Building Relationships with Clinical Research Sites

Oct 6, 2018, 18:21 PM
Course ID : 109
Acronym : SRM
Join Barnett International's course of building relationships with clinical research sites. Avoid miscommunications and start having a thriving relationship today!

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.

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

The course will be led by one of the following instructors:

Janet Ellen Holwell, C.C.R.C., C.C.R.A., T.I.A.C.R., F.A.C.R.P.

Elizabeth Weeks-Rowe, LVN, C.C.R.A.

Click here for complete trainer biographies

Registration Fees

$735

Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.

Note: Due to COVID-19, we understand that most teams cannot currently dial-in together. As such, we are able to offer additional logins at a highly reduced rate. Please contact Barnett Customer Service at +1 781.972.5400 or toll-free in the U.S. 800.856.2556 to register with your additional participants requiring login credentials. Or email Customer Service at: customer.service@barnettinternational.com 

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation.  Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion.  ACPE#: 0778-0000-24-044-L99-P. Released: 8/24. 

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

Series :
  • Clinical Trials & Translational Medicine
Topics :
  • Clinical Research
  • Drug Safety & Development
  • Medical Device
Job Functions :
  • Clinical Operations & Trial Management
  • Clinical Quality Assurance
  • Clinical Research Associate
  • Project Manager
  • Study Site Compliance
  • Training
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