Checkout 0
Training Courses - Web Seminar Archives

Purchase the recording of a web seminar you have attended in the past and SAVE 50%! Contact Barnett Customer Service for details: +1 781.972.5400 or toll-free in the U.S. at 800.856.2556.

Web Seminar Archives provided through Barnett’s Learning Management System (Single User access) or by electronic file transfer (Site License).

Site license archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.

Bulk Archive access is available via Barnett’s Training Subscription. Click here to learn more.

Archive: Strategies for Effective Remote Monitoring

Course #: BI14218
June 1, 2020

Course Description

With the need to “shelter in place” and reduced social interactions due to the COVID-19 pandemic, it is more important than ever to look at ways to manage the conduct of clinical trials remotely, in real-time. Sites have had to modify strategies to manage patients in clinical trials and sponsors/CROs need to adapt quickly to meet obligations to the FDA and the general public to ensure trials are conducted under GCP. With sponsors/CROs focusing on expanding approaches to monitoring remotely, this web seminar will evaluate process and documentation, explore techniques for identifying issues at sites remotely, and examine the regulatory expectations for managing compliance. Better utilization of remote monitoring is critical to ensure sites are compliant and the data is accurate and consistent. Strategies for remote monitoring will be addressed, including the review of data trends, remote study management and communication, and “red flags” that may indicate issues on site.

Video Preview


Learning Objectives

  • Evaluate development of monitoring plans through protocol analysis for remote risk management
  • Discuss tools and risk evaluation approaches for remote monitoring
  • Explain techniques for practical corrective and preventive actions to ensure clear communication and resolution and documentation of issues

Who Should Attend

  • Clinical Research Associate Managers
  • Clinical Research Associates
  • Project Managers
  • Clinical Trial Managers
  • Study Coordinators


Nikki Christison, B.S., C.C.R.A., T.I.A.C.R.

Click here for complete trainer biographies


Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.