Pharmacy Benefits Administration
Multi-stakeholder benefits decisions where employer groups, brokers, and members must align on coverage and cost.
Inside this journey
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Customer Discovery
Align on drug‑cost outcomes, stakeholders, constraints, and measurable success signals (trend, rebate pass‑through, network access).
Discovery Questions
Start Here: What's on Your Mind About Drug Spend?
- What's the single biggest objective you need a PBM relationship to deliver in the next 12 months?
- How would you describe your current confidence that your pharmacy vendor is delivering measurable, auditable savings?
- Which of the following outcomes matters most to your CFO right now?
- Who on your team will feel positive impact first when the PBM is performing well? Tell us their role and why.
- If you had one quick win you could point to for the next quarter, what would it be?
If This Keeps Going, What Will Break?
- What part of your drug benefit are you most worried is quietly out of control?
- How often do you see unexpected formulary disruption or therapeutic access issues when changing or optimizing PBMs?
- Give a recent example of a pharmacy-related problem that had outsized impact on your plan (cost, member complaints, or compliance). What happened and who raised the alarm?
- How long has this pain been active and what attempts have you made to fix it?
- When those issues surface, what are the usual emotional and political consequences inside your organization?
Where Are the Hidden Dollars (and Anger)?
- How confident are you that rebates reported to you reflect the full manufacturer payments tied to your members?
- Which pricing model does your incumbent PBM use today?
- Where do you suspect value is being withheld (e.g., spread on network claims, retained rebates, opaque GDUFA fees)?
- What specific reporting or auditability do you currently lack that would make rebate and net spend feel transparent to you?
- If we proposed a performance guarantee tied to net trend and rebate pass‑through, which of these would be most important to you?
Who Holds the Keys—and Who Gets Blamed?
- Who are the decision-makers and influencers for your PBM strategy, and what does success look like to each of them?
- Which stakeholder tends to be the most conservative about change—and what do they worry will go wrong?
- How do your benefits consultant and broker weigh into contracting, and have they pushed for pass-through or guarantees before?
- Who owns pharmacy clinical strategy vs. network contracting vs. rebate reconciliation in your org today?
- When problems happen, who is typically asked to explain them to leadership or regulators, and how does that affect decision-making?
Imagine a PBM That Actually Demonstrates Value
- If a PBM could prove it reduced your net drug trend by 3–5% without narrowing access, how would that change your priorities?
- What clinical or patient outcomes would you want to see tied to financial guarantees (e.g., reduced hospitalizations, improved adherence for high-cost meds)?
- Describe the ideal level of transparency you’d expect in rebate reporting and reconciliation—what would make you sleep better at night?
- What would a successful PBM transition look, sound, and feel like to your members and staff at 30, 90, and 365 days post go‑live?
- What would be an unacceptable outcome even if financial targets were met?
Data, Feeds, and the Paper Trail
- If you had to pick one data pain that would derail any optimization project, what is it?
- Which data feeds do you currently receive from your PBM and at what cadence?
- How accessible are line‑level rebate allocations and manufacturer invoices for your finance/audit team?
- When you look at your claims and network files, where do you see the biggest mapping or adjudication mismatches? Please give examples.
- What technical connectors or SFTP/API capabilities must a vendor support to be viable for you?
Switch, Small Change, or Stay Put?
- How willing are you to accept short-term disruption if it produces clear long-term net savings?
- What’s your realistic timeline for making a vendor change or for negotiating a materially different commercial model?
- What transition risks keep you up at night (e.g., claim disruption, patient interruption, financial reconciliation), and which of these would you require contractual protections for?
- Have you ever attempted to bring rebate pass‑through or guaranteed trend commitments into a contract before? What was the result and what stopped it from working?
- What minimum assurances (data access, parallel testing, financial waterfall transparency) would you need before agreeing to a go‑live date?
Commitment, Measurement, and What Success Will Look Like
- If we asked you to define three non-negotiable acceptance criteria for go‑live, what would they be?
- Which KPIs will you use to evaluate success in year one? Pick up to five.
- How frequently would you want performance reviews, and who should attend them?
- What governance structure would help you feel protected—single-point contract owner, steering committee, or external audit rights?
- Finally, what would success feel like to your members and to your CFO one year after implementation?
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Solution Experience
Model the customer’s current claims, formulary, and rebate flows to demonstrate expected financial and clinical outcomes under proposed PBM strategies.
