About me
Have a doctorate in Molecular Biology and Biochemistry and completed a prestigious postdoctoral fellowship as a Michael J. Fox Fellow in Neuroscience. With over 11 years of experience as a scientific and regulatory writer, I have developed a diverse skill set in both publication and regulatory writing, particularly within the immunology and oncology therapeutic areas. Currently serving as the Safety Aggregate Report Process Subject Matter Expert, I strategically write and review submission documents in the drug development space, with a strong focus on impactful clinical to safety benefit-risk messaging. I am passionate about using AI tools to increase efficiencies and simplify processes in the field of regulatory writing.
