Clinical Trial Manager, CKD at Maze Therapeutics | CA, US | Rezi

Clinical Trial Manager, CKD at Maze Therapeutics

Clinical Trial Manager, CKD

Maze Therapeutics · CA, US

6 days ago

Clinical Trial Manager, CKD

Maze Therapeutics · CA, US

7 days ago
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About the Role

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.

Responsibilities

  • 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 materials such as CRFs, ICFs, patient diaries.
  • Act as the voice of Clinical Operations on cross-functional teams, including the Study Execution Team (SET).
  • Partner with Clinical Operations and Clinical Science Team to engage with therapeutic area KOLs and Investigators.

Requirements

  • 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.
  • Excellent verbal and written communication skills.
  • Demonstrated problem-solving and negotiation abilities.
  • Ability to work as part of a team and build strong working relationships with internal and external partners.
  • Capacity to roll-up sleeves to perform a broad range of clinical trial related tasks as needed.
  • Willingness to travel as necessary, consistent with project needs.
  • Excellent computer proficiency (Microsoft Office Suite, Project, Word, Excel, PowerPoint, Outlook).
  • Experience with clinical trial databases (e.g., Medidata Rave, Veeva, etc.).

Skills

  • Microsoft Office Suite
  • Microsoft Project
  • Microsoft Word
  • Microsoft Excel
  • Microsoft PowerPoint
  • Microsoft Outlook
  • Clinical trial databases (e.g., Medidata Rave, Veeva, etc.)

Location

  • San Francisco Bay Area

Work Type

  • Hybrid

Experience Level

  • Minimum of 4 years clinical research experience
  • 2 years as a Clinical Trial Manager

Education Level

  • Degree in a scientific discipline or health related field

Salary/Compensations

  • $143,000 - $175,000
  • Eligible for an annual performance bonus

Benefits

  • Competitive medical, dental, and vision insurance
  • Mental health offerings
  • Equity incentive plan
  • 401(k) program with employer match
  • Generous holiday and PTO policy

About the Company

  • Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing human genetics to develop precision medicines for patients with kidney and metabolic diseases.
  • Our clinical pipeline is anchored by two small molecule programs: MZE829, an APOL1 inhibitor for patients with APOL1‑mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease.
  • We are also advancing a preclinical pipeline through our Compass platform, which links human genetic variants to the biological pathways that drive disease.
  • Maze is comprised of a team of passionate and creative professionals committed to discovering and delivering transformative medicines to patients suffering from both rare and common genetic diseases.
  • 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.
  • While we have a passion for advanced science and pride ourselves on excellence in execution, ultimately, everything we do is about patients.
  • Our Core Values: Further Together, Impact Obsessed, Stand True.