Experience Meetings
- Modeling Kickoff & Current State Validation
- Financial Impact Modeling Workshop
- Clinical Outcomes & Utilization Modeling
- Rebate Flow, Contracting & Reconciliation Workshop
- Solution Experience Validation & Executive Decision
- Identify contract clauses that must be included to enforce the modeled pass-through and guarantees.
- Seller to update model assumptions where customer-provided corrections are validated.
- Schedule a follow-up session to reconcile any material variances (>5% PMPM) found by the customer.
- Confirm Clinical Objectives & Guardrails
- Agree on projected utilization and clinical KPI changes attributable to each intervention.
- Confirm how clinical changes are translated into financial impact and any offset assumptions.
- Define clinical acceptance criteria and guardrails to minimize member/provider disruption.
- Identify additional clinical data or stratifications needed for refined modeling.
- Customer to provide clinical stratification files (e.g., diagnosis links, specialty patient lists) if not already supplied.
- Seller to produce a clinical impact memo tying utilization changes to financial offsets and expected KPIs.
- Both parties to agree on monitoring cadence and dashboards to track clinical KPIs post-implementation.
- Review Current Rebate Waterfall
- Produce a validated rebate projection that maps to contract and reconciliation mechanics.
- Agree on reporting fields, audit cadence, and evidence required to support modeled rebate outcomes.
- Introductions & Objective Alignment
- Confirm the escalation and dispute process for any reconciliation variances.
- Customer to provide detailed rebate remittance files and any manufacturer reconciliation histories.
- Seller to draft sample contract language and reconciliation SLAs tied to modeled outcomes.
- Both parties to define a test reconciliation run to validate reporting fields and timing.
- One-Sentence Diagnosis, Consequence & Future-State Recap
- Obtain explicit executive confirmation that the modeled future state addresses the diagnosed problem.
- Secure decision to advance the validated strategy into Solution Scope or document required conditions for approval.
- List remaining risks and assign owners with timelines for resolution prior to contracting.
- Agree on delivery of final model pack and executive summary for procurement/legal review.
- Customer to provide executive sign-off or a prioritized list of conditions for sign-off within agreed SLA.
- Seller to deliver final model pack, executive summary, and recommended contract clauses to procurement counsel.
- Schedule Solution Scope workshop to translate the validated model into defined modules, deliverables, and acceptance criteria.
- Agree on one concise current-state statement that drives the modeling scope.
- Surface and quantify the key consequences that make change urgent.
- Confirm required data files, owners, and delivery dates for modeling.
- Align on a single-sentence future-state outcome the model must prove.
- Establish stakeholder roles and approval cadence for successive workshops.
- Customer to deliver anonymized claims extract (12–24 months) with defined fields by agreed date.
- Customer to provide current formulary files, rebate remittance details, and NDC-to-drug-class mapping.
- Assign data owners and confirmation contacts for each dataset.
- Seller to circulate the agreed one-sentence current-state, consequence, and future-state statements as a baseline for modeling.
- Recap Current State, Consequence & Future State
- Deliver a validated baseline financial model that matches the customer's view of current spend.
- Produce scenario outputs showing projected net cost, trend, and rebate realization for proposed strategies.
- Identify and quantify the top 3 drivers of projected savings and the assumptions that most affect outcomes.
- Obtain explicit customer confirmation on model assumptions or capture required changes.
- Agree timeline for final model deliverable and executive summary.
- Seller to deliver the model workbook with scenario tabs, driver decomposition, and sensitivity runs within agreed SLA.
- Customer to review model outputs and provide written confirmation or exception list within 5 business days.
- Proposed Pass-Through & Contract Scenarios
- Proof: Key Financial & Clinical Outcomes
- Modeling Methodology & Assumptions
- One-Sentence Current State
- Current Utilization and Clinical Risk Profile
- Intervention Mapping
- Explicit Consequence Review
- Validation: Customer Confirmation
- Baseline (Status Quo) Model Run
- Reconciliation Mechanics & Timing
- Risks, Open Issues & Mitigations
- Modeled Clinical Outcomes & Cost Tie-In
- Future State Hypothesis
- Reporting, Auditability & Controls
- Proposed Strategy Scenarios
- Contractual Clauses to Support the Model
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Solution Scope
Define included modules (formulary management, rebate pass‑through, specialty pharmacy, prior authorization, network design), responsibilities, and measurable deliverables.
