Drug development, PhD, PMP, R&D, CMC, regulation
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With a PhD in life science, I have more than 10 years experience in drug development, including translational research and regulatory guidance. With a passion to improve patients' health, I continuely mastered the drug development related skills and knowledge, from science to clinical trials management, from project execution to regulation.
After abtain my PhD degree in school of medicine from NUS in 2015, I joined Cancer institute of Singapore to conduct research on translational oncology therapy. After 4 years, I joined prestige biopharma as a scientific project manager, there I was in charge of managing mAb and biosimilars development, as well as regulatory submission including IMPD, IND and MAA submission. After 3 years, I joined Hilleman Laboratories as a scientific manager where I am currently working in, to manage a conjugate vaccine and RNA vaccine.
My PhD study was in NUS. There were two major areas I studied, one is to develop a monoclonal antibody against breast cancer, one is to develop a miRNA for cancer therapy.
