuracy, prior auth turnaround, rebate reconciliation, and biosimilar routing before full go-live.

      Validation Questions

      Start Here: Tell Us About Your World

      • Which role best describes the person answering these questions? Options: Pharmacy Director (Health Plan), Chief Medical Officer, VP/Director of Benefits (Employer), Finance/Actuarial Lead, Other
      • How many covered lives does this pharmacy benefit manage? Options: <50,000, 50,000–250,000, 250,000–1M, 1M–5M, >5M
      • Briefly describe your benefit type and population mix (commercial, Medicare Advantage, Medicaid, ASO employer mix, clinical risk populations).
      • Which PBM functions are currently handled by your incumbent (select all that apply)? Options: Formulary design/management, Rebate contracting and reconciliation, Claims adjudication, Prior authorization administration, Specialty pharmacy management, Clinical programs (MTM, DUR), Member/provider communications, Analytics and reporting, None of the above
      • What is the single most important pharmacy outcome your leadership expects this year? Options: Reduce net PMPM, Slow specialty spend growth, Improve prior auth turnaround, Increase biosimilar adoption, Improve member access/satisfaction, Other

      Where the Money Is Slipping Through the Cracks

      • Looking at the last 12 months, what percentage of pharmacy spend do you believe is avoidable through better formulary design or rebate strategy? Options: <2%, 2–5%, 5–10%, 10–20%, >20%
      • Which three drug classes or molecules have been the biggest drivers of unexpected spend or volatility for you? Options: Oncology (injectable), Oncology (oral), Hepatitis C, Immunology/Biologics, Rare disease therapies, Specialty endocrine, CAR-T and gene therapies, Other
      • Give a concrete example of a recent contract, rebate, or formulary outcome that surprised you—and describe the impact it had on net cost or member access.
      • How confident are you in the accuracy and timeliness of rebate reconciliation from your current vendor? Options: Completely confident, Mostly confident with occasional issues, Unsure / mixed signals, Not confident
      • When reconciliation issues arise, how long do they typically take to resolve and who owns escalation?
      • How does uncertainty or opacity in rebate flows affect conversations with finance or executive leadership?

      When Processes Break: The Hidden Friction

      • How often do prior authorization or specialty access issues lead to delayed care or member/provider complaints? Options: Daily, Weekly, Monthly, Quarterly, Rarely/Never
      • What is your target prior authorization turnaround time (hours/days), and what is your measured average today?
      • Approximately what share of prior authorizations are handled automatically vs require manual clinician review? Options: >80% automated, 50–80% automated, 20–50% automated, <20% automated, Don't know
      • Describe a recent workflow or IT gap that created operational friction (e.g., claims overrides, PA portal downtime, specialty fulfillment errors). What was the downstream impact?
      • Who inside your organization is most impacted by these breakdowns (e.g., provider relations, case management, call center), and how does it feel for them when it happens?
      • What is the typical volume and type of appeals or complaints you escalate to your PBM, and how satisfied are you with their responsiveness? Options: Very satisfied, Somewhat satisfied, Neutral, Somewhat dissatisfied, Very dissatisfied

      Are Your Incentives Really Aligned?

      • If your vendor's reported savings came primarily from rebate timing and not lower net cost, would that feel like a meaningful win to your CFO? Options: Yes — savings are savings, Partially — depends on transparency, Not really — we need durable net cost reduction, Unsure
      • Which of the following best describes your current commercial model with your PBM? Options: Pass-through with fixed admin fee, Pass-through with % fee, Spread pricing, Shared savings/performance-based, Capitated/at-risk, Other
      • What level of rebate and fee transparency would you require to feel comfortable (select one)? Options: Line-item pass-through with monthly detail, Quarterly summarized reports with drill-down, Real-time dashboards with audit access, High-level reconciliations only
      • Have you had formal disputes or audit findings with your PBM in the past 24 months? If yes, what was the root cause? Options: No disputes, Rebate reconciliation discrepancies, Claims pricing errors, Contract interpretation, Data/reporting gaps, Other
      • How frequently does your executive governance team review PBM performance and financials? Options: Monthly, Quarterly, Semi-annually, Annually, Ad hoc / only when problems arise
      • How do these contracting structures make you feel about the prospect of a long-term partnership with your PBM?

      Imagine the One Number That Changes Everything

      • Which single metric, if improved by 10%, would make leadership declare the program a success? Options: Net PMPM, Specialty spend as % of total drug spend, Prior authorization turnaround time, Biosimilar adoption rate, Member out-of-pocket costs, Net drug spend variance vs budget
      • Pick up to three metrics you actively track today (select up to three). Options: Rebate yield, Net PMPM, Gross drug spend, Specialty % of spend, Prior auth TAT, Appeals/overturn rate, Biosimilar penetration, Member satisfaction (NPS)
      • For the top metric you selected, what is your current baseline and what is your stretch target over 12 months?
      • What evidence or data would you need to feel confident a proposed solution achieved the target (e.g., 6 months of validated claims, third-party audit, member outcomes)? Options: Validated claims run, Third-party reconciliation audit, Pilot with live members, Provider feedback batch, Other
      • Who in your organization must sign off on acceptance criteria (roles, not names)? Options: CFO/Finance, Chief Medical Officer, Pharmacy Director, Legal/Contracts, Employer Benefits Lead, IT/Data Security

      What Would True Operational Readiness Look Like?

      • If we asked you to run a full cutover simulation this month, how confident are you that data feeds, provider directories, and claims mapping would be ready? Options: Very confident, Mostly confident with minor gaps, Somewhat confident, Not confident
      • Which data feeds and integrations are non-negotiable for go-live (select all that apply)? Options: Real-time claims feed, Eligibility/Membership, Prescriber NPI and taxonomy, Rebate contract files, Prior auth decision feed, Specialty fulfillment feeds, Provider portals, Other
      • What percentage of historical claims would you expect us to validate pre-go-live to feel comfortable (e.g., 1%, 5%, 10%, more)? Options: <1%, 1–2%, 3–5%, 5–10%, >10%
      • Describe any security, privacy, or compliance requirements that would block data sharing or integrations unless addressed (e.g., SOC2, HIPAA BAAs, state-specific regs).
      • Who will be the operational owners on your side for cutover, testing, and post-go governance?
      • How do you prefer testing be structured: phased pilot by population, parallel run, or full cutover simulation? Options: Phased pilot by population, Parallel run with live claims, Full cutover simulation, Other

      Deciding to Change: Risks, Timing, and Commitments

      • What is the single biggest risk that would stop this change from moving forward, and why would it be fatal?
      • When is your current contract renewal window or earliest practical cutover date? Options: Within 3 months, 3–6 months, 6–12 months, >12 months, No fixed window
      • Which internal stakeholders will be most resistant to change and what are their main concerns?
      • How important is a pilot or phased approach to your decision process? Options: Critical — must pilot before committing, Helpful but not required, Neutral, Prefer direct transition
      • What contractual features or commercial protections would reduce your perceived risk (select up to three)? Options: Performance guarantees tied to KPIs, Escrows or clawbacks, Third-party reconciliation audits, Short initial term with exit clauses, Pilot with defined acceptance, Transparent pass-through accounting
      • If we proposed a 90-day proof-of-value focused on one metric you care about, which metric would you choose and why?
      • Realistically, what internal timeline would you need to make a decision after seeing pilot results? Options: Immediately after pilot, 2–4 weeks, 1–2 months, >2 months
  7. Success

    Review outcomes versus targets, surface continuous improvements, and maintain a shared channel for issues and enhancement requests.

