Cameron Pierce

Cameron Pierce is a clinical development and regulatory affairs professional, providing regulatory and technical support in healthcare product development.  He specializes in regulatory project management, specifically for Investigational New Drug Applications (INDs) for filing to the United States (US) Food and Drug Administration (FDA).  Cameron has experience in various therapeutic areas and has managed and authored clinical and regulatory sections of INDs and New Drug Applications (NDAs) for submission, as well as clinical trial documentation, and has experience in the preparation, review, and publishing of electronic files for submission to the FDA.  He has also managed projects where he assisted clients in expanding their clinical program into the US after initiating clinical trials in other countries.  Previously Cameron provided technical, scientific, and regulatory support for nonclinical pharmacology and toxicology projects in multiple therapeutic areas.  He had provided support for outsourcing and study monitoring activities and nonclinical project management.  Cameron has a B.S. in Biology from George Mason University.