Scope Configuration
- Design and Maintain Client Formularies
- Apply Real-Time Formulary Edits at POS
- Configure and Enforce Prior Authorization Rules
- Deploy Step Therapy and Clinical Edit Protocols
- Negotiate Manufacturer Rebate Agreements and Contracts
- Pass-Through Rebate Remittance and Reconciliation
- Administer Retail Pharmacy Network Contracts
- Operate Mail-Order Pharmacy Fulfillment
- Operate Specialty Pharmacy Dispensing and Management
- Run Specialty Patient Case Management Hub
- Adjudicate Pharmacy Claims and Process Payments
- Deliver Monthly Pharmacy Trend and Rebate Reports
- Administer Contractual Performance Guarantees and Credits
- Provide Real-Time Member Price Transparency Tools
Scope Questions
Design and Maintain Client Formularies
- Do you require a full initial formulary design, ongoing maintenance, or both?
- What formulary tier structure do you want us to support?
- Which therapeutic classes or specific drugs must be included, excluded, or restricted (list or attach)?
- How frequently do you expect formulary changes (updates, removals, exceptions)?
- Do you require clinical review committees or client approval gates for changes?
- Are there state Medicaid, ERISA, union, or other contract constraints we must adhere to?
Apply Real-Time Formulary Edits at POS
- Do you want edits enforced at point-of-sale, or flagged for pharmacist/provider review?
- Which edit types are required (e.g., tier override, step-through enforcement, prior-auth redirect)?
- What tolerance for override rates do you accept before requiring root-cause analysis?
- Do you need real-time messaging to members/pharmacies explaining edits at POS?
- Are there PBM switch or historical-mapping concerns for formulary codes that impact POS logic?
- Describe any specific retail POS systems or pharmacy chains requiring custom integration or testing (list):
Configure and Enforce Prior Authorization Rules
- Which drug classes or criteria should trigger prior authorization (PA)?
- Do you prefer manual PA determinations, rules-based automation, or hybrid workflows?
- What target turnaround time do you require for PA decisions?
- Should PA approvals be time-limited (e.g., 6 months) and require reauthorization?
- Do you require electronic prior authorization (ePA) integrations with prescriber EHRs?
- Are there specific clinical criteria or externally-sourced guidelines (e.g., NAS, specialty society) to embed into PA rules?
Deploy Step Therapy and Clinical Edit Protocols
- Which therapeutic areas should have step therapy protocols applied?
- Do you want hard-step enforcement (no fill until prior step tried) or soft-step (financial nudges/notifications)?
- Should step-therapy exceptions be adjudicated via clinical review, or through tiered auto-exceptions?
- What clinical or utilization data sources may be used to validate step adherence (claims history, EHR, PDMP)?
- Do you require retrospective monitoring of step therapy compliance and override reporting?
- Are there member appeals or rapid resolution timelines to incorporate into the protocol?
Negotiate Manufacturer Rebate Agreements and Contracts
- Do you require the PBM to negotiate rebates on your behalf or pass-through existing manufacturer contracts?
- Which rebate structures are acceptable (per-unit, aggregate quarterly, guaranteed minimums)?
- Are you seeking transparency into manufacturer contract terms (e.g., actual contract rates, clawbacks)?
- Do you require performance guarantees tied to rebate realization for specific therapeutic classes?
- What historical rebate performance or forecast accuracy benchmarks should be used in negotiations?
- Any anti-kickback/compliance or state-specific restrictions that affect rebate contracting?
Pass-Through Rebate Remittance and Reconciliation
- Do you require true pass-through remittance to the client or reconciliation with netting provisions?
- How frequently do you want rebate remittance and reconciliation statements delivered?
- What level of detail do you need in reconciliation (drug-level, NDC-level, manufacturer-level)?
- Do you require audit access to manufacturer contracts and PBM reconciliation methods?
- Should remittance align to client fiscal periods or to manufacturer payment schedules?
- Are there special allocation rules for rebates associated with carve-outs or carve-ins (e.g., specialty carve-out)?
Administer Retail Pharmacy Network Contracts
- Do you require an open, preferred, or narrow retail pharmacy network?
- Which retail chains or independent pharmacies are mandatory to include or exclude?
- Do you need network access guarantees (distance, percentage of members within X miles)?
