Clinical and Consulting for medical device and in vitro diagnosis device (IVD)submission to CFDA, US FDA and CE.Expertized in the category of medical device and IVD for the products from clinical trial design, clinical operation, Clinical Study Report writing, investigators' meeting and response to authorities' comments. Support to the business development and bidding process, demonstrating the strength of service.

Project manager for multi-national clinical studies for hip and joint devices.

➢ Project management for writer-lead projects➢ Clinical protocol designo One phase I/IIa clinical trial of botanical drug for advanced cancer patientso Two phase II clinical trials of botanical drug for dermatology diseaseso One phase IV clinical trial of generic drug for patients after surgery of tumor removalo Review Case Report Form and Informed Consent Form➢ Clinical research strategy planningo Cell therapy for rare disease to apply US FDA INDo Medical device for in vitro diagnosis to apply US FDA and China FDAo Pediatric sedation agent to apply Taiwan FDA➢ Familiar with,o International Conference on Harmonisation (ICH) guidelineso Good Clinical Practice➢ Writing Experienceo Investigational New Drug (IND) package for US FDA submission (1 phase I/II study, 2 phase II studies) including the Investigator’s Brochure (team work)o Bridging study evaluations • Two antibody drugs for auto-immune disease• One small molecule drug for cardiovascular diseaseo Clinical study reports • A multiple site, cardiovascular disease phase III study• A pilot dermatology study• A multiple site, multi-nation oncology phase IV study • A multiple site, auto-immune disease phase IV study➢ Perform safety officer duties for clinical trialso Adverse event coding and drug codingo Annual safety report for US FDA INDo Medical monitoring for clinical safety data

• Write research proposal to National Science Council and National Taiwan University• Establish knockout mice animal model to study the mechanism the epilepsy in the lab.• Investigate the extra neurogenesis during epileptogenesis.• Investigate the anti-mossy fiber sprouting effect of lovastain after seizure.• Prepare manuscript and publish in PLoS One journal. Lovastatin modulates glycogen synthase kinase-3 phosphorylation and inhibits mossy fiber sprouting after pilocarpine-induced status epilepticus. PLoS One, 2012.

• Transfer the technology of anti-HBV herbal medicine from Industrial Technology Research Institute (ITRI) to Sunko• Establish a lab to assay the anti-HBV activity and efficacy of the herbal medicine.• Establish standard operation procedure for drug substance manufacturing.• Apply ECONBAO G for Healthy Food Certification (A00131) to Department of Healthy, Taiwan.• Conduct seminars with the distributors for the product features.

Mouse Mutagenesis Program (MMP) Core Facility, Genomics Research CenterGenerate genome-wide single point mutations of mice.Morphological and biochemical analyze the mutant phenotypes of mice.Genetic and molecular mapping of the mutant genes.Organize the mutant feature and genetic information for clients.Conduct training courses of animal care for crews and researchers.

Screen drugs that could restore pathogenic spinal muscular ataxia (SMA) transfected neuronal cell viability.Investigate the ectopic mesenchymal stem cell migration in stroke animal model.Establish embryonic stem cell in vitro differentiation model system in the lab.