Contract/Freelance Clinical Research Scientist/Medical Writer and AI enthusiast specializing in clinical regulatory and scientific communications documents for the pharmaceutical and biotechnology industry. With nearly 20 years in the pharmaceutical industry, Frank specializes in regulatory and scientific communications documents, where he delivering impactful materials tailored for regulatory authorities, healthcare professionals, and patients. Frank's expertise spans clinical and regulatory documents, including Health Authority Response Letters, Briefing Documents, supplemental New Drug Applications, and Clinical Study Reports, with a focus on oncology and healthcare economics. He excels in distilling complex scientific data into clear, actionable insights to support key regulatory submissions and clinical trial outcomes and has been involved in numerous submissions.