1. Meticulous support in quality controlling and handling Individual Case Safety Reports (ICSRs) from post-marketed sources on time highlights efficiency and commitment to precision2. Successfully submitted all PBRER reports promptly within the designated timeframe and enhanced pharmacovigilance analysis per local health authority’s requirement3. Provided strong support in completing PV audit and achieving good results4. Support Health Authority interactions, including ICSR queries and Risk Management Plans (RMP) in a timely manner5. Implement and maintain the Quality Management System for pharmacovigilance according to local regulations and internal requirements 6. Manage pharmacovigilance aspects of external arrangements and partnerships (Ex. Patient Support Programs and Market Research vendors)7. Provide patient safety expertise and guidance within the local marketing company8. Actively participate in global project: ARGUS Safety Database Transition. Coordinate between regional and global project team, act as a bridge, trainer and problem solver, successfully assist regional colleagues quickly hands on new global safety database, compliance tool and QC tool.

1. Case management leader: lead case processing team. Ensure that ICSR submission. internal case processing and operation such as reconciliation with business partners and external service providers are complied with local regulation and internal requirement.2. PBRER submission to health authority3. Prepare and maintain pharmacovigilance provisions for commercial agreement: Ensure main business agreement (Ex. Distribution. out-licensing. promotion agreement…) embed appropriate PVA and conduct PVA negotiation with vendors4. Support on preparing and updating training materials and delivering trainings to partners, including internal employee’s and vendors PV training5. Responsible for Patient Oriented Program and Digital Engagement Asset: ensure programs designs follow internal safety compliance6. Monitoring literature screening activities7. Support on internal audit and achieving good results

1. Adverse reaction reporting: documentation and notification of SADR cases, SADR submission and employees’ training. Ensure that all ICSRs received from all sources are processed in a timely manner according to Excelsior’s SOP2. Product complaint handling: Contacting the manufacturer to assist with product complaint and follow-up, training & recall procedures for all employees and document submission of product recall.

1. 一般藥師（2015/09~2017/11）2. 審核藥師（2017/12~2019/04）After accumulating two years of qualifications, I was promoted to a senior pharmacist through the promotion of Chang Gung medical system.