Management

Jubo Liu, Ph.D.  
Chief Executive Officer

  • Member of Evive Board of Directors
  • Chief China Representative of IMMTECH (AMX) where he developed its two lead products from Phase I to Phase III
  • Specialized in pharmaceutical science and support development of the first HCV drug Incivek (VX-950) during his time at Vertex Pharmaceuticals
  • Extensive experience on new drug R&D, clinical studies, regulatory and commercialization
  • PhD in Pharmaceutical Sciences, University of Toronto
 

Juhong Liu, Ph.D. 
Chief Scientific Officer

  • Responsible for company product development and regulatory filing strategy and to ensure the most efficient approach to achieve market approval
  • Previously the CMC Review Chief for Division II of Office of Biotechnology Products (OBP), managed and signatory of multiple CMC reviews of biopharmaceuticals reviewed by FDA
  • 14 years of research on molecular biology of cancer at the National Cancer Institute, published in top scientific journals such as “Cells”, “Molecular Cells”, “Nature-Structured Biology”
  • PhD in Protein Biochemistry and Molecular Biology, Peking Union Medical College

Roujian “RJ” Zhang, Ph.D.
Chief Quality Officer

  • Responsible for all aspects of Quality
  • Previously Sr. Director of Corporate Quality at AstraZeneca, Director of Quality Control at Eli Lilly and Sr. Scientist of Analytical Sciences at Amgen
  • Extensive amount of experience in quality systems, product development, international launches and lifecycle management
  • Contributed significantly to product launches, such as Cyramza® (Ramucirumab), Portrazza® (Necitumumab), Keytruda® (Pembrolizumab), Imfinzi® (Durvalumab), and Fasenra® (Benralizumab).
  • PhD in Analytical Chemistry, Purdue University

Bo Qi, M.Sc.
Senior Vice President, Chief Operating Officer China

  • Responsible for China CMC development, operations and manufacturing
  • 28+ years of experience focused on process development, characterization, validation, and commercial manufacturing operations, throughout the biologic drug lifecycle from IND to BLA and commercial launch
  • Previously Director of CMC Development, Eli Lilly; in charge of process development (PD), PD analytical and pilot plant production and directly contributed to the commercial launch of 3 oncology monoclonal antibodies
  • Prior to Eli Lilly, Director of Process Development, ImClone Systems; established the process characterization and validation platforms and contributed to the commercial launch of Erbitux
  • Directly contributed to the commercial launch of Ara-NESP (2nd generation Epogen) at Amgen
  • MSc in Biochemistry, University of Minnesota