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A results-driven pharmaceutical research and global health professional with extensive experience in pharmaceutical and global health organizations. Skilled in directing global health programs to develop pharmaceutical policies, strengthen health systems, and advocate for increased access to affordable, quality-assured medicines.
I am a highly motivated regulatory affairs professional with over 10 years of experience in the pharmaceutical industry. I spent 5 years as a regulatory affairs specialist focused on quality compliance at a CRO and a research site. Most recently I have served as an IRB project manager and IRB board member applying regulations and leading senior board members. My expertise is in supporting the regulatory aspects of clinical trials as well as protecting the well being of research subjects.