Ensuring Success Through Smarter Site Selection and Study Feasibility

Oct 6, 2018, 18:22 PM
Course ID : 160
Acronym : SSG
Site selection is a complex dance between sponsors and sites. The wrong choice can have serious consequences, impacting quality, time, and finances for both the sponsor and investigator. In this web seminar, the steps for site selection and study feasibility will be discussed. Sponsors will learn th

Course Description

Site selection is a complex dance between sponsors and sites. The wrong choice can have serious consequences, impacting quality, time, and finances for both the sponsor and investigator. In this web seminar, the steps for site selection and study feasibility will be discussed. Sponsors will learn the most critical questions to ask an investigator and staff to ensure quality and timely data as well as appropriate enrollment. Sites will learn how they can be proactive in the selection process and how to ensure the study is feasible. The process of site feasibility and selection will be outlined with key decision points for both sponsors and sites. Sites and sponsors will also learn what tools can help sites become “preferred” and achieve excellence. Tips for improving documentation and communication will be demonstrated through tools and worksheets, leading to successful collaboration between the site and sponsor and avoiding some common pitfalls. With careful consideration of placement of a clinical trial, learners can find success at closeout, audit, or inspection.

Learning Objectives

  • Discuss the steps in evaluating a site from both the sponsor and site perspectives
  • Identify the key questions to ask during a feasibility assessment/site visit
  • Explore how a site may become preferred by sponsors by implementing best practices

Who Should Attend

  • Clinical Research Coordinators
  • Investigators
  • Principal Investigators
  • Clinical Research Associates
  • Site Management Personnel

Instructor

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

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#: 0778-0000-20-033-L01-P. Released: 6/20. 

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
  • Project Management
Job Functions :
  • Clinical Operations & Trial Management
  • Clinical Research Associate
  • Project Manager
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