Medical and regulatory writer with 10+ years of scientific experience and 1.5 years of industry writing experience. I utilize my Ph.D. training to critically assess scientific literature and produce documents that support device marketing, regulation, and development. I have worked with medical device manufacturers to support evidence-based marketing or regulatory strategies and perform literature reviews to satisfy FDA and EU MDR requirements for clinical evaluation reports. I value communication, teamwork, organization, and attention to detail, and I can manage multiple projects and deadlines simultaneously.