Dr. Ruoling Guo is the Senior Director of global clinical operations at Zhimeng Biopharma. She has built a rich and successful profile in clinical management in pharmaceutical R&D, and worked in several multi-national companies. She has managed and overseen global clinical trials in multiple therapeutic areas and at various phases of development.

Before joining Zhimeng, Ruoling was an independent consultant in the United States, providing services to companies who are seeking and conducting clinical trials in US.

Prior to moving to United States, Ruoling spent ten years in China, taking a number of positions in domestic and international pharmaceutical companies. These included global regulatory director (clinical) at Tasly, CSO at Bionorica China, and Associate Director at Sanofi and GSK. During this period, Ruoling had led multiple preclinical and clinical programs.

Ruoling obtained her PhD in medicinal chemistry from Aston University, UK. She then joined Peninsular Medical School, Exeter University in UK, as a research fellow, focusing on the efficacy and safety evaluation of herbal medicines.