Director, Pricing & Contracting

Posted 8 Days Ago
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Cambridge, MA, USA
In-Office
221K-270K Annually
Senior level
Biotech
The Role
The Director, Pricing & Contracting at Intellia will manage pricing strategy, contracting operations, and market access for CRISPR therapies, ensuring readiness for launch and ongoing compliance.
Summary Generated by Built In

Why Join Intellia? 

Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. 

Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done. 

We want all of our people to go beyond what is possible. We aren’t constrained by typical end rails, and we aren’t out to just “treat” people. We’re all in this for something more. We’re driven to cure and motivated for change. Just imagine the possibilities of what we can do together.   

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/ResponsibilitiesPricing 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.
RequirementsSkills/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

EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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.

Skills Required

  • 8-10+ years in pharmaceutical or biotech industry
  • Minimum of 6 years in pricing, market access, or contracting
  • Advanced degree preferred
  • Strong understanding of contracting strategies
  • High proficiency in MS Office software
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The Company
HQ: Cambridge, MA
668 Employees
Year Founded: 2014

What We Do

Intellia Therapeutics is a leading genome editing company whose mission is to develop potentially curative gene editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. We are focused on the development of proprietary therapeutics using a recently developed biological tool known as the CRISPR/Cas9 system. The promise of the CRISPR/Cas9 system is the driving force behind the creation of Intellia. Our founders have a shared belief that the CRISPR/Cas9 technology has the potential to transform medicine by permanently editing disease-associated genes in the human body with a single treatment course. This technology offers the potential for us to develop curative therapeutic options for patients with chronic diseases by addressing the underlying cause of the disease. It can bring new hope and cures to people who now have nowhere to turn for help. Our combination of deep scientific expertise and clinical development experience, along with our leading intellectual property portfolio, puts Intellia in a unique position to unlock broad therapeutic applications of the CRISPR/Cas9 technology and create a new class of therapeutic products. Intellia has the right people, assets and ambitious vision needed to take full advantage of the CRISPR/Cas9 technology’s attributes – high potency, specificity, simplicity of use, broad applicability, and multifunctional programmability – and accelerate the advancement of curative products into the clinic. View our social media community guidelines at https://www.intelliatx.com/terms-and-conditions/

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