Loading…
← Back to schedule
Panel: Optimizing Clinical Trials Post-Pandemic Through Efficient Trial Design
Thursday September 26, 2024 5:00pm - 5:45pm EDT
  • Explore the evolving dynamics between clinical trial sponsors and research sites, focusing on remote operations and site access challenges post-COVID-19
  • Quantify the impact of protocol complexity on patient burden and site operations
  • Leverage data-driven approaches to streamline start-up activities, lower costs, and enhance enrollment efficiencies.
  • Discuss strategies for effective collaboration and relationship building, with an emphasis on integrating site and patient perspectives in protocol design
Speakers
VL

Victor Lucariello

Associate Director, Study Optimization, Bristol Myers Squibb
avatar for Suzanne Parker

Suzanne Parker

Vice President, Clinical Operations and Study Management, TuHURA Biosciences
Suzanne Parker is a pharmaceutical industry professional with over 25 years of experience leading teams through the various stages of the clinical development process from study concept, enrollment, reporting and health authority submissions in major global and emerging markets. Suzanne... Read More →
Thursday September 26, 2024 5:00pm - 5:45pm EDT
  Clinical Operations Track
  • Qtag clinicaloperationsfeaturedsession

Log in to save this to your schedule, view media, leave feedback and see who's attending!

Tweet Share
Share Modal

Share this link via

Or copy link