Intellia Therapeutics, Inc.

Director, Pricing & Contracting

Intellia Therapeutics, Inc.$220K — $269K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required; advanced degree in Business, Economics, Finance, or related field preferred.
  • 8-10+ years in pharmaceutical or biotech industry; minimum 6 years in pricing, market access, or contracting, preferably in specialty or gene therapies.
  • Strong understanding of contracting strategies, including outcomes- and value-based.
  • High proficiency in MS Office software, particularly Excel.
  • Demonstrated experience in developing analytical models for contract offers and strategies.
  • Excellent communication and presentation skills, capable of influencing senior decision-making.

Responsibilities

  • Develop pricing and contracting materials to support payer account teams.
  • Contribute to pricing strategy using data-driven insights and competitive analysis.
  • Lead contract development, negotiation, and lifecycle management.
  • Own the relationship with third-party vendors for revenue management operations.
  • Manage all aspects of government price reporting compliance.
  • Lead development of drug compendia submissions to key databases.
  • Support state licensing processes for pharmaceutical products.

Benefits

  • Performance-based annual cash bonus.
  • New hire equity grant and eligibility for annual equity awards.
  • Comprehensive benefits package including health, dental, and vision coverage.
Full Job Description
As the Director, Pricing & Contracting at Intellia Therapeutics, Inc., you will play a pivotal role in developing 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.

This role requires an experienced and motivated individual with a strong background working with outpatient, medical benefit reimbursed drugs (e.g. specialty therapies, biologics, or cell & gene therapies). The primary purpose of the role is to own and drive pricing and contracting operations for launch readiness and post-launch activities, including: pricing and contracting strategy and material development and workflow; contract development, negotiation, review and tracking; revenue management operations; and state price transparency reporting. The ideal candidate will bring thought leadership and demonstrated experience building these processes from the ground up. Additionally, the individual should have deep experience with Government Pricing, Excel-based analytical modeling, and contracting.

This is a highly collaborative, leadership-oriented role. The individual will collaborate and coordinate with the relevant cross-functional teams including (but not limited to), Finance, HEOR, Trade and Accounts, Forecasting, Commercial Operations, and Legal. The individual must thrive in a fast-paced, build-from-scratch environment as we grow into a commercial organization in anticipation of our first launch.

The role will report to the Senior Director of Access Strategy, Pricing and Contracting, Market Access.

Duties/Responsibilities
Pricing and Contracting Material Development and Workflow Management:
  • In-line with defined strategies:
    • Develop pricing and contracting materials and training to support payer account teams
  • Contribute to and inform pricing strategy, leveraging data-driven insights, competitive landscape analysis, and pricing research.

Contract Development, Review and Tracking:
  • Evaluate and, as applicable, support the design and implementation of value-based or outcomes-based contracting strategies that align therapy value with real-world outcomes
  • Lead 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 (risk to Intellia, management within guidelines, cross-agreement implications, etc.) to support negotiations
  • Lead negotiation and red-lining processes internally and externally
  • Track, report on, and manage contract lifecycle status
  • Perform lookback analysis to measure contract performance against original base case assumptions.

Revenue Management Operations:
  • Own the relationship with our 3rd party vendor for development of all aspects of revenue management operations pre-and post launch
  • Develop and maintain SOPs and policies (in partnership with external collaborators) for revenue management operations for GP methodology, Rebate and Fee Processing, FSS, Gross-to-Net
  • Ensure accurate system configuration (at PDUFA) for related product and key attributes for government programs (Market Entry Date, First Sale Date, etc)
  • Manage and analyze all aspects of government price reporting in compliance with Medicaid, Medicare, PHS/340B, Tricare, and Federal (VA/DOD) requirements including:
    • 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
  • Oversee 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, own, and maintain SOPs and policies for State Price Transparency Reporting
  • 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)

Compendia Development & Submissions:
  • Lead the development and maintenance of drug compendia submissions to key databases (e.g., MediSpan, Red Book, Gold Standard), ensuring accurate and timely product listings to support market access and reimbursement
  • Oversee compendia data integrity across all product listings, partnering cross-functionally with Medical Affairs, Regulatory, and Commercial teams to ensure alignment with approved labeling and pricing

State Licensing:
  • Partner with supply chain to support the state licensing process to ensure the company maintains all required permits and licenses to distribute and sell pharmaceutical products across all applicable states
Coding Applications:
  • Support the development and submission of applications for appropriate billing and reimbursement codes (e.g., NDC, HCPCS, J-codes) to support product access across commercial, Medicare, and Medicaid channels.

Requirements
Skills/Abilities
  • 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

Education / Certifications
  • Bachelor's degree required; advanced degree in Business, Economics, Finance, or a related field preferred.

Experience
  • 8-10+ years in pharmaceutical or biotech industry, with a minimum of 6 years in pricing, market access, or contracting, preferably in specialty or gene therapies

#LI-KO1

#LI-Hybrid

Applications are accepted on a rolling basis, and will continue to be accepted until the position is filled at which point the position will be taken down.

The base salary for this position is expected to range between $220,554.00 - $269,566.00 USD per year.
The salary offered is determined based on a range of factors including, but not limited to, relevant education and training, overall related experience, specialized, rare or in-demand skill sets, internal comparators and other business needs. Upon joining Intellia, your salary will be reviewed periodically and additional factors such as time in role and performance will be considered. Intellia may change the published salary range based on company and market factors.

Additional compensation includes a performance-based annual cash bonus, a new hire equity grant, and eligibility to be considered for annual equity awards the value of which are determined annually at the Company's discretion.

For more information about Intellia's benefits, please click here.

About Intellia Therapeutics, Inc.

Intellia Therapeutics, Inc. is a leading genome editing company focused on developing curative therapeutics using CRISPR/Cas9 technology. The company's mission is to develop curative genome editing treatments that can positively transform the lives of patients living with severe and life-threatening diseases. Intellia's pipeline includes programs focused on genetic diseases, liver diseases, and cancer. The company was founded in 2014 and is headquartered in Cambridge, Massachusetts.
Learn more about Intellia Therapeutics, Inc.
Size
485 employees
Market Cap
$2.8 billion
Industry
Net Income
-$134.2 million
Founded
2014
5 Year Trend
+14.9%
Revenue
$57.9 million
NASDAQ

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