Dr. Shuaizhi Du

• Conducting pioneering research on glucocorticoid-catecholamine synergies to address lung inflammation and peritonitis. • Executing GLP-compliant animal handling and immunology models, building foundations for clinical trial development and drug R&D. • Optimizing ChIP-seq and multi-color flow cytometryprotocols to enhance glucocorticoid receptor integrity and resolution pathways.

• Finalized/defended PhD in biomedical sciences while upskilling in data science and bosting R/tidyverse for multi-omics/clinical analysis. • Completed Project Management training, preparing for clinical trial coordination and GCP-compliant project leadership.

1. Conducted in-depth data analysis, publishing a manuscript in "Endocrinology" on steroid hormone-induced responses in oviduct epithelial cells. 2. Contributed to the setup of a cell lab, refining SOPs for 3D cell culture and molecular assays, ensuring regulatory compliance. 3. Co-trained junior students in molecular techniques (e.g., RT-qPCR( and collaborated on immunoassay development for sex steroid detection in diverse materials, emphasizing SOP adherence, data integrity, and metabolic evaluation.

1. Research topic (Fertility impairment by maternal stress: impact of cortisol on oviduct epithelium functions). 2. Proficiently isolated, cultured, and characterized primary oviduct epithelial cells, and replicated the oviduct epithelium preserving in vivo physiological properties. 3. Conducted molecular and immune assays (e.g., RT-qPCR and ELISA), and examined the morphological, bioelectrical, transcriptomic, and proteomics response of cells to hormonal (cortisol, estradiol, and progesterone) exposure.

1. Led collaborative veterinary vaccine projects, ensuring scientific integrity and regulatory compliance. 2. Directed a 4-member team, specializing in the pre-clinical vaccine studies, with a focus on SOPs and GLP compliance. 3. Contributed to research plan design, overseeing experimental vaccine manufacturing in cell bioreactors for pre-clinical testing. 4. Reviewed study reports, maintained data documentation, adhered to GLPs, and contributed to GMPs compliance, QA testing, and regulatory affairs.