Training Program Title

Risk-Based Monitoring Clinical Trials

CTSA Hub Administered

no

Contact Information

Contact us by email at office@socra.org or by phone at 215-822-8644.

Training Program Description

Most site personnel have been exposed to the term risk based monitoring (RBM). But what is meant by RBM and where did the term come from? In addition to explaining the definition and rationale for RBM, this presentation will demonstrate how it will be implemented by clinical trial Sponsors and what the downstream effects will be to sites. Lastly, the presentation will provide insight into what sites need to do to best prepare for this new monitoring paradigm.

This is a 60 minute internet media player video of a voice over slide show.
A quiz concluding the presentation will summarize the topic and evaluate your understanding of the material.

Competency Keywords

Audits

Other Keywords

Risk Based Monitoring (RBM)

Digital Commons Disciplines

Medical Education

Public

yes

Cost to Access

yes

Learning Objectives

At the completion of the webinar, participants should be able to:

  • Understand the rationale for changing the fundamentals of the clinical trial monitoring process
  • Describe what is Risk Based Monitoring in Clinical Trials
  • Recognize how Risk Base Monitoring will affect the clinical trial Site.
  • Identify current Site processes that will need to be altered to accommodate clinical trials Risk Based Monitoring

Delivery Method

Online

Target Learners

Clinical Research Professionals (other than PI)

Learning Level

Skilled

Onboarding

no

Frequency

On demand

Time Needed

60 minutes

Associated Assessment

yes

Assessment Methods

Learning outcomes

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