Responsible for managing clinical trials supply in China and providing strong support to China study team, including defining clinical supplies plan of re-packaging and label design, ensure study drug and clinical devices could be delivered within agreed timeline and with good quality, managing clinical supply related budget, monitoring and handling issues raised by study team.
Responsible for management of Customs Affaires related activities and building up strong engagement and collaboration with Customs Affaires. Communicate with the Customshouse and facilitate importation and exportation, drive cross function discussion and collaboration to solve the Customs related issues. Act as Subject Matter Expert (SME) on customs policies and processes and responsible for providing instructions and trainings to AZ internal team, when necessary.
Responsible for maintaining good level of compliance with GMP, GCP, AZ SOP and related laws and r...