Julie has an extensive Pharma/Life Sciences background both working directly for Life Sciences companies as well as professional services firms for almost 20 years. She has consulted nationally and internationally to major pharmaceutical, biotechnology and devices organizations in the areas of strategic planning, industry best practice and implementation planning for pharmacovigilance process and systems, preclinical/clinical, regulatory affairs/risk mitigation, electronic document management, electronic submissions and labeling systems, program operations management and manufacturing functions. She has been involved in all phases of business process reengineering and technology planning, from strategy through implementation. Her expertise ranges from business and IT alignment to account management, business and product development.
Prior to joining Unisys, she was Director, eCOA Project Management for ERT; VP Global Delivery, Support and Platform for ArisGlobal responsible for global delivery of enterprise wide programs in clinical safety and regulatory affairs; was founder and lead of the HP Life Sciences Center of Excellence; as well as directed business and software development for a Midwest software company. In addition to several consulting engagements for large pharma, she was Director, Professional Services Western Region, at RWD Technologies, responsible for the regions account management and business development. Prior to RWD Technologies, she was Program Manager, eSubmissions, for Abbott Laboratories where she implemented a global, multilingual enterprise wide electronic submission system and the first industry integrated system for Structured Product Labeling (SPL) within the eSubmissions system.
Julie holds a patent, Genomic Sequencing for Clinical Trials, and has published several white papers, advertorial and PoVs. She has also presented at industry conferences such as IIR and KPMG and participated in PhRMA, HL7 working groups and the Pistoia Alliance.