Ed Drower

Ed Drower is an experienced professional in quality assurance and clinical operations within the pharmaceutical and biotechnology sectors. Currently serving as Vice President of Quality at Suzhou Transcenta Therapeutics, Drower has established a Quality Assurance Team focused on global programs, audit management, and regulatory compliance. Drower provides advisory services for eTMF design at TMF360 and contributes to medical device processes at Cite Medical. Previous roles include Director of Quality at Xeris Pharmaceuticals, Clinical Project Director at Medline Industries, and Program Manager at Takeda Pharmaceuticals, among others. Drower holds a Master of Science in Biochemistry from Northeastern Illinois University.