As a dedicated Regulatory Medical Writer with over five years of specialized experience in the pharmaceutical industry, I thrive on transforming complex clinical data into clear, impactful regulatory documents. I have authored over 30 documents across a myriad of phases and study designs including clinical study reports, protocols, and patient narratives serving as a lead or direct contributor.

Outside of my professional career, I am a wife and mom who enjoys spending time with family, making music, and welcoming international students through local outreach programs.