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: Building Relationships with Clinical Research Sites

Course #: BI13420
March 20, 2019
WebSeminarArchive

Course Description

Relationships between sites and sponsors are often strained, and poor communication can interfere with having a productive study. Sites are contacted by multiple personnel during the study start-up process, and perhaps even during the study. By focusing on building relationships with the sites, the delays and errors in the startup and ongoing study process can be avoided. It is critical that the individuals working with the sites are in a position through training, knowledge, and support to positively reflect the sponsor and to ensure there is no gap in communication. This web seminar will focus on a variety of techniques for clinical study teams to use in building stronger relationships with the sites. Real-life scenarios and problem solving techniques will be discussed based on what can appear to be unreasonable monitor and sponsor requests to the site research staff.

Video Preview

 

Learning Objectives

  • Evaluate the study start-up process and build relationships right from the beginning
  • Implement advanced monitoring and communication techniques for Clinical Research Associates and staff interacting with the sites during the study
  • Utilize problem solving techniques based on a variety of real-life scenarios to allow sponsors/CROs and sites to work as partners during all phases of study execution

Who Should Attend

  • Study Coordinators
  • Site Regulatory Managers
  • Clinical Research Associate Managers
  • Clinical Research Associates
  • Principal Investigators
  • Site Managers

Instructor

Elizabeth Ronk Nelson, M.P.H.

Click here for complete trainer biographies

 

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

Training Portal Subscription Brochure