- Should dispensing fees and network discounts be contracted directly or indexed to benchmarks?
- Are there pharmacy reimbursement models to support (flat fee, % of AWP/AWP-xx, usual/custom)?
- Do you require transition-of-care protections for members when pharmacies leave the network?
Operate Mail-Order Pharmacy Fulfillment
- Do you expect mail-order to be mandatory for maintenance meds or optional for members?
- What fulfillment SLA do you require for standard and specialty mail orders?
- Do you require branded packaging, adherence packaging (multi-dose), or clinical labeling services?
- Should mail-order integrate with member portals and refill reminders in real-time?
- Are there controlled-substance handling, cold-chain, or specialty shipping requirements?
- Do you require inventory reporting and forecast-driven stocking to reduce out-of-stock events?
Operate Specialty Pharmacy Dispensing and Management
- Which specialty drug classes or molecules must be supported by the specialty pharmacy?
- Do you require white-glove services (cold-chain, adherence counseling, home delivery)?
- Are you expecting clinical outcomes reporting tied to specialty management (e.g., adherence, remission rates)?
- Should specialty dispensing include hub integration for patient enrollment and manufacturer support?
- What credibility/credentialing or accreditation (URAC, ACHC) do you require for specialty operations?
- Do you require patient affordability solutions (manufacturer copay assistance, PAP facilitation)?
Run Specialty Patient Case Management Hub
- Do you want a centralized case management hub for specialty enrollment, benefits investigation, and refill coordination?
- What degree of clinical engagement is required (nurse outreach, pharmacist counseling, 24/7 support)?
- Should the hub manage manufacturer prior authorizations, patient assistance program enrollment, and appeals?
- Do you require integration between the hub and EHRs, specialty pharmacies, or manufacturer portals?
- What KPIs should the hub report (time-to-enrollment, initiation-of-therapy, abandonment rates)?
- Will the hub be authorized to act as an agent for patient financial assistance or must it only facilitate introductions?
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Mutual Commit
Finalize commercial and legal terms, performance guarantees (trend, rebate, clinical), data access, and acceptance criteria.
Agreement Modules
- Statement of Work (SOW)
- Master Services Agreement (MSA)
- Pricing Schedule & Payment Terms
- Performance Guarantees & Remediation
- Rebate Pass-Through Addendum
- Data Access & Integration Agreement
- Data Processing Agreement / BAA
- Acceptance Criteria & Go‑Live Checklist
- Pharmacy Network Transition Plan
- Formulary Transition & Clinical Protocols
- Change Order & Scope Management
- Governance & Communication Charter
- Audit Rights & Compliance Reporting
- Intellectual Property & Licensing Terms
- Termination, Transition & Data Return
- Third-Party Vendor & Subcontractor Annex
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Deployment
Operationalize rollout with readiness checks, sequencing, and validation to avoid formulary disruption.
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Pre-Deployment Readiness
Confirm data feeds, formulary mapping, pharmacy network transition plans, governance, and remediation contingencies are in place.
Readiness Questions
Quick Snapshot: Where You Stand Today
- In one sentence, how would you describe your current pharmacy benefits situation?
- How many covered lives does this PBM relationship directly impact?
- Who currently manages the PBM contract and day‑to‑day relationship inside your organization?
- When was your last major PBM change (contract switch, scope change, or implementation)?
- What reporting or analytics do you already have that we should use as our baseline?
What's Keeping Your CFO Awake?
- If prescription drug trend continues on its current path for the next 12 months, how would that change your budget or staffing plans?
- Which of the following are the biggest drivers of your pharmacy spend right now?
- How does your leadership quantify acceptable annual drug trend?
- Have budget overruns from pharmacy spend ever led to cutbacks in other programs or staffing? Tell us a specific example if yes.
- How willing is finance to accept short‑term disruption (e.g., network changes or prior‑auth shifts) in exchange for durable savings?
Are You Sure Your Rebates Reach the Bottom Line?
- How confident are you that manufacturer rebates are fully captured, allocated, and passed through to your plan?
- Who is responsible for rebate reconciliation and contract validation on your side?
- Do you receive detailed, line‑level rebate reporting (per NDC or SKU) or lump‑sum summaries?
- How often do you or a third party audit rebate remittances and contract adherence?
- If rebate transparency has felt inadequate, what was the most tangible consequence you experienced (budget gap, lost trust, negotiation failure, etc.)?
