Increase Recruitment, Retention, and Compliance with Engaging Site Training
Informative and engaging site training materials are an important part of any clinical trial, especially during the study activation process. Traditionally, many training materials were produced and distributed on paper, including at in-person training events. Despite the increasingly remote conduct of clinical trials and widespread adoption of research technology, many sponsors, contract research organizations (CROs), and large academic institutions have yet to implement modern and effective training strategies.
Join us to learn how site training can impact your study’s success from recruitment, retention, compliance, and more. Explore best practices for eLearning, training, and virtual engagement from Marcus Miers, Advarra’s Director of Training, and Conor Flynn, Client Solutions Manager on Advarra’s Longboat Platform. Additionally, they will examine the current state of site training, critical industry trends, and strategies to implement at your organization.
- Examine the current state of site training across sponsors, CROs, and sites
- Discover industry trends impacting site training, such as decentralized trials, digital literacy, and adult learning, and how they pose threats and opportunities to your study’s success
- Outline sponsor, CRO, and site training responsibilities, and learn strategies to implement at your organization
- Review impactful and successful site training strategies across the clinical research lifecycle
Director of Client Training
Client Solutions Manager, Longboat Platform
Who should watch?
This content applies to research professionals representing sponsors, CROs, and institutions who are involved in the planning, development, and execution of clinical trials.
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: October 19, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour