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Intellia Therapeutics

CRISPR-Cas9 genome-editing therapeutics developer

Director Risk and Compliance Operations

Regulatory Compliance & EthicsConfirmed live in the last 24 hours
Full-timeCambridge, MA, USAIn-person

About the Job

Requirements

  • Ability to build and maintain professional relationships with internal stakeholders.
  • Demonstrated experience within Legal leading highly complex initiatives with significant risk and complexity, using cross-functional relationships and influencing skills.
  • Ability to manage multiple priorities in a fast-paced environment, adapt assignments, and work effectively with others.
  • Ability to partner with IT, Finance, Legal, and business stakeholders to drive adoption and timely delivery of system and process enhancements, including communicating with senior and executive leaders as a functional area expert.
  • Strong project and program management experience, including managing scope, timelines, risks and issues, and cross-functional stakeholders.
  • Strong analytical and problem-solving skills, attention to detail and accuracy, and ability to translate complex data and process topics into clear insights and recommendations.
  • Strong written and verbal presentation and communication skills, including creating executive-ready materials and facilitating working sessions.
  • Ability to manage sensitive and confidential matters with discretion and sound judgment.
  • Proficiency with Microsoft Office (Word, Excel, and PowerPoint), and familiarity with analytics and work management tools such as Power BI, Smartsheet, and Microsoft Project.
  • Knowledge of regulatory and compliance requirements applicable to corporate compliance, including the Anti-Kickback Statute, False Claims Act, Foreign Corrupt Practices Act, and state price transparency laws and regulations.
  • Ability to design and govern compliance systems and system-enabled processes, define controls, translate requirements into system and process configurations, and ensure sustainable operating procedures.
  • Understanding of data governance concepts and ability to establish data quality standards, definitions, and reporting requirements to support reliable analytics and decision-making.
  • Ability to quickly learn new subject areas and support emerging priorities as directed.
  • Ability to produce high-quality work with minimal oversight.
  • Bachelor’s degree in business, finance, life sciences, healthcare, or information systems (or a related field) and 12+ years of relevant life sciences industry experience, or a master’s degree or JD and 10+ years of relevant life sciences industry experience.
  • 10+ years of experience leading compliance systems and process governance, requirements definition, testing/user acceptance testing, implementation, and continuous improvement, and making decisions and recommendations regarding organizational practices, policies, and systems.
  • 10+ years of experience with data governance and operational reporting and analytics, such as dashboards, key performance indicators, and data quality.
  • Ability to sit for prolonged periods.

Responsibilities

  • Lead the operations of the company’s Enterprise Risk and Compliance Programs, ensuring that systems, processes, and reporting obligations are effectively implemented and maintained.
  • Serve as compliance lead for systems, process governance, and reporting enablement; shape scalable operational solutions, advance risk and compliance systems roadmaps, oversee enhancements and release readiness, and ensure processes are sustainable and aligned with business and regulatory expectations.
  • Lead complex cross-functional initiatives, improve data quality and process performance, and address operational and regulatory challenges.
  • Oversee and scale the internal investigations process, including case intake, evidence collection, case tracking, remediation tracking, and ongoing monitoring of corrective actions.
  • Support corporate enterprise risk management and audit programs aligned to the compliance risk assessment.
  • Own compliance tooling strategy and operations, including case management, approval workflows, third-party due diligence tools, transparency systems, learning management system interfaces as needed, and analytics.
  • Lead vendor governance and performance management for outsourced compliance services.
  • Provide leadership for data governance across compliance-owned systems and datasets by establishing quality standards, definitions, documentation, and control expectations.
  • Improve data completeness, accuracy, and usability for reporting and analytics, and partner with stakeholders to define requirements for dashboards, extracts, and other reporting outputs.
  • Build and maintain a third-party risk management program for compliance risk, including risk-based intake, due diligence, governance, onboarding, renewal, and termination processes.
  • Partner across functions to embed compliance controls into internal and vendor lifecycle activities and ensure operational design keeps pace with business needs and regulatory expectations.
  • Work across functions and organizational levels to influence decisions, align priorities, and advance initiatives.
  • Perform other related duties as assigned.

Desired Qualifications

  • Healthcare compliance program experience.
  • Experience with OneTrust and Diligent.

About the Company

Intellia Therapeutics

CRISPR-Cas9 genome-editing therapeutics developer

Intellia Therapeutics develops CRISPR-Cas9 genome editing therapies to treat severe genetic diseases. Its work centers on using CRISPR to edit genes and delivering the editing tools to the right cells with a modular lipid nanoparticle system, aiming to create treatments that can be given to patients and move through clinical trials toward market. The company earns revenue through R&D collaborations, licensing, and potential sales of approved therapies. Compared to others in biotech, Intellia emphasizes in vivo gene editing using a distinctive lipid nanoparticle delivery approach and active partnerships to advance candidates. Its goal is to bring safe, effective genome-editing treatments to patients while building value through collaborations and licensing.

Company size
501-1,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2014

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