Who Really Decides When the Rubber Meets the Road?
- When a PBM change is proposed, who in your organization has final approval and why?
- Which stakeholders must be actively engaged during discovery, negotiation, and implementation?
- How aligned are clinical, finance, and procurement on priorities like rebate pass‑through, network design, and clinical controls?
- Who will act as the primary implementation/operational lead on your side and how much dedicated time can they commit?
- Are there external advisors or governing bodies (state Medicaid boards, union committees, consultants) whose approval is required? Please list and describe their role.
What Would Real Clinical Confidence Look Like?
- Would you accept giving up a portion of short‑term rebate upside if it demonstrably improved clinical outcomes and reduced total cost of care?
- Which therapeutic categories create the most clinical and financial risk for your population?
- How do you currently track clinical outcomes tied to pharmacy (adherence rates, hospital readmissions, therapy persistence)?
- What prior‑authorization or step‑therapy policies are non‑negotiable for you from a clinical perspective? Please name specific policies if possible.
- Share an example where a formulary or utilization management change improved clinical outcomes or avoided harm—what happened and how did you measure it?
How Far Are You Willing to Bend the Network to Save Money?
- If a narrower retail network reduced net trend by X%, what minimum X would justify the trade‑off in member convenience?
- Which member groups must retain broad pharmacy access for equity or regulatory reasons (rural members, Medicaid populations, specialty patients)?
- Do you have mandated pharmacy relationships we must keep (e.g., employee dispensaries, union pharmacies, state‑mandated providers)?
- What access metrics matter most to you (drive time, % within 5 miles, % in‑network pharmacies, narrow network exceptions turnaround)?
- Describe a recent member access complaint or disruption—what caused it and how disruptive was it?
If We Say 'Go', What Keeps Implementation from Turning into Chaos?
- Think back to your worst implementation experience—what single failure must we avoid at all costs?
- Which data feeds will you be able to provide for testing and go‑live (eligibility, real‑time claims, historical claims, refill history, NDC maps)?
- How clean is your formulary mapping today—do you have a mapped NDC list, therapeutic classes, and custom clinical edits?
- Which downstream partners must be coordinated during deployment (TPA, specialty pharmacy vendors, EHR vendors, enrollment platform)?
- What rollback or remediation triggers would make you want to pause or revert an implementation (claims errors, access breaches, clinical safety event)?
How Will You Know We Did What We Said?
- If we under‑perform against agreed trend or rebate guarantees in year one, what remediation would you find acceptable?
- Which of these metrics are absolute deal breakers versus negotiable?
- What baseline period and peer/comparator set should we use to measure trend and performance?
- How often do you want performance reporting and in what format (weekly dashboard, monthly executive summary, quarterly deep‑dive)?
- Who will have final sign‑off on acceptance criteria and what is your preferred dispute resolution path?
What Would Make You Confident Enough to Move Forward?
- What single commitment from a PBM would make you feel comfortable saying 'let’s proceed' today?
- What proof points would you want before committing (parallel test, retrospective audit, pilot population, escrowed guarantees)?
- How quickly would you want to see measurable impact (3 months, 6 months, 12 months)?
- Would you prefer a phased rollout (by region, by line of business, by therapeutic class) or a single go‑live?
- What internal or external obstacles could still prevent a green light after a strong commercial and clinical proposal?
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Deployment Enablement
Schedule tasks, coordinate pharmacy and vendor partners, run parallel testing, and execute member/provider communications and training.
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Validation Checklist
Verify claims adjudication, prior‑auth workflows, specialty routing, rebate reporting, and access metrics meet acceptance criteria before go‑live.
Validation Questions
Start Here: Tell Us About Your Pharmacy Benefit
- Which best describes your organization?
- Approximately how many covered lives are in scope for the pharmacy benefit we’re discussing?
- Who owns or ultimately influences PBM selection and contracting in your organization? (select all who apply)
- Who is the incumbent PBM today and when does your current contract/renewal window occur?
- From your perspective, what are the top three outcomes you need from a PBM partnership right now? (list in order)
Are You Comfortable Leaving Millions to Assumptions?
- How confident are you that the savings your current PBM reports—rebates, discounts, network fees—translate to clear dollars to your plan?
- What is your best estimate of pharmacy trend for the last 12 months (medical + pharmacy if tracked) and what drivers explain that trend?
