Nearly 20 years of international CRO industry management and operation experience,one of the top international executives in the CRO industry,multicultural management style with experience working in the East and West

Acted as the head of dinical operations for top international CRO companies,managed annually 600-800 clinical trials,operated business in more than 55 countries/regions and lead 5,200 employees,participated in multiple cross regional acquisitions and integrations.

During her tenure at Parexel,she was directly responsible for APAC regional business management,including maintenance of big pharma and biotech customers.At FC Capital,she was also directly responsible for portfolio company's post-investment management and corresponding cinical affairs consulting

MD PhD in medicine and surgery.Five years in hospital practice.

More than 20 years working experience including 15 years in Multinational Pharma Company and CRO;Strong cross-functional leadership,local/regional/global exposure on clinical development in diversified TA areas from phase HIV,IIT studies.Possess broad local(China)regional,and global regulatory affairs expertise

During her tenure at IQVIA as a CMO,she was directly responsible for Greater China Medical team,induding 60+Medics and Regulatory experts.

More than 20 years working experience in environment ranging from start-ups to Multinational Pharma Company and CRO;Strong in drug development and multiple therapeutic indications.

Extensive international dinical trial and program management experience.Responsible for the global strategy and project direction for company pipelines, including product development from early stages to post-approval.Board expertise in building up and managing cross-functional teams.

During her tenure at IQVIA,she was directly responsible for Greater China Business Development team

Regulatory Operations and Strategy for Consultation, CTA, MAA and post marketing applications

More than 17 years experience for APAC regulatory affairs, leading total 55 staff for Regulatory Affairs in China, Korea, Malaysia,Philppines, Taiwan and Thailand and covering regulatory related consultations and submissions for APAC.

More than 13 years of global CRO experience, focusing on clinical data science.

Experience in managing a DM and Programming team of more than 90 people,serving more than 150 projedts.

Experts in data acquisition, data processing and data visualization technology solutions

More than 20 years of intemational CRO industry management and operation experience

Experienced in managing a team of over 200 project management and dinical operation sta fis in over 26 countries Worldwide and act as APAC Regional strategic consultant for over 35 key customers, more than 110 projects including pharmaceutical and Biotech companies

Clinical Operations with over 18 years experience in global CRO and pharma.

Start Up Head atop .CRO companies and managed Greater China and other Asia Pacifc countries. Combined experience fom project management clinical operation and regional start-up oversight.

Quality Management and Data Operation with over 12 years experience in global CRO and pharma, major strengths are setting up quality management systems, driving process optimization and hosting audit/inspection

Lead/Co-hnost/Support around 30 inspection and intemal/external audits over US, EU, APAC regions