    Success Reviews

    • Quarterly Outcomes Review
    • Monthly Operations Performance Check-in
    • Continuous Improvement Workshop
    • Issue Triage & Escalation Forum
    • Annual Strategic Review & Roadmap Planning

    Issues & Enhancements

    • Assign owners and SLAs for the top 5 tickets; update ticket statuses in the shared channel within 24 hours.
    • Ops lead to resolve or escalate top 3 incidents within agreed SLA windows and log resolution in shared channel.
    • Assign a data extract to validate any claims accuracy anomalies and report findings within 5 business days.
    • Update runbook or SOP for any recurring manual workaround agreed during the meeting.
    • Pre-work Recap & One-Sentence Current State
    • Produce 1–3 prioritized pilot experiments with clear success metrics and minimal viable scope.
    • Assign pilot owners, timelines, and data requirements to enable execution within the next 30–60 days.
    • Ensure pilots directly tie to quantified financial or clinical consequences to drive urgency.
    • Deliver pilot charters (scope, metrics, data sources, owners) for each selected pilot within 7 business days.
    • Analytics to provision required data extracts and baseline metrics prior to pilot start.
    • Communications lead to prepare a stakeholder notification plan for pilot launch and checkpoints.
    • Roll Call & Scope
    • Triage and assign priority to all open high-impact tickets and enhancement requests.
    • Ensure escalations are routed to the correct owners with timelines and communications defined.
    • Keep the shared channel current so all stakeholders have single-source visibility into issues and requests.
    • Welcome & Meeting Objectives
    • Product manager to log prioritized enhancement requests into the roadmap backlog and notify requestors of status.
    • Schedule a deep-dive meeting for any ticket requiring >3 days to resolve.
    • Year-to-Date Outcomes vs Strategic Targets
    • Approve a prioritized 12-month roadmap tied to measurable financial and clinical outcomes.
    • Confirm governance cadence, data requirements, and resource commitments to execute the roadmap.
    • Ensure roadmap choices are traced to quantified consequences to maintain executive sponsorship.
    • Finalize and publish the approved roadmap with owners, timelines, and expected ROI within 7 business days.
    • Legal/Commercial to update contract/SOW or budget amendments for any roadmap items requiring formal approval.
    • Data team to enumerate and schedule required feeds and integrations to support roadmap metrics collection.
    • Confirm whether each agreed KPI/target is met and document variances.
    • Agree validated root causes for top variances and approve corrective actions with owners and timelines.
    • Schedule concrete follow-up checkpoints and reporting cadence for action progress.
    • Owner to deliver corrective action plan with milestones and expected impact within 10 business days.
    • Analytics team to publish an updated outcomes dashboard with drilldowns for selected variances before the next check-in.
    • Schedule the next Quarterly Outcomes Review and an interim 30-day progress check.
    • Standup & Objectives
    • Clear the top operational blockers and assign ownership for SLA restorations.
    • Ensure the shared incident/enhancement channel reflects current status and next steps.
    • Identify systemic issues that require escalation to Quarterly Outcomes Review or CI Workshop.
    • KPI Snapshot
    • Consequence Mapping
    • Current-State One-Sentence Summary
    • Top Priority Ticket Reviews
    • One-Sentence Future State for Next 12 Months
    • Enhancement Request Triage
    • Outcomes vs Targets Dashboard Review
    • Prioritized Idea Generation
    • Open Incidents & SLA Exceptions
    • Enhancement Backlog Review & Prioritization Framework
    • Remediation Decisions
    • Select Pilots & Define Success Metrics
    • Escalations & Resource Allocation
    • Financial & Clinical Impact Modeling
    • Consequence & Impact Discussion
    • Pilot Planning: Scope, Owners, Timeline
    • Shared Channel & Communication Actions
    • Root-Cause Analysis for Key Variances
    • Communications & Shared Channel Updates
    • Governance, Data Access & Resourcing
    • Validation & Stakeholder Alignment
    • Roadmap Approval & Next Steps
    • Close & Next Steps
    • Decisions, Actions & Owners
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