Experience

GrandPharma (China) Co. Ltd

• Pharmaceutical Manufacturing
• 1 - 100 Employee

• 临床运营负责人

  • Jun 2020 - Present

  负责远大医药临床运营部的管理工作 负责远大医药临床运营部的管理工作



MicroPort Cardiovascular

• China
• Medical Equipment Manufacturing
• 1 - 100 Employee

• 临床运营总监

  • Dec 2019 - Jun 2020

  负责临床临床运营部的管理，包括：供应商管理、计算机系统、物资供应等 负责临床临床运营部的管理，包括：供应商管理、计算机系统、物资供应等



Medtronic

• United States
• Medical Equipment Manufacturing
• 700 & Above Employee

• Sr.Clinical Research Specialist

  • May 2016 - Dec 2019

  Project manager role: - China leader project manager for a multinational trial(81sites including 35 from China) since June2016 * CRO management (1PM and 20+ CRA) * Coordinate related stakeholders including Marketing, Sales team. * Meet study goal by working with global study manager * Budget and cost management *hold Investigator meeting Study Manager role: - Study leader for a new product regulatory study(premarket study) since Nov2017 * Design and write protocol through working with global scientists and regulatory team. Coordinator role: - Field contactor(China) for investigator initiation study0since Dec2016 * Coordinate communication between physician and global reviewer. * Manage IIS after proposal approved * Contract and payment management



IQVIA

• United States
• Hospitals and Health Care
• 700 & Above Employee

• CRA

  • Oct 2014 - May 2016

  Quintiles trainee program Monitor Quintiles trainee program Monitor



Bristol Myers Squibb

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Pharmacovigilance Associate

  • Jul 2012 - Oct 2014

  Is responsible for performing all of the required core pharmacovigilance (PV) activities including both pre-marketing and post-marketing activities for ONCOLOGY Therapy area in line with local regulatory and relevant legal requirements, and BMS procedures by directly report to the Head of Country PV. Is responsible for performing all of the required core pharmacovigilance (PV) activities including both pre-marketing and post-marketing activities for ONCOLOGY Therapy area in line with local regulatory and relevant legal requirements, and BMS procedures by directly report to the Head of Country PV.