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Director, Data Management

Maze Therapeutics · South San Francisco, CA · On-site

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About Maze Therapeutics

Backed by a16z and GV.

About the role

Join us at Maze Therapeutics as our Director of Data Management, where you will play a key role in shaping the data strategy that supports our clinical development programs. You’ll partner closely with Biostatistics, Statistical Programming, Clinical Operations, and Regulatory Affairs, and oversee external vendors to deliver high-quality, reliable clinical data across our studies.

What they're looking for

  • Bachelor’s or advanced degree in Life Sciences, Computer Science, or related field
  • 8+ years of clinical data management experience in biotech, pharmaceutical, or CRO environments
  • 3+ years of people and/or project leadership experience
  • Hands-on experience with EDC systems (e.g., Medidata Rave, Oracle InForm)
  • Strong understanding of clinical trial operations, data flows, and regulatory expectations
  • Collaborative, mentorship-oriented leadership stylewith the ability to influence across teams
More about this role

Join us at Maze Therapeutics as our Director of Data Management, where you will play a key role in shaping the data strategy that supports our clinical development programs. You’ll partner closely with Biostatistics, Statistical Programming, Clinical Operations, and Regulatory Affairs, and oversee external vendors to deliver high-quality, reliable clinical data across our studies.

Reporting to the Vice President of Biometrics, you’ll provide strategic direction and hands-on leadership for clinical data management activities spanning multiple clinical trials. Your work will ensure timely, compliant, and analysis-ready data that supports regulatory submissions and key program decisions.

  • Lead data management activities across multiple clinical studies and development phases.
  • Shape and implement data management strategies , standards, and best practices.
  • Mentor and support data management team members, fostering growth and knowledge sharing.
  • Serve as a subject matter expert for data management processes, systems, and regulatory expectations.
  • Oversee critical study deliverables including DMPs, CRFs/eCRFs, edit checks, and database locks.
  • Guide accurate, consistent, and...

Read the full posting on Maze Therapeutics's site ↗

Clinical Science

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