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Clinical Trial Manager, CKD

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

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About Maze Therapeutics

Backed by a16z and GV.

About the role

At Maze Therapeutics, we believe that precision medicine has the power to transform the lives of patients with both common and rare diseases. As a Clinical Trial Manager (CTM) at Maze Therapeutics, you’ll play a hands-on role in co-leading and driving the execution of our Chronic Kidney Disease (CKD) clinical trials.

What they're looking for

  • A degree in a scientific discipline or health related field
  • Minimum of 4 years clinical research experience, including 2 years as a Clinical Trial Manager at a biopharmaceutical company or CRO
  • Experience with planning and executing Phase I-II trials is preferred
  • Demonstrated proficiency in implementing, monitoring, and management of clinical trials, from start-up to close-out
  • General knowledge of FDA regulatory requirements and ICH GCP guidelines
  • Strong organizational skills, ability to prioritize and multi-task
More about this role

At Maze Therapeutics, we believe that precision medicine has the power to transform the lives of patients with both common and rare diseases. As a Clinical Trial Manager (CTM) at Maze Therapeutics, you’ll play a hands-on role in co-leading and driving the execution of our Chronic Kidney Disease (CKD) clinical trials. You’ll have the opportunity to contribute to mid to late -stage clinical studies, work cross-functionally with internal teams and external partners, and ensure trials run efficiently and with the highest quality standards. If you enjoy rolling up your sleeves, collaborating across teams, and bringing innovative medicines to patients, this role could be the perfect fit for you.

  • Steer the execution of one or more of our Phase 2 CKD clinical trials; from protocol development to achievement of corporate and study milestones such as first patient in, interim analysis, database lock, and study report completion.
  • Manage external vendors including CROs, additional key vendors, and global investigative sites.
  • Ensure adherence to study protocols, SOPs , ICH GCP guidelines by overseeing monitoring activities at investigative sites.
  • Coordinate the development of study...

Read the full posting on Maze Therapeutics's site ↗

Clinical Operations

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