Clinical research professional with over ten years experience in the pharmaceutical industry including clinical trials, drug safety, QC and editing of regulatory submission documents, and literature searches and reviews. Experience in many aspects of the drug development cycle, from word-smithing protocols to overseeing trial operations to QC of clinical study reports to global safety monitoring, has given me perspective of drug development and a variety of transferable skills. Strengths are program coordination, implementing a project from start to finish, bringing a written document to the necessary standard of accuracy and presentation, developing and training others in new processes, and accessing medical literature as a resource for solving current health issues and as a foundation for evidence-based practice. In addition, achieving my RN as a returning adult student has provided an in-depth understanding and appreciation of human health.