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COVID-19 Lessons Learned: Technology and Agility in the New Clinical Trial Landscape
Clinical trials research was forced to evolve and embrace technology in the wake of the COVID-19 pandemic. This unprecedented crisis created a necessary disruption in the use of technology to stand up clinical trials more quickly. But will sponsors, CROs, and sites revert to a “brick and mortar” standard by the end of the recovery? Or they seize the moment to adapt and implement technologies that add agility to the clinical trials process? Will the sense of urgency carry over to all clinical trials to boost enrollment regardless of COVID-19?
Join Advarra Chief Technology Officer and President of Technology Solutions, Jivan Achreja, Advarra Senior Vice President of Professional Services Orla Mester, and Forte Products Chief Product Officer James Wurdeman, for a fast look into the lessons learned of how clinical trials have been empowered by technologies at this critical juncture. Plus, gain a valuable perspective on how to enable a leap forward in transformative study activation.
- Focus on how a quick and nimble approach to data management, EDC, eRegulatory, and other solutions are enabling a jump to virtual and remote capabilities
- Bust implementation myths that halt initiatives to pursue clinical trial evolution
- Find out how technology and streamlined study activation services address the new needs for sites, sponsors, and CROs to work together for the benefit of patients and participants
CTO and President, Technology Solutions
SVP, Professional Services
Chief Product Officer, Forte Products
Who should watch?
Clinical research professionals involved in study startup and study conduct from sponsor, CRO, institutional, and site organizations. Specific takeaways for clinical operations managers, data managers, IT leadership, and procurement professionals.
The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.
If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements.
Certificate of Attendance
After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.
DATE: July 8, 2020
Time: 1 pm ET | 10 am PT
Duration: 1 hour