- How are manufacturer rebates currently reconciled and reported to you? Be specific about frequency, detail, and who reviews them.
- Do you currently receive line‑level passthrough reporting (rebate by NDC, manufacturer, and contract)?
- Which financial metrics matter most when you evaluate PBM performance? (select up to 4)
What's the Human Cost Behind the Numbers?
- How often do members or providers escalate issues related to prior authorization, step therapy, or specialty access?
- Tell us about a recent case where a prior‑auth or step‑therapy workflow caused a care delay or significant member/provider dissatisfaction—what happened and what were the consequences?
- What percent of your pharmacy spend is influenced by specialty medications today, and which clinical areas are the highest risk (oncology, immunology, rare disease, etc.)?
- When members encounter a formulary denial at the point of sale, what typically follows (appeal, auto‑override, switch to alternative, member pays out‑of‑pocket)?
- How does prior authorization burden feel to your clinical team—more administrative friction, less capacity for population health work, or something else?
When the Formulary Changes, Who Gets Hurt?
- How do you react when a PBM proposes a formulary change that could remove a commonly used specialty drug—do you assume care benefit, cost savings, or member disruption will dominate?
- Which therapeutic classes are non‑negotiable for formulary restriction or step edits without clinical review?
- How do you prefer formulary changes to be governed—clinical committee review, executive approval, automatic implementation with notice, or another model?
- Describe past membership or utilization impacts when you switched PBMs—any pharmacy access gaps, mail‑order disruption, or authorization mapping issues?
- What tolerance for network narrowness are you willing to accept if it materially improves net cost (e.g., narrow specialty network to negotiate better rates)?
If Data Were a Superpower, What Would You Want to See?
- How easy is it today for you to get actionable, line‑level claims data from your PBM within 48 hours of adjudication?
- Which of these data feeds/access methods are required for you to consider a new PBM? (select all that apply)
- What KPIs or dashboards would you want available in self‑service to feel confident day‑to‑day (list top 5)?
- How do you validate PBM reports today—do you run independent analytics, rely on audits, or accept vendor reporting?
- If we could provide nightly feeds and a sandbox for forensic analysis during transition, what specific questions would you expect to be answered before go‑live?
What Would It Take for You to Risk a PBM Change?
- What level of financial performance guarantee would make you comfortable switching PBMs—would you need guarantees on trend, rebate pass‑through, clinical outcomes, or a combination?
- Have you ever enforced a PBM performance guarantee? If yes, what failed or succeeded in that experience?
- How important is contract flexibility for you—ability to change formulary, amend network terms, or accelerate audits mid‑contract?
- What financial or operational thresholds would trigger a remediation or termination right (e.g., >X% trend variance, rebate shortfall >$Y)?
- Would you consider shared‑savings or outcome‑based models where vendor upside/downside is tied to total cost or clinical measures?
Deployment Anxiety: What's Most Likely to Break?
- When you think about a PBM transition go‑live, what single operational failure worries you most (claims errors, lost prior‑auth rules, specialty fulfillment gaps, rebate misattribution, or other)?
- Do you have an internal playbook or preferred runbook for vendor transitions (data mapping, parallel testing, rollback criteria)?
- What acceptance criteria must be met in parallel testing before you sign off on go‑live (examples: <0.5% claim variance, 100% NDC mapping, PA throughput time, etc.)?
- Which parties must be coordinated during deployment (select all that apply)?
- What cadence and format of status reporting during deployment would make your team comfortable (daily ops calls, weekly executive summaries, real‑time dashboard)?
What Would Success Feel Like — A Year from Now
- Imagine it’s 12 months post‑implementation: what three measurable outcomes would make you call this a success?
- How would improved rebate pass‑through or lower net trend change conversations with your CFO or board—more flexibility, headcount, or investment elsewhere?
- What ongoing governance rhythm would you prefer to track results (monthly ops, quarterly business review, annual contract refresh)?
- If outcomes fell short of the agreed targets, what remediation would feel proportionate—financial credits, operational remediation plan, or contract termination?
- Are there any non‑negotiable constraints we should know up front (state procurement rules, union contracts, existing vendor clauses, data privacy requirements)?
Signals to Move Forward — Quick Checks
- How soon do you realistically need a PBM solution in place to affect your next renewal?
- Who needs to be included in the next meeting to make progress (name roles or teams)?
