Timeline & Title01 Dec 2022 - 05 Sep 2024 -- Senior Clinical Data Manager I (SCDM I) -- MSD R&D (China) Co., Ltd, Beijing, China;23 September 2021 - 30 November 2022 -- Clinical Data Manager II (CDM II) -- MSD R&D (China) Co., Ltd, Beijing, ChinaProject Details1. Experienced 5 projects in different TAs including Antiviral (Global), Vaccines (Local), Oncology (Local & Global) and Infectious Disease (Local) --2023 End-year Performance Review - Outperformed --2022 GDO Role Model - Focus on what matters --High quality delivery - Pure 0 error winner in 2022 Cycle 3 --Archive 5 Milestones for IAs and Final DBL2. Support Data Validation Tool Update to solve some false output issues and to ensure completeness and accuracy of data validation, including creating/updating 30+SD, 6+report and supporting UAT testing.3. Support team perform Document Maintenance, including Newsletter review, DRP/DVP/DEG update, document archive and IR review.4. As an Integrated study BOT POC, create and maintain study RAP to reduce time spent on manual work.Special Role1. China DMC GDO Quality Team -- Perform 3 Global DVQA, 2 Individual DVQA, 1 China QA BEN QRP/QVP Quality Monitoring plan. -- As a Simulated Exam Presenter, share some quality related tips and real cases in GDO Learning Hour.2. China DMC GDO IT Team -- Create and QA VC tool for Quality BEN-- Create and maintain Power Query for External data review-- Develop a highlight tool by Macro for Embrace automation tool project-- Using Power Automate extracting data from email to excel-- Participant in 4 Cycle Theme-based Tips Sharing-- Participant GDMS Simplification Crowdsourcing-- As a Topic Share Presenter, sharing eTMF archive in Batch in GDO Learning Hour.

Accomplished validation and financial management of medical activities, followed up process and coordinated with other supporting departments