Webinar: Reimagining Clinical Trials & Improving Patient Safety with eSource Technology
Date: June 6th, 2023 from 1:00-2:00pm ET
Presenters: Takoda Roland (Sitero) and Megan Richards (CRIO), with webinar facilitator, Jonathan Andrus (CRIO)
Join us on Tuesday June 6th, 2023 for a webinar discussing how patient safety and overall trial execution can be improved by leveraging eSource technology to perform continuous monitoring in clinical trials. Sitero’s Takoda Roland, Director of Clinical Operations will be joined by CRIO’s Megan Richards, Customer Experience Manager. The webinar will be facilitated by Jonathan Andrus, President & COO of CRIO, a leading provider of eSource technology.
eSource technology has been around for over 10 years and has gained further mainstream adoption in a post-COVID world, however some sponsors are hesitant to adopt eSource technologies and continuous monitoring over the traditional data collection methods. On the other hand, many sites are already using solutions to run their research activities (including scheduling, CTMS, and eReg) and collecting the necessary protocol driven eSource data.
Today, sponsors require already overburdened research sites to use their systems and technology. By harnessing site collected eSource data, sponsors and CROs can benefit from streamlining clinical trial operations and improving patient safety. Further, with eSource technology, CRAs can carry out centralized, remote clinical data review and monitoring which frees up their time on site, to focus on patients and the critical aspects of clinical trial oversight.
The greatest benefit of eSource technology is the ability to access study data in real-time. Reducing the monitoring review timelines is essential for early risk and issue detection. Resolving issues in real-time enables corrective action for all patients, not just preventative action for future patients.
At the end of this webinar, attendees should have a better understanding of:
- How eSource allows for better clinical data
- What continuous monitoring is and how it’s used
- How continuous remote monitoring improves patient safety
About the presenters
Director of Clinical Operations | Sitero
Takoda has over 10 years of clinical research operations experience at various CROs. Throughout his career, Takoda has focused on maximizing the latest technology to streamline clinical trials, standardize data collection, and improve patient safety.
Manager, Customer Experience | CRIO
Megan has 5 years of clinical eSource operations experience, having been involved in many sponsor-driven eSource studies as well as countless site-based eSource implementations. Megan is committed to and manages the team responsible for ensuring customer success with CRIO’s solutions.
President and COO | CRIO
Jonathan has 27 years of industry experience and has been involved in all facets of the design, development, and deployment of clinical trial technologies having been in senior management positions in technology-enabled vendors. Jonathan is also engaged in initiatives aimed at improving and streamlining the clinical trial data collection process, including the decentralized trials and research alliance (DTRA), the Society for Clinical Data Management (SCDM), eCOA Consortium and frequently interacts with regulatory agencies and health authorities on topics in and around eSource and clinical trial execution.