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Project Manager, Regulatory Affairs at Maze Therapeutics - ApplyBlast

Project Manager, Regulatory Affairs

Maze Therapeutics

3 months ago

South San Francisco, California, United States

Onsite

Full Time

Manager

1 applicant

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About this role

The Project Manager, Regulatory Affairs at Maze will support regulatory planning, timeline management, and cross‑functional coordination across development programs. The role involves maintaining integrated regulatory plans, tracking document timelines, coordinating cross‑functional teams, and ensuring visibility into priorities, progress, and risks.

Responsibilities

Maintain integrated plans and timelines for regulatory activities
Partner with Medical Writing to track document development timelines
Coordinate cross‑functional contributors across regulatory, clinical, technical, quality, and external partner teams
Track actions, owners, due dates, dependencies, open questions, decisions, and follow‑ups
Prepare agendas, meeting summaries, dashboards, and status updates

Skills

Qualifications

Bachelor's degree in scientific, health-related, or business discipline

About Maze Therapeutics

mazetx.com

Headquarters

South San Francisco, California, United States

Company Size

51-200 employees

Founded

2018

View Profile

Maze Therapeutics (branded "Genetic Navigators") is a biotechnology company that translates human genetic data into validated drug targets. They combine large-scale human genetics, computational analysis, and functional genomics to prioritize targets with strong causal evidence. Their platform is designed to accelerate and de-risk drug discovery, supporting internal development programs and collaborations with partners to advance new therapies.