Sabrina is a Regulatory Medical Writer with 10+ years of experience combining deep scientific credibility, strong regulatory judgment, and a pragmatic approach to delivering high-quality documentation across all stages of clinical development. She has led and authored a broad range of regulatory documents across multiple indications, including oncology, inflammatory diseases, and biosimilars, with particular strength in Clinical Study Protocols and Reports, Briefing Documents, and Clinical Summaries and Overviews.
Her scientific foundation includes a PhD in human genetics, a postdoc in cancer research, and a Master’s in Drug Regulatory Affairs, giving her a strong ability to connect scientific evidence with regulatory expectations and to critically assess study design and data interpretation. In addition to her writing expertise, Sabrina is an experienced workshop leader who translates complex regulatory concepts into practical guidance, combining scientific rigor with pragmatic project management to strengthen team performance and regulatory readiness.