Decentralized Clinical Trials: Growing Trend? Tips and Best Practices for Sponsors/CROs
Although the concept of Decentralized Clinical Trials (DCTs) has been around for many years, COVID-19 has rapidly pushed the need for performing this type of trial to the forefront. Many sites and vendors have been struggling to keep up with the demand as well as the rapid implementation. Will this trend continue, and how can you as a sponsor get ahead of this curve? In this webinar we will discuss critical elements sponsors and CROs may want to consider before planning a decentralized trial, and if already doing so, methods to make the start-up and study conduct processes more efficient.
Attendees will learn:
- How recent trends and growth in decentralized Clinical Trials impacts sponsors and CROs – inclusive of vendor management and oversight
- Best practices for proactively building collaborative and compliant DCTs
- Proven tips for using technology and other solution to accelerate study start-ups and develop compliant and efficient study conduct processes
Director, Advarra Consulting
SVP, Advarra Consulting
Who should watch?
This content applies to anyone from sponsors/CROs organizations who may be involved in clinical trial oversight; director of clinical operations; clinical trial monitors; planning clinical trial timelines; clinical investigators; clinical project leaders; clinical trial management; clinical trial analysts as well as procurement directors and persons involved in vendor management and study plan design.
Attendance at this session has been approved for 1.00 contact hour of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.
Provider approved by the California Board of Registered Nursing, Provider Number 17600, for 1 contact hour. This documentation must be retained by the licensee for a period of 4 years after the course concludes.
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: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour