Principal Investigator Oversight and the Appropriate Delegation of Tasks

Oct 6, 2018, 18:21 PM
Course ID : 057
Acronym : PIT
Learn oversight and delegation best practices. Barnett International's course empowers PIs. Enroll now!

Course Description

Principal Investigators (PIs) are required to provide adequate oversight of all clinical research activities at the site, whether the activity is conducted by the PI, by study team members, or by applicable third parties. Adequate oversight encompasses many activities and obligations, such as ensuring regulatory compliance, staff training, and subject medical care. In this web seminar, we will discuss the regulatory requirements and guidance regarding adequate investigator oversight and appropriate delegation of study tasks, review documentation requirements, and determine strategies for appropriate delegation of tasks.

Learning Objectives

  • Recognize the industry concerns about adequate delegation and improper delegation of study activities
  • Identify documentation requirements for proper delegation and investigator oversight
  • Identify strategies for determining role assignment specific to a study project and requirements of PI oversight

Who Should Attend

  • Site Research Managers
  • Investigators
  • Clinical Research Associates/Monitors
  • Study/Clinical Research Associate Managers
  • Clinical Research Coordinators
  • Sponsors/CROs

Instructor

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

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#: 0778-0000-23-065-L99-P. Released: 9/23. 

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
  • Medical Device
Job Functions :
  • Clinical Operations & Trial Management
  • Clinical Quality Assurance
  • Clinical Research Associate
  • Clinical Research Coordinator
  • Clinical Research Investigator
  • Nursing
  • Project Manager
  • Quality Control
  • Regulatory Affairs
  • Study Site Compliance
  • Training
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