Senior Manager / Associate Director, Project Management

United StatesSan DiegoExempt Full-timesenior
OtherProject Management
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Overview

Fate Therapeutics is looking for a Senior Manager or Associate Director of Project Management to join the Global Business Operations team.

Technical Tools
OtherProject Management

Fate Therapeutics is looking for a Senior Manager or Associate Director of Project Management to join the Global Business Operations team. This is a key position working closely with the Development and Technical Operations departments to manage the full lifecycle of complex projects. The role serves as a key liaison between operational execution, program development strategy, and portfolio direction across the company’s clinical stage programs. This is a full-time, exempt position and located at our corporate headquarters in San Diego, CA while reporting to the Vice President, Global Operations.

  • Manage the full lifecycle of complex CMC, clinical and product development projects.
  • Develop and maintain detailed project plans that define scope, timelines, budgets, resource allocation, and risk management strategies.
  • Translate pre-clinical, process development, analytical and clinical development program strategies into clear executable project plans and communicate them effectively across teams and senior management.  
  • Use project management tools to develop timelines, monitor progress, track key performance indicators, analyze data, and ensure accurate reporting from inception through commercial realization.
  • Lead and motivate cross-functional project teams, ensuring clear communication, collaboration, and accountability.
  • Provide regular governance updates to senior management on project status, risks, and financial performance in compliance with company FP&A policies.
  • Communicate program strategy decisions and rationale to team members and other key stakeholders to ensure alignment and informed decision making 
  • Identify, assess, and mitigate project risks and issues, developing contingency plans as needed
  • Facilitate project meetings, including kick-off meetings, core team meetings, status updates, and milestone reviews.
  • Contribute to continuous improvement of project management practices, fostering knowledge sharing and best practices across teams.
  • Ensure compliance with all relevant regulatory requirements (e.g., FDA, EMA) and internal company policies.
  • Partner with functional and executive leadership to prioritize projects and initiatives across the portfolio, balancing timelines, and resource capacity.
  • Maintain forward-looking portfolio roadmaps that integrate development programs, publications, conferences, and key external milestones.
  • Foster a culture of continuous improvement and knowledge sharing within project teams. Navigate ambiguity and support creative problem solving.
  • BS or MS degree preferably in a technical or scientific field or business administration, with 7+ years related industry/consulting experience, including management responsibilities in a cross-functional environment. 
  • A blend of CMC/clinical, operational, strategic matrix leadership experience is preferred.  
  • Knowledgeable in industry regulations and best practice in CMC and/or clinical development.  
  • Experience leading complex cross-functional and technical projects with process development, quality, regulatory, manufacturing, and clinical groups.
  • Relevant experience in pharmaceutical/biotechnology regulated manufacturing environment.
  • Demonstrated experience applying project management methodologies.
  • Proficiency in Microsoft applications and project management software (e.g., MS Project, Jira, Asana).
  • Proven track record in leading a project forward through development milestones and/or approval by mapping out deliverables and ensuring activities progress and stay on course.  
  • Knowledgeable in current and possible future trends, technology, policies, practices and information of the relevant competitive landscape and global health authority requirements for drug approval. 
  • Position is onsite at our corporate headquarters in San Diego, CA.
  • Travel may be required (up to 10%).
  • The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location.
  • Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package.
  • The anticipated salary range for this role is $155,000 - $185,000.
  • Listing Details

    Posted
    March 13, 2026
    First seen
    March 26, 2026
    Last seen
    April 25, 2026

    Posting Health

    Days active
    29
    Repost count
    0
    Trust Level
    23%
    Scored at
    April 25, 2026

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    Senior Manager / Associate Director, Project Management