While Clinical IRT manages patient interactions and drug supplies as well as support reporting functions for trial sponsors, drug depots and investigative sites, it has the potential to do more. Through better planning and early engagement with experienced IRT specialists, you can reduce the risk, time and resources spent on your clinical trial.
What you will learn:
- Gain insights into how to better manage your clinical studies, how to optimize your trial for improved subject enrollment and inventory management
- Learn why earlier engagement with IRT planning specialists will improve outcomes for your study
- Learn the risks and challenges to avoid when planning your trial
- Learn what future developments are on the horizon for IRT to support clinical trials
Presented by Melissa Peirsel, IRT Manager, Sharp Clinical Services
As Manager of IRT Services at Sharp, a division of UDG Healthcare plc, Melissa is responsible for overseeing the successful development and maintenance of specific clinical trials utilizing features of IRT software. Melissa has over 10 years of clinical trial experience, as well as 8 years of experience managing technology systems in the military. Melissa has implemented and supported over 97 IRT studies over the course of her career and has particular expertise in oncology and pain management studies.