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.
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