two years critically assessing and reviewing new drug applications. In this capacity, I gained valuable insights into the regulatory landscape, specifically in evaluating clinical trial results encompassing efficacy and safety assessments, as well as conducting thorough risk and benefit evaluations. Additionally, I played a pivotal role in the translation of technical documents, including Informed Consent Forms (ICF), Comprehensive Study Protocols (CSP), Clinical Study Reports (CSR), and various guidelines pertinent to clinical study projects. This multifaceted experience has equipped me with a comprehensive understanding of the intricacies of drug development, regulatory compliance, and effective communication within the pharmaceutical
Full-time / Quan tâm đến làm việc từ xa
National Cheng Kung University・
Pharmacology