Webinar Registration
Flo & Tell Series: From Set-Up To Sign-Off, Best Practices for DOA and eLogs
Wednesday, April 15 @ 1 PM EST
Join us for a practical, peer-driven conversation about eLogs and Delegation of Authority (DOA) logs. We'll explore how sites approach setup, maintenance, and day-to-day use - including strategies teams use to encourage adoption and make logs part of their normal workflow. You'll hear what's working well, what's been tricky, and how sites keep logs inspection ready without overcomplicating the process.
Meet your Hosts
Erin Gainey
Senior Training Consultant
Florence Healthcare
Meet your Panelists
Matthew Johnson
Supervisor, Regulatory Affairs
Moffitt Cancer Center
Matthew Johnson is a clinical research leader with deep expertise in oncology trials and regulatory strategy. At Moffitt Cancer Center, he oversees protocol activation and regulatory startup for a wide range of studies, ensuring compliance, efficiency, and ethical rigor throughout the research lifecycle. His research career spans over 20 years, with roles in trial coordination, regulatory compliance, and mentorship across federally funded, investigator-initiated and industry-sponsored studies.
Dakota Gallimore
Regulatory Specialist
Cincinnati Children’s Hospital Medical Center
Dakota Gallimore is a Regulatory Specialist at Cincinnati Children’s Hospital Medical Center and serves as one of the Florence System Administrators for the institution and the NIH Rare Diseases Clinical Research Network Data Management and Coordinating Center (RDCRN DMCC). His work focuses on supporting compliant eISF workflows for FDA-regulated, investigator-initiated, and multi-site research, and leading Florence onboarding and training across hospital divisions and RDCRN consortia.
Chris Daniels
Clinical Research Data & Systems Analyst
Fred Hutchinson Cancer Center
Christopher Daniels is a Clinical Research Data and Systems Analyst at Fred Hutchinson Cancer Center, where he supports clinical trial regulatory operations through data tools and workflow design. He has extensive hands-on experience with Florence eBinders, building and managing training and delegation of authority eLogs across study teams. His focus is on creating practical systems that improve clarity and reduce administrative burden in clinical trials.