Shuai Pan

Responsible for the global project management of Phase III clinical trials, effectively coordinating cross-departmental teams to ensure that all processes strictly comply with FDA and ICH regulations.

I am responsible for conducting on-site inspections of clinical trial sites, thoroughly verifying the authenticity, accuracy, and completeness of trial data, and ensuring that all operational procedures and data records strictly comply with GCP standards and clinical trial protocol requirements. By promptly identifying and resolving potential issues, I effectively ensure data quality and provide solid and reliable support for subsequent statistical analysis and the final submission of new drug registration dossiers.

Manage multi-center clinical trials in the field of immuno-oncology, responsible for supply chain coordination and data integrity review.