Payer & Formulary Access
Regulated development and commercialization journeys where clinical, quality, and market access align.
Inside this journey
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Pre-Discovery
Align the room on outcomes, decision process, and constraints before deeper discovery.
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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?
- Which model best describes how you currently purchase/manage pharmacy benefits?
- 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?
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?
- 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?
- Which therapeutic areas are driving the majority of your specialty spend right now?
- How frequently do you reconcile actual manufacturer payments vs. reported rebate credits?
- 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?
- 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?
- What is your internal timeline for a vendor decision and contract execution?
- 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?
- How do providers and members usually communicate frustrations to you, and how often do these complaints reach executive leadership?
- Which parts of your prior authorization workflow create the most manual work or error-prone handoffs?
- What percentage of prior auths for specialty drugs are ultimately approved, denied, or redirected to different therapies?
- 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?
- How are rebates currently contracted (pass-through, spread, guaranteed net, hybrid)?
- How often do you receive line-level rebate detail tied to actual claims (not just lump-sum statements)?
- 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?
- Where are you on biosimilar adoption for applicable therapies and what’s blocking faster uptake?
- 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?
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?
- Which of the following KPIs must move for you to call the project a success?
- 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?
- 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?
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?
- Which data formats or standards do you currently support for integrations?
- 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?
- 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?
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?
- 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?
- 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?
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?
- What would you need from us in the next 7 days to feel this discovery was worth your time?
- 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?
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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?
- 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?
- How often do you publish formal formulary changes (e.g., quarterly, ad hoc)?
- 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?
- How do rebate flows move from manufacturer to payer in practice — direct payment, pass-through, aggregated remittance, or opaque reconciliations?
- 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?
- Which parts of the rebate lifecycle feel most opaque or risky to your finance team?
The Prior Auth Bottleneck — Who’s Really Getting Through?
- Roughly what percentage of specialty prescriptions go through prior authorization today?
- When prior auth decisions are delayed, where is the harm felt most — patient adherence, provider churn, avoidable medical spend, or something else?
- 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?
- 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?
- Which specialty fulfillment model do you primarily use?
- How often do members use out-of-network specialty pharmacies, and what are the typical drivers?
- 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?
- How are clinical equivalence and therapeutic interchange decisions made and 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?
- 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?
- Which rebate structures apply across your top 10 drugs by spend?
- How are rebate liabilities and receivables modeled into your PMPM forecasts and budgets?
- Have you experienced delays or shortfalls in expected rebate payments? If yes, describe impact and frequency.
- 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?
- Which data feeds do you currently have into your analytics environment?
- What percentage of your formulary/rebate/prior auth decisions are informed by linked member-level claims versus aggregated reports?
- 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?
Frontline Frictions: Provider and Member Voices
- How often do providers call or complain about prior authorization complexity, and what do they typically ask for?
- When members abandon prescriptions, do you have a consistent way to capture why — cost, access, confusion, or clinical reasons?
- What feedback channels exist from providers and members back into formulary or prior auth design?
- 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)?
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?
- 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)?
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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?
- Roughly how many covered lives are in scope for the program we’d be discussing?
- 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?
- 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?
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?
- What internal budget or ROI hurdle does any proposed solution need to clear to be approved?
- Which trade-offs are you willing to accept to hit financial targets (e.g., stricter utilization management, limited formulary breadth, slower prior auth turnaround)?
- 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)?
- 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?
- Which patient populations or disease areas are highest priority for improving clinical outcomes?
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?
- Which operational/experience criteria are must-haves (e.g., prior auth turnaround time, appeals rate, provider satisfaction)?
- What statistical or reporting confidence level do you need to accept a result (e.g., p-value, margin of error, rolling 3-month trend)?
- 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.
- 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?
- Which analytics or attribution methods do you trust today to tie intervention to outcome (e.g., difference-in-difference, matched cohorts, interrupted time series)?
- What level of transparency do you require on rebate flows and contract assumptions to validate net savings?
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)?
- How much internal bandwidth can you realistically dedicate to implementation and ongoing governance (FTEs, % of time)?
- 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?
- What internal approvals and legal/commercial steps must complete before we can start work?
- How will you prefer progress to be reported (format and cadence)?
- 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?
- 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?
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?
- 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?
- What additional information or artifacts can we prepare that would make your procurement and legal teams say ‘we can move forward’?
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?
- 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?
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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
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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?
- Which formulary model do you want implemented?
- What drug classes or therapeutic areas should be targeted first for redesign?
- How frequently should formulary tiering and clinical criteria be reviewed and updated?
- 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?
- What rebate contract types should be supported in scope (select all that apply)?
- What reconciliation cadence do you require for rebate remittance and reporting?
