Maze Therapeutics

Clinical Trial Manager, CKD

South San Francisco, CA · Mid

Sponsorship not specified$143k-$175kDetected 64 days ago
GCPNegotiationExcelClinical TrialsClinical ResearchFDA RegulatoryResearchAnimal StudiesCommunicationProblem SolvingOrganizational SkillsMicrosoft Office

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.
  • 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.

Responsibilities

  • Manage external vendors including CROs, additional key vendors, and global investigative sites.
  • Partner with Clinical Operations and Clinical Science Team to engage with therapeutic area KOLs and Investigators.
  • We are also advancing a preclinical pipeline through our Compass platform, which links human genetic variants to the biological pathways that drive disease.
  • Maze performs position-based compensation benchmarking to industry market data to ensure we pay competitive wages.

Requirements

  • Minimum of 4 years clinical research experience, including 2 years as a Clinical Trial Manager at a biopharmaceutical company or CRO.
  • 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.
  • Excellent computer proficiency (Microsoft Office Suite, Project, Word, Excel, PowerPoint, Outlook).
  • Experience with clinical trial databases (e.g., Medidata Rave, Veeva, etc.).

Nice to have

  • Experience with planning and executing Phase I-II trials is preferred.

Skills

  • Ensure adherence to study protocols, SOPs, ICH GCP guidelines by overseeing monitoring activities at investigative sites.
  • Coordinate the development of study materials such as CRFs, ICFs, patient diaries.

Compensation

  • The expected annual salary range for employees located in the San Francisco Bay Area is $143,000 - $175,000.
  • The expected salary range for this role may be modified in the future.

Benefits

  • We are fostering a culture that encourages vision, initiative and the development of talent.
  • Our supportive work environment inspires creative thinking and freedom of expression, resulting in a stimulating atmosphere where people enjoy coming to work.
  • Additionally, this position is eligible for an annual performance bonus.

Company info

  • Further Together - Our path is paved with challenges, but with resilience and a team-first mentality, we'll achieve our mission.

This listing is sourced directly from Maze Therapeutics's careers page and normalized into a canonical job model.