About Me

Scientific expertise that delivers data-driven, evidence-based medical communication.

I am a PhD-trained translational oncology scientist and medical writer, bringing hands-on research and clinical development experience in every project.

My scientific career began in translational oncology and advanced through postdoctoral research on cancer stem cells, intestinal regeneration, and rare pediatric cancers. I investigated disease mechanisms, chemoresistance, metastasis, and therapeutic response, resulting in seven peer-reviewed publications in leading journals, a review article, a book chapter, and multiple conference presentations. Notably, I presented first-author posters at AACR (2025 and 2026), with the 2025 abstract selected as late-breaking.

I transitioned to industry as a Senior Scientist in Translational Research and Clinical Development, focusing on biomarker development, clinical trials, pharmacology, and regulatory strategy. I led translational and clinical research programs in ctDNA-based biomarkers, GI oncology, and treatment-related peripheral neuropathy, contributing directly to clinical trial design, regulatory submissions, publications, and patents.

This dual background enables me to understand how science is generated, evaluated, and applied in research, clinical, regulatory, and commercial settings- not just write about it.

What this means for my clients

• I interpret evidence, not just summarize it

• Every claim I make is based on primary data, not secondary interpretation

• I craft narratives tailored to your specific communication objectives and targeted audience

• I write for research, clinical, regulatory, medical affairs, and commercial audiences

• I connect data to its broader clinical and development context to ensure content withstands expert scrutiny.

My goal is to make complex science clear and compelling while maintaining its accuracy and nuance.

If your next publication, submission, or presentation needs to withstand expert scrutiny, let's talk.