
PhD-qualified researcher with a PharmD from Pakistan and over 9 years of experience in clinical pharmacy, hospital management, and drug regulatory control. Expertise in advanced CRISPR-Cas9 gene therapy research for Duchenne Muscular Dystrophy, including four years developing in vitro and in vivo genome editing models. Proficient in molecular biology, viral vector production, data analysis, and regulatory compliance. Seeking postdoctoral research scientist or R&D roles in biotechnology and pharmaceutical development focused on novel therapeutics for rare diseases.