Alissa Threatt

PhD toxicologist with hands-on experience in nonclinical safety consulting and translational immunology research, specializing in the preparation and review of scientific and regulatory documentation supporting pharmaceutical and biotechnology development programs. As a Safety Consultant at SciLucent, I supported regulatory and scientific documentation for nonclinical development programs, working across cross-functional teams to synthesize complex data into clear, client-ready deliverables. My doctoral research further sharpened this ability, writing peer-reviewed publications, technical reports, and grant materials, and teaching graduate-level courses in toxicological metabolism, pathology, and regulatory toxicology. My scientific foundation spans in vivo and in vitro study design, immunotoxicology, and preclinical safety evaluation, giving me the technical depth to critically evaluate study data and communicate it accurately for regulatory, clinical, and scientific audiences. I'm looking for opportunities in medical writing, regulatory writing, and nonclinical consulting where I can combine scientific rigor with clear, audience-appropriate communication within biotech, pharma, CRO, or consulting environments. Core strengths: Nonclinical/regulatory documentation • Scientific & technical writing • Toxicology & risk assessment • Cross-functional collaboration • Data synthesis & interpretation