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The Position Step into a pivotal role where science meets strategy. 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. We thrive on diverse perspectives and bold ideas, and  we’re  looking for someone who shares that spirit.   As our Director of Medical Writing,  you’ll  lead the medical writing function and play  a central role  in the development of clinical and regulatory documents across Maze’s development programs.  You’ll  help ensure that documents are scientifically  accurate , internally consistent, fit for purpose, submission-ready, and aligned with program  objectives .   Reporting to the Vice President of Regulatory and Quality Science,  you’ll  work closely with cross-functional and external partners to advance the planning, development, and readiness of clinical and regulatory deliverables.  You’ll  also manage Regulatory Operations and Regulatory Project Management resources that support Maze’s development programs.     The Impact You’ll Have Lead the medical writing function and be accountable for the development of high-quality clinical and regulatory documents across Maze’s development programs, including protocols, clinical study reports, health authority meeting materials, and submission-supporting content.   Manage medical writing vendors and external partners to ensure  timely , high-quality deliverables that are aligned with Maze’s scientific, clinical, and regulatory expectations.   Ensure clinical and regulatory documents are internally consistent and appropriately reflect agreed program strategy, study  objectives , clinical data, and health authority expectations.   Partner closely with Regulatory Affairs, Clinical Development, Biostatistics, Clinical Operations, Safety, Quality, CMC, and external partners to support development and finalization of clinical-regulatory deliverables.   Interpret and translate clinical study source materials, including protocols, SAPs, TFLs, and safety and efficacy outputs, into clear,  accurate , and defensible regulatory documents with  appropriate cross-functional  input and alignment.   Establish and improve medical writing standards, templates, review practices, and process efficiencies to support scalable, high-quality regulatory document development.   Identify  practical opportunities to use structured content, content reuse, automation, and AI-enabled tools to improve efficiency, quality, consistency, and regulatory readiness while  maintaining   appropriate human  oversight and traceability.     As a Director, we also expect our leaders to demonstrate the following Leadership Competencies: Leadership Competencies Communication and Influence Builds communication channels across Maze for sharing information Influences Senior Management decisions through persuasive arguments Respectfully addresses differing opinions leading to support of decision Teamwork and Collaboration Champions partnerships and connections across Maze Proactively addresses issues that could result in breakdown of team relationships Spotlights team and individual contributions in public forums Execution and Results Addresses gaps and leverages strengths to get best results Maintains a steadying presence and clarifies priorities during change Anticipates and removes barriers that put functional/corporate goals at risk Develop Others and Self Removes barriers to staff development and empowers them to make