Jobs at Intellia Therapeutics

Lead commercial launch of a first-in-class in vivo CRISPR therapy across OK, KS, NE. Develop territory plans, build KOL relationships, present clinical data, manage complex treatment pathways, coordinate hub and cross-functional teams, and drive access and uptake in rare disease settings.

Lead global brand strategy and US marketing for a late-stage gene editing therapy. Drive launch readiness, market development, branding, cross-functional collaboration, vendor management, budget oversight, and deliver commercial insights to support successful commercialization.

Lead strategic engagement with national and large regional commercial payers to secure coverage and reimbursement for a gene editing therapy. Build payer relationships, develop account engagement and evidence materials, inform pricing and contracting (including value-based models), partner cross-functionally on launch readiness, and influence payer policy to ensure patient access and favorable coverage outcomes.

Lead strategy, planning and execution of HCP personal promotion to support commercialization and launch of a gene editing therapy. Develop HCP materials, peer-to-peer and congress programs, manage agency partners, align cross-functionally (Medical, Market Access, Legal, Regulatory), support field training and digital rep-led engagement, and manage Promotional Review Committee processes to drive HCP engagement and product uptake.

The Director of Commercial FP&A will develop revenue models, lead financial planning for commercial operations, and establish GTN frameworks for a biotech launch.

Oversee a team applying genomic tools for gene editing therapies, managing projects, budgets, and collaborations to ensure innovative advancements.

Lead QA oversight for QC activities supporting development through commercial manufacture of gene editing products. Provide technical authority on analytical control strategies, method validation/transfers, stability programs, reference standards, investigations, trending/predictive quality, and regulatory inspection readiness. Mentor QA/QC staff and partner cross-functionally to mature QC capabilities for commercial supply.

Lead enterprise QMS strategy and digital compliance for ATMPs and biologics, drive eQMS implementation and CSV, ensure global regulatory and inspection readiness, establish data governance and analytics, manage enterprise risk, and build a high-performing quality organization across clinical to commercial stages.

Lead global transformation of QMS and digital compliance to support commercialization. Set strategic direction, govern global QMS, implement GxP standards across modalities, manage inspection readiness, drive risk-based compliance, define KPIs and analytics, ensure 21 CFR 11/Annex 11/GAMP 5 system compliance, and lead a high-performing cross-functional quality team.

The Associate Director Data Architect is responsible for managing enterprise integrations, establishing standards, driving automation, and ensuring secure, scalable connectivity across IT systems.

Manage administration, support, enhancement, and optimization of Veeva commercial and medical platforms. Act as liaison between business, IT, and vendors; translate requirements into technical solutions; lead UAT, impact assessments, process improvements, documentation, and compliance alignment (FDA/HIPAA). Provide technical leadership and oversee incident resolution and integrations.