Liang Li is an experienced biostatistician and managing partner with over 20 years in clinical and preclinical drug development, and more than 16 years leading statistical programs within biotech, pharma, and medical device companies. He has designed and analyzed Phase I–IV trials and registries, led statistical submissions for U.S. and international regulatory agencies, and supported FDA Advisory Committee reviews. Liang combines deep familiarity with FDA/EMEA/PMDA/ICH guidance with hands-on management of in-house and CRO-led projects, collaborating closely with medical and statistical experts to shape study design and publications. Based in Waltham, MA, he brings both technical rigor from a PhD in Pharmacology and an MS in Statistics and a pragmatic consulting mindset that helps teams navigate complex regulatory pathways. A detail-oriented strategist, he’s known for turning regulatory complexity into clear, auditable statistical plans that advance program milestones.
9 years of coding experience
6 years of employment as a software developer
The University of Utah
Bachelor of Medicine Pharmacy, Bachelor of Medicine Pharmacy at Beijing University of Chinese Medicine
PhD Pharmacology, PhD Pharmacology at University of Helsinki
Contributions:93 commits, 52 pushes, 1 branch in 1 year 5 months
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