About > Management Team
  • Li Chen, PhD

    Founder and CEO

    Dr. Li Chen, Founder, Executive Director, Chief Executive Officer, and Chief Scientific Officer. leads Hua Medicine a clinical stage biotech company whose mission is to bring personalized diabetes medicines to patients in China and worldwide. He is a pioneer in collaborative innovation in China and advanced Hua Medicine with an operation principle of high standards, high quality and create high value. Hua Medicine leverages global resources to develop GKA and completed 6 clinical studies in China and USA, in which the HMS5552, a novel GK PAM demonstrated desirable safety and efficacy profiles together with an improvement of beta cell function in Chinese T2DM patients. Under his leadership, Hua Medicine completed successfully a POC study and initiated China NDA enabling process. During this period, Hua Medicine raised 200M USD and established the leading position of Hua Medicine in China biotech industry.

    Li received his PhD at Iowa State University and joined Roche R&D center in USA in 1992. With 18 years at Roche, Li advanced his career from a medicinal chemist to the head of High Throughput Technology, and later CSO of Roche China R&D Center with a membership at Roche Research Leadership Team. He is an inventor of 35 granted patents and an author with over 60 publications.

  • George Lin, J.D.

    EVP & Chief Financial Officer

    Mr. George Lin, J.D., a healthcare veteran brings with him over 20 years of investment banking and legal experience working with numerous private and public companies globally.  Prior to joining Hua Medicine, he was Asia Pacific Head of Consumer, Retail and Healthcare Investment Banking and Head of Hong Kong and Taiwan Investment Banking for Bank of America Merrill Lynch based in Hong Kong.  As an investment banker and corporate lawyer focused on healthcare, retail and the consumer sectors, Mr. Lin was previously based in Los Angeles and San Francisco before moving to Hong Kong in 2007.  His experience entails IPOs, debt and equity financings and M&As for leading companies in Asia, the United States and Europe.  In the last 10 years alone, Mr. Lin has led M&A transactions valued (in aggregate) in excess of US$20 billion and raised financings valued (in aggregate) at over US$40 billion.  Since April 2018, Mr. Lin has served as a member of the Biotech Advisory Panel of the Hong Kong Stock Exchange.   Prior to Bank of America Merrill Lynch, Mr. Lin also worked at Credit Suisse as an investment banker in their Hong Kong, San Francisco and Los Angeles offices, and at O'Melveny & Myers LLP as a corporate attorney in their Los Angeles Office.  Mr. Lin received a Bachelor of Sciences degree in Biological Sciences from the University of California at Davis and a Juris Doctor degree from The University of Chicago Law School.
  • Daniel Du, PhD, M.D.

    SVP, Regulatory, Medical Safety and Manufacture

    Dr. Daniel Du has worked in pharmaceutical industry for more than 20 years with broad experience in drug discovery, clinical development and regulatory submission. He was instrumental in discovery of multiple clinical candidates and played significant roles in multiple IND and NDA submissions when he was working in two of the fortune 500 pharmaceutical companies. He is also a skilled clinician and medical monitor for clinical studies, experienced in safety management, and authored the clinical sections for multiple NDA filings. He is the inventor of over 15 patents and authored over 20 manuscripts. Dr. Daniel Du received Medical degree from Beijing Medical University and PhD of Pharmacology and Toxicology from Albany Medical College, NY. He received US Education Certificates for Foreign Medical Graduates (ECFMG).

  • Yi Zhang, PhD, M.D.

