Maze Therapeutics

Regulatory Project Manager/Senior Manager

South San Francisco, CA · Senior

Sponsorship not specifiedDetected 19 hours ago
Project ManagementFDA RegulatoryAnimal StudiesCommunicationCollaborationRegulatory Affairs

About the role

  • This is an opportunity to help bring structure, visibility, and execution discipline to a growing Regulatory function at Maze.
  • At Maze, we're on a mission to uncover genetic insights and transform them into precision medicines that change lives.
  • Our team is driven by curiosity, collaboration, and a commitment to improving treatment for people with severe diseases.

Responsibilities

  • Coordinate cross-functional contributors across regulatory, clinical, technical, quality, and external partner teams to keep regulatory workstreams moving.
  • Help establish fit-for-purpose project management tools, trackers, templates, and working practices that create structure without adding unnecessary process burden.

Requirements

  • 5+ years of project management experience in the biopharmaceutical industry, with experience supporting Regulatory Affairs, clinical development, or regulatory submission activities.
  • Strong organizational judgment and attention to detail, with the ability to track actions, dependencies, decisions, risks, and follow-ups across multiple workstreams.

Nice to have

  • advanced degree or project management certification preferred.
  • proficiency with common project management tools preferred.

Compensation

  • Maintain integrated plans and timelines for regulatory activities, including health authority interactions, IND amendments, annual reports, major program milestones, and future submission activities.

Benefits

  • Maintain integrated plans and timelines for regulatory activities, including health authority interactions, IND amendments, annual reports, major program milestones, and future submission activities.
  • Partner with Medical Writing to track document development timelines, review cycles, comment resolution, approvals, and readiness dates for key clinical and regulatory documents.
  • You'll help ensure that regulatory activities, health authority interactions, medical writing timelines, and submission-related workstreams are organized and moving forward with appropriate accountability.

Company info

  • MZE829, an APOL1 inhibitor for patients with APOL1‑mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease.
  • We are also advancing a preclinical pipeline through our Compass platform, which links human genetic variants to the biological pat
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