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Peng Duan Location
United States
Peng Duan Work
Head of Global Regulatory Affairs and Project Lead (Maryland, US) @ (February 2023 - Present)
Director @ (January 2021 - February 2023)
Principal Consultant @ PAREXEL (April 2018 - January 2021)
Pharmacologist and Regulatory Reviewer @ (October 2012 - April 2018)
Peng Duan Education
Rutgers University 2007-2012
University at Buffalo
Ph.D (Biomedical Science)
2001-2007
China Pharmaceutical University
B.S (Pharmaceutical Analysis)
1994-1998
Peng Duan Skills
Regulatory Intelligence
Pharmaceutical Sciences
Clinical Pharmacology
Clinical Study Design
Clinical Research
Cell Culture
Cell
Molecular Biology
In Vitro
Biochemistry
ELISA
Drug Development
Immunology
Clinical Development
Drug Discovery
Cancer
Clinical Trials
Regulatory Affairs
clinical trial design
Project Management
Business Development
Clinical Strategy
Cross-functional Team Leadership
Drug Metabolism
Global Alliance Management
Global Drug Development
Leadership
PK/PD
Pharmacodynamics
Pharmacokinetics
PowerPoint
Problem Solving
Project Leadership
Regulatory Strategy Development
SPSS
Strategic Alliances
U.S. Food and Drug Administration (FDA)
global health authority engagement
Peng Duan Summary
Peng Duan, based in United States, is currently a Head of Global Regulatory Affairs and Project Lead (Maryland, US) at GeneScience Pharmaceuticals Co., Ltd.. Peng Duan brings experience from previous roles at I-Mab Biopharma, PAREXEL and FDA. Peng Duan holds a 2007 - 2012 Rutgers University. With a robust skill set that includes Regulatory Intelligence, Pharmaceutical Sciences, Clinical Pharmacology, Clinical Study Design, Clinical Research and more. Peng Duan has 2 emails and 2 mobile phone numbers on RocketReach.
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