    SVP, Clinical R&D

    Dr. Yi Zhang heads the clinical research & development team at Hua Medicine, and currently as the senior vice president since April 2018. Prior to joining Hua, Dr. Zhang was the Associate Medical Director of Clinical Science at Roche Product Development group, Asia Pacific region. She served as a clinical scientist for innovative drug development in the areas of cardiovascular, metabolic and renal diseases. Prior to Roche, Dr. Zhang was a Physician and an Associate Professor at Shanghai Ruijin Hospital, Shanghai Jiaotong University School of Medicine with more than 10 years' clinical experience. Dr. Zhang was also a team leader of the molecular genetics research group at the Shanghai Institute of Hypertension and a principle investigator for several projects supported by the National Natural Science Foundation of China and the Shanghai Municipal Natural Science Foundation. Dr. Zhang obtained her Doctor of Medicine and PhD degrees from Shanghai Jiaotong University School of Medicine(specialization in cardiology)  She received training in molecular genetics, bioinformatics and epidemiology at the Chinese National Human Genome Center and at the Framingham Heart Study as a NIH/NHLBI visiting researcher. Dr. Zhang has received Shanghai Subject Chief Scientist and 60 publications in journals such as Nat Genet, Circ Cardiovasc Genet, Hum Mol Genet, 4 book chapters, and has 3 China patents.

  • Jin She, PhD

    VP, Chemistry

    Dr. Jin She is responsible for API manufacturing, Process Chemistry Research & Development, and Discovery Chemistry at Hua. Dr. She has over 11 years’ experience in the biotechnology and pharmaceutical industry. Prior to joining Hua Medicine, he worked at MSD R&D Center (China) as Director of Process Chemistry, and Roche R&D Center (China) as Head of Process Research &Synthesis. Before returning back to China from the US, he worked at Inspire Pharmaceuticals Inc. as Sr. Research Scientist and team leader of Process Research. Dr. She has also been an Industrial Advisor for Engineering Master Program at East China Science & Technology University for the last 5 years.He has 8 publications in peer-reviewed journals and 6 patents. Dr. She Received his PhD in organic chemistry from the University of North Carolina at Chapel Hill. He obtained his BS and MS degrees in chemistry from Beijing University.
  • Fuxing Tang, PhD

    VP, CTO

    Dr. Fuxing Tang obtained his Ph.D. in Pharmaceutical Sciences from the University of Florida. In addition, Dr. Tang conducted postdoctoral research in peptide delivery in Professor Ronald Borchardt’s group, which is well known for their work in Caco-2 cells. Before joining Hua Medicine, Dr. Tang worked in the pharmaceutical industry and regulatory affairs for 20 years. Dr. Tang worked as reviewer in the Office of Regulatory Science of the U.S. Food and Drug Administration, and worked in TEVA and Allergan as Global Director of Biopharmaceutical Sciences. Dr. Tang started his career at Forest labs, Inc. During his tenure at Forest labs, Inc/Allergan, Dr. Tang was instrumental in building various biopharmaceutical functions and in charge of multi-functions of ADME, preformulation, drug product process optimization and product post-approval manufacture process optimization.
    Dr. Tang and his team made significant contributions in multiple successful IND/NDA filings and supported post-approval manufacturing for drug products such as Lexapro®, Namenda®, Namzaric®, Linezess®, Vraylar®, Viberzi®, among others, of which Lexapro®, Namenda® are blockbuster products with peak annual sales of US$2 billion. At Allergan/TEVA, Dr. Tang and his team supported drug development for both NDA and ANDA. Dr. Tang and his team significantly contributed to multiple first-to-files ANDA approvals such as doxycycline and abuse-deterrent-formulation (ADF) morphine sulfate.
    Dr. Tang authored/coauthored more than 20 peer-reviewed research articles/patents across various fields, including organic synthesis, gene delivery, pre-formulation, formulation, and ADME studies.
  • Yilei Fu, MBA

    VP, Quality Assurance

    A seasoned leader in quality control and assurance with over 20 years experiences in the Pharma industry across sites and countries at AstraZeneca, Xian Janssen and Boehringer-Ingelheim (Germany & China). In his extensive knowledge and experience with proven track records for hosting various regulatory GMP, GSP inspection successfully include EU, TGA and CFDA authorities. Also Mr. Fu have rich hands-on experience for leading company Quality Culture change, continuous improvement of quality management systems and building high performing quality team. He is taking overall quality management responsibilities for Hua’s QMS systems and as executive co-chairman for Quality & Safety committee. Mr.  Fu is licensed pharmacist and owns master degree of business administration from Shanghai Jiaotong University.

