Jeremy Grise has been publishing, reviewing, and troubleshooting pharmaceutical regulatory submissions since 2006, during which time he’s worked on thousands of NDA, ANDA, IND, and DMF sequences. He has experience working with multiple publishing tools including EZsubs, Insight Publisher, and GlobalSubmit, and is comfortable in multiple document management systems including Veeva, Documentum, and SharePoint. In all environments, he has extensive experience producing high-quality, compliant eCTD submissions on time, frequently handling multiple submissions simultaneously. He has a track record of overcoming technical challenges while still meeting submission deadlines. He is experienced both as a team leader and individual contributor.
Jeremy Grise Regulatory Operations Specialist II