Kimberly Kyle

Background

About Kimberly Kyle

Experienced Regulatory Professional with a demonstrated history of working in the Pharmaceutical industry including clinical trial development and filings, pediatric and adult in a variety of disease areas (oncology, ophthalmology, influenza, cystic fibrosis, hepatitis, rheumatoid arthritis, respiratory, Alzheimer's disease). My experience spans the drug development lifecycle (e.g, early, late development and post-marketing). I have experience building cross-functional consensus to produce ambitious regulatory strategies and high quality submissions. This includes producing lead regulatory filings to Health Canada, FDA, Swissmedic and EMA and planning rest of world filing waves. My genuine interest in the field keeps me motivated to stay on top of the ever changing regulatory landscape and I look forward to what technology will bring to what I do. I have also worked on internal strategic initiatives related to improving the efficiency of the regulatory submissions process from content to archiving including overall regulatory information and structured content management.