- Do you require transparent pass-through accounting and line-item visibility for each rebate?
- 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?
- What claim volumes should the adjudication flow be configured for (avg/month)?
- Are there custom benefit rules, member-level overrides, or employer carve-outs that must be implemented?
- What turnaround time SLA is required for claim processing and exceptions?
- 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?
- Which decisioning model do you prefer for prior auths?
- What PA turnaround times and SLAs are required for different categories (standard vs expedited)?
- Do you need real-time provider status updates, electronic submission (ePA), and integrations with EHRs?
- 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?
- Which fulfillment capabilities are required?
- 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?
- 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?
Operate specialty patient access and hub services
- Should vendor operate patient access/hub services (benefit investigation, PAP assistance, financial support coordination)?
- Which hub capabilities are required at launch?
- Do you need multilingual patient support or specialty nurse case management included?
- Are there manufacturer hub requirements or restrictions we must adhere to?
- 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?
Deploy step-therapy and quantity-limit utilization edits
- Which classes should have step-therapy applied initially?
- What tolerance for override/appeal volume do you expect and how should exceptions be handled?
- Do you require prospective DUR checks or real-time quantity limit enforcement at point of sale?
- Are there existing clinical guidelines or protocols to reference when building edits?
- What monitoring and rollback controls do you require for new edits (e.g., pilot cohorts, A/B test)?
- 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?
- Which biologic classes are highest priority for biosimilar adoption?
- Will you permit automatic substitution at pharmacy (interchange) or require provider notification/consent?
- Do you require metrics and reporting on biosimilar penetration and savings tracking?
- 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)?
- What standard metrics must appear on the report (select all that apply)?
- Do you require drill-down capability to member-level or provider-level details?
- What delivery format is preferred for reports (PDF dashboard, CSV export, BI dashboard)?
- Are there specific timelines or governance meetings tied to the monthly reporting cadence?
- 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?
- Which remittance cadence do you require for passing funds to the customer?
- Should vendor provide audit-ready ledgers and support third-party audits?
- Are there multi-contract scenarios needing allocation rules (e.g., multiple plans under a customer, carve-outs)?
- 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)?
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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
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Deployment
Operationalize rollout with readiness checks, enablement, and outcome validation.
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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)?
- What are the top 1–2 priorities for your pharmacy/benefits organization in the next 12 months?
- How would you describe your current relationship with your PBM(s) or vendors right now—mainly stable, fraying, or in transition?
- When you think about a successful partnership, which single outcome matters most to you personally?
- 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?
- 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)?
- How would you like success to be measured and reported (frequency and format)?
- If we achieved the financial targets but created marginally more provider work, would you consider that acceptable, or is provider burden a hard stop?
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?
- 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?
- How often do prior auth delays lead to appeals, ER visits, or provider churn in your experience?
- Which drug categories drive the majority of your volatility and why (select all that apply)?
- How does this friction feel internally—annoying, urgent, politically risky, or existential?
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?
- How often do vendor contracts or PBM practices force trade-offs you privately disagree with (e.g., clinical vs. financial priorities)?
- 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?
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)?
- 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?
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?
- How ready are your systems to deliver the data we’d need for an accurate model and verification (claims, enrollment, PBM remits, rebate statements)?
- 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?
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?
- What data would you be willing to share for a pilot, and what approval or NDAs would we need to get started?
- 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)?
- Which acceptance criteria would let you greenlight expansion after the pilot (select up to 3)?
- What would make you hesitant or say no after a pilot, even if numbers look promising?
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Deployment Enablement
Schedule and execute configuration, testing, provider and member communications, and claims cutover with clear owners and timelines.
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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?
- How many covered lives does this pharmacy benefit manage?
- 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)?
- What is the single most important pharmacy outcome your leadership expects this year?
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?
- Which three drug classes or molecules have been the biggest drivers of unexpected spend or volatility for you?
- 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?
- 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?
- 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?
- 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?
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?
- Which of the following best describes your current commercial model with your PBM?
- What level of rebate and fee transparency would you require to feel comfortable (select one)?
- Have you had formal disputes or audit findings with your PBM in the past 24 months? If yes, what was the root cause?
- How frequently does your executive governance team review PBM performance and financials?
- 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?
- Pick up to three metrics you actively track today (select up to three).
- 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)?
- Who in your organization must sign off on acceptance criteria (roles, not names)?
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?
- Which data feeds and integrations are non-negotiable for go-live (select all that apply)?
- What percentage of historical claims would you expect us to validate pre-go-live to feel comfortable (e.g., 1%, 5%, 10%, more)?
- 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?
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?
- 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?
- What contractual features or commercial protections would reduce your perceived risk (select up to three)?
- 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?
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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