Lea Beaulieu

Background

About Lea Beaulieu

6+ years of industry program management experience, • Responsible for creating and managing cross-functional timelines and risks for drug development programs, including Discovery through IND-enabling phase of development• Proficient in Microsoft Office products (including Word, Excel, PowerPoint, Outlook, OneNote, SharePoint, Teams) and with Project Management Software Tools (including MSProject, SmartSheet, OnePager, WBS Schedule; Adobe Acrobat and PhotoShop)• Therapeutic and Platform Focus: hiPSC-derived cell therapy, hematology, autoimmune, immuno- oncology• Start-Up experience (i.e. seed-level through Series B), • Prepared and managed presentations and updates presented to the Board of Directors • Successful grant applications and funding by National Institute of Health (NHLBI, NIAID), DoD, MTEC, BARDA, and MLSC• Maintained license agreements with universities, research institutes, and biotech companies• Experience with IBC, IRB, and IACUC protocol development, compliance, and maintenance• Experience maintaining vendor relationships with academic centers, CROs, and government agencies• Completed 2020 Postgraduate Course in Clinical Pharmacology, Drug Development, and Regulation through Tufts Center for the Study of Drug Development and 2020 Leadership for Drug Development Teams Course through Tufts Center for the Study of Drug Development