- Which of these would be most persuasive as a next step: an independent financial model, a technical readiness checklist, a clinical operations demo, or a pilot program?
- What would be the single most important deliverable from a Discovery phase to help you decide to proceed?
- Are there any red lines or deal terms you will not accept that we should know now (e.g., no spread pricing, full pass‑through, specific indemnities)?
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Success
Review outcomes against agreed success metrics, reconcile rebate performance, and maintain a shared channel for issues and continuous improvement.
Success Reviews
- Quarterly Success Review
- Rebate Reconciliation & Transparency Workshop
- Clinical Outcomes & Utilization Validation
- Continuous Improvement Governance & Shared Channel Setup
- Rapid Issue Triage & Remediation Simulation
Issues & Enhancements
- Prioritize the initial continuous improvement backlog and assign owners for first experiments.
- Define an auditable reconciliation process and scheduled cadence for future periods.
- Publish final reconciliation statement with supporting extract files and calculation workbook within 5 business days.
- Initiate agreed invoice/credit adjustments and confirm accounting entries with finance teams.
- Implement automated reconciliation report and threshold alerts to the shared channel for next period.
- Current Clinical State (One Sentence)
- Validate whether clinical KPIs and acceptance criteria have been met and document any breaches.
- Identify clinical root causes and approve targeted interventions to improve member outcomes.
- Assign owners for clinical remediation and set measurement checkpoints.
- Produce drill‑down reports for top 5 therapeutic drivers of variance and circulate within 3 business days.
- Implement approved clinical rule adjustments in a controlled test environment and report results at the next checkpoint.
- Notify impacted provider groups and members per agreed communications plan if access or routing changes are enacted.
- One‑Sentence Future State
- Approve governance model and cadences that balance speed of resolution with executive oversight.
- Stand up a shared, auditable communication channel and reporting templates for all stakeholders.
- Opening & Objectives
- Create the shared channel, set access controls, and post onboarding instructions within 2 business days.
- Publish the RACI, cadence calendar, and SLA document to the channel and share with all stakeholders.
- Populate the initial improvement backlog with owners, hypotheses, and success metrics.
- Incident Learning Snapshot
- Confirm triage workflows function in practice and that roles/SLAs are realistic.
- Identify procedural gaps and immediate fixes to reduce time‑to‑resolution for future incidents.
- Ensure staff are trained and confident in using the shared channel and escalation paths.
- Produce a finalized triage SOP and incident playbooks for the top 5 incident types and publish to the shared channel.
- Schedule hands‑on training for operational teams on the shared channel and triage process within 10 business days.
- Implement monitoring alerts for the top 3 incident signals and connect them to the shared channel for automatic triage initiation.
- Ensure shared, unambiguous understanding of current performance against contract KPIs.
- Identify root causes for any shortfalls and agree on concrete remediation with owners and timelines.
- Authorize any financial adjustments or credits and schedule validation checkpoints.
- Deliver a reconciled metric pack (trend, utilization, rebate pass‑through) with source extracts and calculation workbook within 7 business days.
- Assign owners and deadlines for each remediation item; publish a remediation tracker to the shared channel.
- Schedule the next success checkpoint and any interim technical deep dives required for disputed items.
- Pre‑read Confirmation
- Reach mutual agreement on rebate amounts and how pass‑through was calculated for the period.
- Document open disputes, evidence needed, and timelines to resolution.
- One‑Sentence Reconciliation Current State
- Consequence Framing
- One‑Sentence Current State
- Governance & RACI
- Triage Workflow Walkthrough
- Shared Channel Design (Proof)
- Consequence Summary
- Dashboard Walkthrough (Proof)
- Walkthrough of Rebate Calculations (Proof)
- Simulation Scenarios (Execution)
- Metrics Deep Dive (Diagnosis)
- Program Effectiveness & Exceptions (Diagnosis)
- Variance & Dispute Triage (Diagnosis)
- Issue SLA & Escalation Workflow
- Post‑Incident Reconciliation & Learning
- Improvement Backlog & Experimentation Process
- Calibration & Next Steps
- Acceptance Criteria Validation (Decision)
- Settlement & Documentation (Decision)
- Root Cause & Variance Analysis (Proof)
- Cadence & Automations
- Clinical Improvement Plan
- Onboarding & Access Steps
- Decision & Remediation Planning (Validation)
- Next Steps & Follow‑Up Cadence