? Contribute to clinical development strategies and develop trial outline and/or full protocol for phase 3 and phase 4 studies based on regulatory requirement and business needs to generate clinical data for new product approval and strengthen product life cycle management
? Take medical responsibility in clinical trial execution with high scientific and ethical standards to ensure the quality of clinical trial for regulatory submission and promotion use
? Generate key clinical documents and interact with Health Authority to achieve timely CTA/NDA submission and approval
? Build up relationship with KOLs/Investigators to influence them to accommodate and overcome medical or treatment procedure barriers in clinical programmes to facilitate trial execution and advocate company’s products
? Provide medical expertise in Trial Outline review within Diabetes filed to contribute to global development
? Coach medical scientists regarding the general and professional competencies, skills and knowledge in order for them to accomplish their accountabilities

是一家致力于人類健康、以先進的生物技術造福患者、醫(yī)生和社會的世界領先生物制藥公司?，F(xiàn)今在全球79個國家設有分支機構，6個國家設有生產廠，員工超過30,000人，銷售遍及180個國家。