Role Summary
As the Associate Director, Pricing & Contracting at Intellia Therapeutics, Inc., you will play a pivotal role in supporting and executing the operations of our pricing, contracting, and market access strategies as we bring our CRISPR-based therapies to market. This is a career-defining opportunity to participate in the first-ever commercialization of an in-vivo, one-time CRISPR-based therapy.
Responsibilities
- Pricing and Contracting Material Development and Workflow Management:
- Support the development of site-of-care materials related to letter of medical necessity, letter of appeals, billing and coding, ordering instructions (if specific by channel), and related office training.
- Develop trade-related materials to support pricing and distribution network information.
- Develop pricing and contracting materials to support payer account teams.
- Manage all of the above through the medical, legal and promotional review process to finalize materials.
- Develop other materials as necessary (e.g. training).
- Contract Development, Review And Tracking:
- Support business case development with National Account Directors including analytical modeling to assess the financial impact of potential offers and develop supporting offer justification.
- Communicate results of offer modeling to vet the potential offer within the Market Access team.
- Review and provide guidance and recommendations on contract language (contractual language, terms, conditions, proposals) for business applicability and patient access to support negotiations.
- Support negotiation and red-lining processes internally and externally.
- Track and report on contract lifecycle status.
- Perform lookback analysis to measure contract performance (current-state key drivers vs. original business case assumptions).
- Revenue Management Operations:
- Work with our 3rd party vendor for development of all aspects of revenue management operations pre-launch.
- Develop SOPs and policies (in partnership with external collaborators) for revenue management operations for GP methodology, Rebate and Fee Processing, FSS, Gross-to-Net.
- Support the development of these SOPs and policies as they translate to outsourced services for calculating GP.
- Maintain and update the related SOPs as business operations require.
- Work with our 3rd party vendor for management of all aspects of revenue management operations pre- and post-launch including:
- Additional system configuration (at PDUFA) for related product and related key attributes for government programs (Market Entry Date, First Sale Date, etc.).
- Government Price Reporting:
- Manage and analyze all aspects of government price reporting in compliance with Medicaid, Medicare, PHS/340B, Tricare and Federal (VA/DOD) requirements.
- Initial review of data and trends pre-calculation.
- Review and analysis of calculated government prices prior approvals.
- Support the internal approval process for government prices prior to submission to government agencies.
- Submit required quarterly AMP reports to Texas (through the VDP for TX HHS); and any other mandatory states.
- Contract set-up and related payment processing:
- Ensure contracts are set-up in 3rd party system.
- Review submitted claims data (prior to adjudication) for compliance and verification.
- Verify any off-invoice discounts (if applicable).
- Work with 3rd party vendor and internal partners through the adjudication process to generate payment packages for rebates and fees (Commercial, Medicaid, Medicare, FSS, Tricare).
- Identify and work with 3rd party vendor and any other teams to resolve discrepancies and/or claims disputes prior to finalizing prices and payment packages for approval.
- Proactively review claims and 340B transactions for diversion and/or duplicate discounts.
- Build pricing and contracting models and conduct scenario planning (rebates, WAC/ASP deltas, share shifts).
- State Price Transparency Reporting:
- Develop SOPs and policies for State Price Transparency Reporting.
- Maintain and update the related SOPs as business operations require.
- Develop manage and track State Price Transparency requirements.
- Create required submissions (as applicable per state) per quarterly and annual reporting needs, submit in advance of submission date.
- Review impacts of price on State Price Transparency reporting requirements.
- Manage state related registrations and fee payments, (including PDABs).
Qualifications
- Strong understanding of traditional and innovative contracting strategies (including outcomes- and value-based strategies as needed).
- Knowledge and experience in GP and related programs for Medicaid, Medicare, Federal Supply Schedule/Tricare and 340B/PHS (including understanding of regulations in effect and proposed regulations) and the potential impacts to our business.
- High proficiency in MS Office software (Word, Excel, Outlook, Visio, PowerPoint).
- Demonstrated experience developing analytical models to analyze contract offers and strategies.
- Excellent and confident presentation and communication skills.
- Capacity to build trusted relationships and drive strategic alignment across teams.
- Proven ability to collaborate cross-functionally and influence senior-level decision-making.
- Experience launching novel therapies with experience with medical benefit, outpatient reimbursement.
- Ability to work effectively in a fast-paced, growth-oriented environment with a commitment to addressing the unique challenges of gene editing therapies.
- Desire to learn and expand responsibilities as necessary in a fast-paced environment that is moving towards commercialization.
- Commitment to compliance, operational excellence, and continuous improvement.
- 6-8+ years in pharmaceutical or biotech industry, with a minimum of 5 years in pricing, market access, or contracting, preferably in specialty or gene therapies.
Education
- Bachelorβs degree required; advanced degree in Business, Economics, Finance, or a related field preferred.