Maze Therapeutics is a clinical-stage biopharmaceutical company focused on developing precision medicines for renal, cardiovascular, and metabolic diseases using human genetics. The company employs its Compass platform to identify genetic variants and link them to disease pathways, leading with two wholly owned programs, MZE829 and MZE782, targeting chronic kidney disease. Based in South San Francisco, Maze aims to deliver innovative treatments for underserved patient populations.
Open Positions
Senior Clinical Trial Manager, CKD
Bachelor’s degree in a scientific discipline or health-related field, 5-8 years of clinical operations experience, including at least 4 years as a CTM, hands-on experience managing Phases II-III clinical trials
Senior Scientist I, Computational Biology
PhD in Computational Biology or related field, 4+ years experience in computational biology or drug development, expertise in data analysis and machine learning
Scientist I, Medicinal Chemistry
Ph.D. in synthetic organic chemistry or related discipline, or M.S. with 5+ years industry experience, or B.S. with 10+ years industry experience
Senior Manager, Regulatory Affairs
5+ years of experience in regulatory affairs, Bachelor's degree required, advanced degree in life sciences
Senior Research Associate II, Medicinal Chemistry
B.S./M.S. in Chemistry, 4+ years of experience in synthetic organic or medicinal chemistry, strong organizational skills
Senior Clinical Trial Manager, PKU
5-8 years of clinical operations experience, Bachelor's degree in a scientific discipline or health-related field
Director, Clinical Sciences
Advanced degree in health sciences (PhD/MD/PharmD) with 3+ years of experience in clinical trial design, data analysis, and scientific presentations
Senior Medical Director
6+ years of drug development industry experience, MD, and experience in clinical trial design and conduct
Senior Clinical Trial Manager, Early Development
Bachelor's degree, 5-8 years of clinical operations experience, 4 years of experience as a CTM
Associate Director, Regulatory Affairs
7+ years of experience in regulatory affairs, strong understanding of ICH guidelines and US/EU regulatory requirements, hands-on experience with IND/CTAs and related submissions