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Intellia Therapeutics

CRISPR-Cas9 genome-editing therapeutics developer

Senior Manager - Contracts

Contract ManagementConfirmed live in the last 24 hours
Full-timeCambridge, MA, USAHybrid

About the Job

Requirements

  • A bachelor's degree is required.
  • At least 7 years of experience in contract management, contract negotiation, or a related legal or commercial function; biotech, pharmaceutical, or life sciences industry experience is preferred.
  • Hands-on experience administering a Contract Lifecycle Management (CLM) system is required; experience configuring workflows, templates, or reporting is a strong plus.
  • Exceptional organizational and time-management skills, including the ability to manage a high volume of contracts and competing deadlines simultaneously.
  • Ability to work independently with minimal supervision.
  • Strong business acumen and ability to build trusted relationships with stakeholders across all levels and departments.
  • Written and verbal communication skills to explain contract terms and risks in clear, business-friendly language.
  • High attention to detail, analytical skills, and problem-solving skills.
  • Prolonged periods of sitting at a desk and working on a computer.

Responsibilities

  • Draft, review, and negotiate confidentiality agreements, master service agreements, statements of work, consulting agreements, vendor and supplier agreements, and other commercial contracts.
  • Partner with internal stakeholders across departments to understand project scopes, objectives, and risk tolerance, and translate their needs into clear, enforceable contract language.
  • Identify and flag legal, regulatory, and business risks in contract terms, and escalate issues appropriately to senior legal counsel.
  • Serve as a subject matter expert and administrator for the Ironclad Contract Lifecycle Management platform, managing templates, workflows, user permissions, reporting, and system enhancements; troubleshoot issues and support user training as needed.
  • Manage and continuously improve contracting workflows, processes, reporting, and metrics to drive efficiency, consistency, and scalability.
  • Identify opportunities for automation, process enhancement, and operational improvements across the contract lifecycle.
  • Support ad hoc legal and cross-functional projects as needed.

Desired Qualifications

  • A paralegal certificate, Juris Doctor, or relevant advanced degree is a plus but not required.
  • Experience in the biotech, pharmaceutical, or life sciences industry is preferred.
  • Experience configuring Contract Lifecycle Management workflows, templates, or reporting is a strong plus.

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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