  • Wenjie Xu

    VP, Commercial Strategy and Marketing

    Wenjie Xu, serves as vice president, Head of Commercial Strategy and Marketing. Prior to joining our Group, Ms. Xu served as Executive Director of the Cardiovascular, Renal, and Metabolic Business Unit of AstraZeneca China from January 2016 to August 2018. Ms. Xu's principal responsibility at AstraZeneca China was sales and marketing of their diabetes franchise in China, including the successful launch of Dapagliflozin. Prior to AstraZeneca, she also served in various sales and marketing roles at Eli Lilly from February 2007 to December 2015, focused on diabetes starting in 2009. Prior to Eli Lilly, Ms. Xu served in sales and marketing functions of various pharmaceutical companies, including Amgen China. Ms. Xu obtained her bachelor’s degree in pharmaceutical analysis from the China Pharmaceutical University in 1993, and a master of business administration degree from Goizueta Business School, Emory University, in 2004.
  • Shuang Ren, PhD

    Senior Director, Clinical Pharmacology

    Dr. Shuang Ren is responsible for Bioanalytical, Preclinical Pharmacology, and Clinical Pharmacology at Hua Medicine. Dr. Ren has over 11 years’ experience in drug research and development at various top 10 international pharmaceutical companies as clinical pharmacologist and DMPK project leader in different disease areas (metabolic diseases, respiratory disease, oncology, CNS and infectious disease). Prior to Hua Medicine, she worked at the Novartis Institutes for Biomedical Research (NIBR) Shanghai Center as Investigator in Clinical Pharmacology, and Roche R&D Center (China) as Senior Scientist in DMPK. Dr. Ren received her PhD in molecular biology and biochemistry from Tong Ji University. 

  • Haoliang Song, PhD

    Senior Director, Preclinical Drug Safety

    Dr. Haoliang Song is Director, Drug Safety Assessment at Hua Medicine. Now he is managing all the drug safety-related studies, cooperating with the partners from US, China and other countries. As a member of Hua Medicine QQLT, Dr. Song also attends the Quality control strategic development of Hua Medicine projects. Dr. Song has more than 16 years experience in hospital and biotechnology company. Before joining the company, Dr. Song worked at Medicilon as Director of Operations and Study Director to lead teams in the development of GLP and non-GLP preclinical studies. He received USFDA GLP regulation and study trainings including study design and study operations & management at US MPI RESEARCH. Prior to that, Dr. Song spent several years at Hong Kong Polytechnic University as Research associate and its institute of Modern Chinese Medicine as Head of Pharmacology department, leading teams in the development of pharmacology and toxicology techniques platform, where he completed the studies for the doctoral thesis. Dr. Song also had five years working experience in hospital, where he had more close attention on how to meet the patients’ needs. Dr. Song is the author of more than 10 publications and one of the inventors of 4 patents.

  • Michelle Zhu

    Senior Director, Industrial Policy & Regulation

    Michelle is a seasoned leader in China pharmaceutical policy and regulation over 20 years in China with rich experience in market access and government policies. Prior to joining Hua Medicine, she has worked with Boehringer-Ingelheim, Abbott and J&J China operation and established her leadership in the drug price negotiation, market entry and establishment of joined ventures. She was in charge of market access affairs and responsible for developing government affairs strategies to achieve company’s business goal. Michelle has also managed government relation operation, which focused on reimbursement and pricing. She cooperated with government agencies/organizations and Industry Associations for monitoring central and provincial government policy changes.


  • Gary Yu

    Senior Director, Regulatory Affairs

    Gary Yu,Master of pharmaceutics, senior engineer. Now he serves as Director of Regulatory Affairs in Division of Clinical Research and Development. Prior to join Hua, Gary was in charge of two developing projects of innovative T2DM drug candidates and managed a series of tasks that preclinical evaluation, clinical development and regulatory affairs are included. One of these projects was supported by National Key Technologies R&D Program and has been accomplished in 2013. Gary has more than 10 years’ experience of Medical R&D project management and Pharmaceutical license progress. Gary has also participated as inventor in writing and registration of several domestic and PCT patents.

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