Mwango Kashoki M.D., Mph

Mwango Kashoki MD MPH has a diverse work experience in the field of regulatory affairs and drug safety. Starting in 2002, they worked at the FDA as a Medical Officer, providing guidance on clinical trial design and drug development programs. They also reviewed post-marketing adverse effects of drugs. From 2006 to 2008, they served as a Clinical Team Leader/Lead Medical Officer at the FDA, reviewing Investigational New Drug applications and New Drug Applications. In 2009, they became an Associate Director for Safety, overseeing drug safety activities and serving as a senior advisor on postmarketing safety initiatives. They also authored reports and guidances related to postmarket drug safety. In 2018, they joined PAREXEL Consulting as a Vice President - Technical, and in 2020, they became the Vice President of Regulatory Affairs at Parexel Regulatory Consulting Services. They currently hold the position of SVP, Global Head of Regulatory Strategy at Parexel.

Mwango Kashoki obtained a Bachelor of Arts (B.A.) degree in Molecular Biology from Colgate University. Following that, they pursued a Master of Public Health (M.P.H.) degree from Columbia University Mailman School of Public Health. Mwango Kashoki further continued their education and earned a Doctor of Medicine (M.D.) degree from The Johns Hopkins University School of Medicine. Mwango also holds certification from the American Board of Preventive Medicine.