Background
Focus Areas
Professional regulatory affairs consultant and project manager with a proven track record of success
Regulatory filings to the US FDA including PIND/IND
FDA meetings
ODD and expedited programs
Early-stage drug development and project management
Bill Zhao is the Regulatory Affairs Manager at Eliquent Life Science. Specializing in regulatory affairs-related project management, Bill collaborates with cross-disciplinary teams and sponsors to address regulatory challenges and achieve significant milestones.
Bill Zhao is a result-driven professional with a versatile skill set in regulatory affairs and project management. He excels in fast-paced, timeline-driven environments, demonstrating strong abilities in project planning, multi-disciplinary collaboration, and timeline management. With an in-depth understanding of drug and biologic development regulations, Bill has extensive experience in Investigational New Drug (IND) filings, eCTD publishing, and ESG submissions. His project management expertise includes strategy implementation and cross-functional coordination, showcasing accountability and flexibility. Fluent in English and Chinese, Bill is proficient in communicating across diverse cultures and functions.
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EDUCATION:
Master of Science in Healthcare Decision Analysis, University of Southern California
Bachelor of Science in Statistics, Shanghai University of Finance and EconomicsCERTIFICATIONS:
The Regulatory Affair Certification, 2023 -
PROFESSIONAL EXPERIENCE:
Senior Regulatory Project Manager at Eliquent Life Science, Inc. (Legacy “DataRevive USA LLC”)
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